ACOT7 |
protein-coding |
32469171 |
qRT-PCR |
tissue |
China |
10 |
10 |
Up |
- |
No Reports |
Upregulated in gastric tumor tissues and GC cell lines.Furthermore, NMRAL2P was downregulated in tumor tissues and GC cell lines. |
target/prognosis |
0.025 |
- |
- |
ACOT7 |
protein-coding |
32469171 |
Cell proliferation assay;Migration assay;Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
ACOT7 gene silencing induced a less malignant phenotype and was closely correlated to reduced cell proliferation and migration, altered cell cycle, and increased apoptosis. |
target/prognosis |
0.025 |
- |
- |
ACOT7 |
protein-coding |
32469171 |
Western blot |
tissue |
China |
5 |
5 |
Up |
- |
No Reports |
Upregulated in GC tumor tissue at protein level |
target/prognosis |
0.025 |
- |
- |
ACOT7 |
protein-coding |
32469171 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
NMRAL2P indirectly methylated ACOT7 by binding to DNMT3b, thereby suppressing ACOT7 expression. |
target/prognosis |
0.025 |
- |
- |
ACTN4 |
protein-coding |
28581489 |
qRT-PCR |
tissue |
China |
47 |
47 |
Up |
Up |
No Reports |
Upregulated in GC Tissue Samples |
target |
- |
- |
- |
ACTN4 |
protein-coding |
28581489 |
Western blot |
cell line |
- |
- |
- |
Up |
- |
No Reports |
Upregulated in GC Cell Lines |
target |
- |
- |
- |
ACTN4 |
protein-coding |
28581489 |
Adhesion assay;Migration assay;Invasion assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Downregulation of Actn4 enhances GC cell adhesion, suppresses migration and invasion of GC Cells |
target |
- |
- |
- |
ADAM9 |
protein-coding |
28260063 |
qRT-PCR |
tissue |
China |
76 |
76 |
Up |
- |
No Reports |
The expression of ADAM9 was significantly correlated with patient clinicopathological features including tumor size, local invasion, lymph node metastasis and TNM stage. |
target |
- |
- |
- |
ADAM9 |
protein-coding |
28260063 |
IHC; Western blot |
tissue |
China |
76 |
76 |
Up |
- |
No Reports |
ADAM9 is expressed frequently higher in GC tissues when compared with adjacent non-cancerous tissues |
target |
- |
- |
- |
ADAM9 |
protein-coding |
28260063 |
Cell proliferation assay; Cell cycle analysis. |
cell line |
- |
- |
- |
- |
- |
No Reports |
|
target |
- |
- |
- |
ADAM9 |
protein-coding |
28260063 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
ADAM9 is a direct target post-transcriptionally regulated by miR-126 in GC cells. |
target |
- |
- |
- |
ADRM1 |
protein-coding |
24968865 |
Cell proliferation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpression of Adrm1 promoted cell proliferation of conditionally-immortalized, mouse ImSt gastric epithelial cells, with increased S1 phase fraction and decreased expression of p21(Cip1). These results collectively indicate that ADRM1 promoted gastric epithelial cell proliferation by cell cycle progression |
target |
- |
- |
- |
ADRM1 |
protein-coding |
24968865 |
Comparative genomic hybridization |
tissue |
Korea |
32 |
- |
- |
- |
No Reports |
ADRM1 was the third most frequent target for gene amplification |
target |
- |
- |
- |
ADRM1 |
protein-coding |
24968865 |
Microarray |
tissue |
Korea |
32 |
21 |
Up |
- |
No Reports |
ADRM1 was also overexpressed in 92 cancer patients than in 21 healthy volunteers |
target |
- |
- |
- |
AFAP1L2 |
protein-coding |
24387290 |
Clonogenic assay; Soft agar colony-forming assay; Flow cytometry; BrdU incorporation assay; Cell viability assay; Invasion and migration assay; Xenograft model |
cell line |
- |
- |
- |
- |
- |
No Reports |
The proliferation, migration, and invasion of GC cell lines were all significantly inhibited by knockdown of XB130. In a xenograft model, tumor growth was markedly inhibited after shXB130-transfected GC cells were implanted into nude mice. After XB130 knockdown, GC cells showed a more epithelial-like phenotype. Silencing of XB130 reduced the expression of p-Akt/Akt, upregulated expression of epithelial markers including E-cadherin, aβ-catenin and β-catenin, and downregulated mesenchymal markers including fibronectin and vimentin. |
target |
- |
- |
- |
AGER |
protein-coding |
24441189 |
IHC |
tissue |
China |
40 |
40 |
Up |
- |
No Reports |
RAGE was highly expressed in cancer tissues, and correlated with lymph node metastases. |
target |
- |
- |
- |
AGER |
protein-coding |
24441189 |
Cell proliferation assay; Invasion and migration assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
Knockdown of RAGE reduced cell proliferation and invasion of gastric cancer with decreased expression of AKT, PCNA and MMP-2, and induced cell apoptosis and cycle arrest |
target |
- |
- |
- |
AKT3 |
protein-coding |
29228422 |
qRT-PCR |
tissue |
China |
42 |
42 |
Up |
- |
No Reports |
AKT3 was up-regulated in GC tissues when compared with matched normal tissues. |
target |
- |
- |
- |
AKT3 |
protein-coding |
29228422 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
AKT3 was chosen as the target gene of miR-582-5p. Moreover, restoration of AKT3 could impair tumor suppression role of miR-582-5p on gastric cancer growth. |
target |
- |
- |
- |
ANGPTL6 |
protein-coding |
31146977 |
qRT-PCR |
cell line |
- |
- |
- |
- |
- |
No Reports |
ANGPTL6 was overexpressed in Alpha-fetoprotein (AFP)-producing gastric cancer (AFPGC) cell lins compared to that of common gastric cell lines; A high level of ANGPTL6 confers a poor prognosis and is correlated with the expression of CD34 (an endothelial cell marker). |
target |
- |
- |
- |
ANGPTL6 |
protein-coding |
31146977 |
HUVEC tube formation assay; HUVEC proliferation assay; Invasion and migration assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
ANGPTL6 promotes endothelial cell migration and tube formation, Moreover, ANGPTL6 knockdown inhibits cancer cell apoptosis and invasiveness. Mechanistically, ANGPTL6 activates the ERK1/2 and AKT pathways. Treatment of ERK1/2 or AKT inhibitor can attenuated cell migration and tube formation. |
target |
- |
- |
- |
ANGPTL6 |
protein-coding |
31146977 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
ANGPTL6 loss results in tumor growth in vivo. |
target |
- |
- |
- |
ANKRD40CL |
protein-coding |
32293550 |
qRT-PCR |
tissue |
China |
30 |
30 |
Up |
- |
No Reports |
LINC00483 level was increased in gastric cancer tissues and cells. . Besides, inhibition of LINC00483 decreased xenograft tumor growth by regulating miR-490-3p/MAPK1 axis. |
target |
- |
- |
- |
ANKRD40CL |
protein-coding |
32293550 |
Cell viability assay; Invasion and migration assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
Knockdown of LINC00483 inhibited cells viability, migration and invasion but promoted apoptosis in gastric cancer cells. |
target |
- |
- |
- |
ANKRD40CL |
protein-coding |
32293550 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
LINC00483 could increase MAPK1 expression by competitively sponging miR-490-3p. miR-490-3p overexpression suppressed gastric cancer development, which was abated by introduction of LINC00483 |
target |
- |
- |
- |
ANKRD40CL |
protein-coding |
32293550 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
Knockdown of LINC00483 decreases tumor growth in gastric cancer xenograft model. |
target |
- |
- |
- |
ASCL2 |
protein-coding |
29746925 |
qRT-PCR |
tissue |
China |
24 |
24 |
Up |
- |
No Reports |
The mRNA levels of ASCL2 were significantly increased in GC tissues compared to ad- jacent non-tumor gastric epithelium; ASCL2 expression in GC correlated with poor histological differentiation, tumor cell invasion into lymph nodes, and higher TNM stages (III + IV). SMYD3 expression status correlates with ASCL2 in GC tissues. |
target/prognosis |
< 0.001 |
- |
- |
ASCL2 |
protein-coding |
29746925 |
IHC |
tissue |
China |
- |
- |
- |
- |
No Reports |
ASCL2 protein were detected in the nuclei of GC cells |
target/prognosis |
< 0.001 |
- |
- |
ASCL2 |
protein-coding |
29746925 |
qRT-PCR; FACS; Tumorsphere formation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
ASCL2+ cells showed increased propensity of growing as tumorspheres |
target/prognosis |
< 0.001 |
- |
- |
ASCL2 |
protein-coding |
29746925 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
High levels of ASCL2 expression are necessary for stemness and tumorigenicity of ASCL2+ GC cells |
target/prognosis |
< 0.001 |
- |
- |
ASCL2 |
protein-coding |
29746925 |
ChIP-qPCR |
cell line |
- |
- |
- |
- |
- |
No Reports |
SMYD3 maintains high H3K4me3 levels on the ASCL2 promoter in ASCL2+ cells, indicating its potential role in regulating ASCL2 transcription and expression. |
target/prognosis |
< 0.001 |
- |
- |
ASCL2 |
protein-coding |
29746925 |
qRT-PCR; Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
Depletion of SMYD3 inhibits Wnt-induced upregulation of ASCL2. |
target/prognosis |
< 0.001 |
- |
- |
ASCL2 |
protein-coding |
30106147 |
qRT-PCR:Western blot; IHC |
tissue |
China |
32 |
32 |
Up |
- |
No Reports |
Expression of ASCL2 is highest in metastases, among adjacent normal tissues, primary gastric tumors and gastric metastases. |
target |
- |
- |
- |
ASCL2 |
protein-coding |
30106147 |
Cell invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
ASCL2 expression contributes to cell migration and invasion in GC cells. |
target |
- |
- |
- |
ASCL2 |
protein-coding |
30106147 |
Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
the expression of E-cadherin in ASCL2-overexpressing cell lines decreased, while Zeb-1, twist-related protein 1 (Twist), Integrin, Vimentin, 72 kDa type IV collagenase (MMP-2) and matrix metalloproteinase 9 (MMP-9) were upregulated in ASCL2-overexpressing cell lines |
target |
- |
- |
- |
ASCL2 |
protein-coding |
30106147 |
Luciferase reporter assay; ChIP |
cell line |
- |
- |
- |
- |
- |
No Reports |
ASCL2 may interact with the promoter of pre-miR223, and inhibit the maturation of miR223. |
target |
- |
- |
- |
BAG3 |
protein-coding |
30514177 |
qRT-PCR; Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
BAG3 mRNA and protein levels were increased following treatment with HGF. HGF-mediated BAG3 upregulation increased cell proliferation and cell invasion; however, it decreased apoptosis. HGF-mediated BAG3 upregulation is regulated by an ERK and Egr1-dependent pathway. BAG3 may have an important role in HGF-mediated cell proliferation and metastasis in gastric cancer through an ERK and Egr1-dependent pathway. |
target |
- |
- |
- |
BAG3 |
protein-coding |
30514177 |
Cell proliferation assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
HGF-mediated BAG3 upregulation increased cell proliferation and cell invasion; however, it decreased apoptosis. |
target |
- |
- |
- |
BRD4 |
protein-coding |
29434197 |
IHC |
tissue |
China |
52 |
52 |
Up |
- |
No Reports |
BRD4 is highly overexpressed in gastric cancer tissues. |
target |
- |
- |
- |
BRD4 |
protein-coding |
29434197 |
Cell proliferation assay; Invasion and migration assay; |
cell line |
- |
- |
- |
- |
- |
No Reports |
The BET inhibitor JQ1 inhibits gastric cancer cell proliferation by inducing cellular senescence. BRD4 is involved in JQ1-induced cellular senescence. |
target |
- |
- |
- |
BRD4 |
protein-coding |
29434197 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
BRD4 regulates the 3′-UTR of p21. mRNA CDKN1A |
target |
- |
- |
- |
BRD4 |
protein-coding |
29434197 |
CHIP assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
BRD4, together with E2F1, regulates miR-106b-5p transcription and cellular senescence. |
target |
- |
- |
- |
BTG1 |
protein-coding |
26050197 |
RT-PCR; Western blot; MS-PCR |
cell line |
- |
- |
- |
- |
- |
No Reports |
BTG1 protein expression (19 kDa) was detectable in gastric cancer and epithelial cell lines; BTG1 mRNA was high expressed in cancer and epithelial cells and a decreased level of methylation of BTG1 after treated with 5-Aza-dC. |
target/prognosis |
0.047 |
- |
- |
BTG1 |
protein-coding |
26050197 |
Cell proliferation assay; Invasion and migration assays; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
BTG1 overexpression suppressed tumor growth and lung metastasis of gastric cancer cells. |
target/prognosis |
0.047 |
- |
- |
BTG1 |
protein-coding |
26050197 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
BTG1 overexpression enhanced autophagy and apoptosis in xenograft models. |
target/prognosis |
0.047 |
- |
- |
BTG1 |
protein-coding |
26050197 |
RT-PCR |
tissue |
Japan |
613 |
577 |
Down |
- |
No Reports |
BTG1 expression was statistically lower in gastric cancer than non-neoplastic mucosa and metastatic cancer in lymph node. BTG1 expression was positively correlated with depth of invasion, lymphatic and venous invasion, lymph node metastasis, TNM staging and worse prognosis. The diffuse-type carcinoma showed less BTG1 expression than intestinal- and mixed-type ones. |
target/prognosis |
0.047 |
- |
- |
BTG3 |
protein-coding |
25904053 |
Western blot; IHC |
tissue |
Japan |
38 |
38 |
Down |
- |
No Reports |
BTG3 expression was decreased in gastric cancer in comparison to the adjacent mucosa, and positively correlated with venous invasion and dedifferentiation of cancer. |
target |
- |
- |
- |
BTG3 |
protein-coding |
25904053 |
Cell proliferation assay; Invasion and migration assays; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
BTG3 overexpression inhibited proliferation, induced S/G2 arrest, differentiation, autophagy, apoptosis, suppressed migration and invasion |
target |
- |
- |
- |
BTG3 |
protein-coding |
25904053 |
qRT-PCR; Cell transfection |
cell line |
- |
- |
- |
- |
- |
No Reports |
BTG3 transfectants showed a higher mRNA expression of p27, Bax, 14-3-3, Caspase-3, Caspase-9, Beclin 1, NF-κB, IL-1, -2, -4, -10 and -17, but a lower mRNA expression of p21, MMP-9 and VEGF than the control and mock;exposed to cisplatin (DDP), MG132, paclitaxel, and SAHA, BTG3 transfectants showed a lower viability and a higher apoptotic level than the control in both concentration and time-dependent manners |
target |
- |
- |
- |
BTG3 |
protein-coding |
25904053 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
BTG3 suppresses the growth of gastric cancer cells in nude mice. |
target |
- |
- |
- |
BTG3 |
protein-coding |
25238703 |
qRT-PCR; Western blot |
tissue |
China |
18 |
18 |
Down |
- |
No Reports |
BTG3 was obviously down-regulated in GC tissues. |
target/prognosis |
0.001 |
- |
- |
BTG3 |
protein-coding |
25238703 |
IHC |
tissue |
China |
131 |
131 |
- |
- |
No Reports |
The expression of BTG3 was obvi- ously lower in GC tissues than adjacent gastric mucosa. Its expression was positively correlated with distant metastasis. Patients with lower BTG3 expression had shorter overall survival time. |
target/prognosis |
0.001 |
- |
- |
BTG3 |
protein-coding |
25238703 |
Cell proliferation assay; Invasion and migration assays; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
BTG3 suppressed the proliferation of GC cells in vitro. It also inhibited migration and invasion of GC cells in vitro. |
target/prognosis |
0.001 |
- |
- |
BTG3 |
protein-coding |
25238703 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
BTG3 suppressed the proliferation of GC cells in vivo. |
target/prognosis |
0.001 |
- |
- |
C1QTNF6 |
protein-coding |
30431096 |
Gene microarray |
tissue |
China |
64 |
64 |
Up |
- |
No Reports |
C1QTNF6 was up-regulated in GC tissues. |
target |
- |
- |
- |
C1QTNF6 |
protein-coding |
30431096 |
IHC |
tissue |
China |
52 |
52 |
Up |
- |
No Reports |
C1QTNF6 was primarily expressed in the cytoplasm and exhibited a diffuse granular distribution. The expression rate of C1QTNF6 in GC tissues was significantly higher than that in the normal gastric tissues |
target |
- |
- |
- |
C1QTNF6 |
protein-coding |
30431096 |
Cell proliferation assay; Invasion and migration assays; Flow cytometry; Cell colony formation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Interference of C1QTNF6 expression influenced the proliferation, migration and invasion ability of Gc cells in vitro. |
target |
- |
- |
- |
CACUL1 |
protein-coding |
24004834 |
qRT-PCR; IHC |
tissue |
China |
43 |
43 |
Up |
Up |
Related |
CACUL1 was highly expressed in gastric cancer tissues and negatively correlated with gastric cancer differentiation and TNM stage. In addition, CACUL1 expression was high in H.pylori-infected tissues compared with H.pylori non-infected tissue. |
target |
- |
- |
- |
CASK |
protein-coding |
25373785 |
qRT-PCR |
tissue |
China |
50 |
50 |
Down |
- |
Related |
CASK was over-expressed in tumors and H. pylori positive tissues and its mRNA levels were inversely correlated with miR-203 expression |
target |
- |
- |
- |
CCAT1 |
lncRNA |
28535628 |
qRT-PCR |
tissue |
China |
62 |
62 |
Up |
- |
No Reports |
The expressions of CCAT1 mRNA in GC tissues were significantly higher than in the normal tissues.The expression of CCAT1 varied significantly among patients with different TNM stage, depth of invasion, and lymph node metastasis. |
target |
- |
- |
- |
CCAT1 |
lncRNA |
28535628 |
Cell proliferation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Down-regulation of CCAT1 in MGC-803 and SGC-7901 cells significantly inhibited the cell proliferation. |
target |
- |
- |
- |
CCEPR |
lncRNA |
29771412 |
qRT-PCR |
tissue |
China |
77 |
77 |
Up |
- |
No Reports |
Expression of lncRNA CCHE1 in the tumor cell lines was increased (p<0.05).Bcl-2 protein expression increased, but Bax protein expression decreased in lncRNA CCHE1 upregulation group (p<0.05); the effect was reversed in lncRNA CCHE1 down-regulation group (p<0.05). |
target |
- |
- |
- |
CCEPR |
lncRNA |
29771412 |
Cell proliferation assay; Cell colony formation assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
Down-regulated lncRNA CCHE1 decreased proliferative activity and colony formation capacity.Cell cycle was promot_x005fed in lncRNA CCHE1 up-regulation group. |
target |
- |
- |
- |
CCKBR |
protein-coding |
27518872 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Cholecystokinin B receptor (CCK-BR) was a direct target of miR-148a. |
target |
- |
- |
- |
CCKBR |
protein-coding |
27518872 |
Cell proliferation assay; Cell migration assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
siRNA-induced knockdown of CCK-BR elicited similar anti-oncogenic effects (decreased proliferation and migration) as those induced by enforced miR-148a expression. |
target |
- |
- |
- |
CD151 |
protein-coding |
23533596 |
qRT-PCR; Western blot |
tissue |
China |
20 |
20 |
Up |
- |
No Reports |
CD151 mRNA and protein expression was increased in HGC tissues and HGC cells than in nontumor tissues and HGEC cells. CD151 overexpression was significantly correlated with high TNM stage, depth of invasion and positive lymph node involvement (p<0.05), and Importantly, the postoperative 5-year overall survival of patients with CD151(low) and/or integrin a3(low) was higher than that of patients with CD151(high) and/or integrin a3(high). |
target/prognosis |
0.007 |
- |
- |
CD151 |
protein-coding |
23533596 |
IHC |
tissue |
China |
76 |
- |
- |
- |
No Reports |
CD151 protein immunoreactivity localized to the cell membrane. High expression of CD151 was significantly correlated with tumor size (p = 0.021), depth of invasion (p = 0.004), lymph node involvement (p =0.028) and high tumor stage (p = 0.002). Overexpression of CD151 are Independent Factors Predicting the Prognosis of HGC Patients. |
target/prognosis |
0.007 |
- |
- |
CD151 |
protein-coding |
23533596 |
Cell proliferation assay; Invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
Down-regulation of CD151 by vshRNA-CD151 impaired metastasis and invasion of HGC-27 cells, but did not affect cell proliferation. CD151-cDNA transfection rescued the metastatic potential and invasiveness of HGC-27-vshCD151 cells, but not those of HGC-27-vshintegrin a3 cells in vitro. |
target/prognosis |
0.007 |
- |
- |
CD151 |
protein-coding |
23533596 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
CD151 Promoted Metastasis of HGC Cells in vivo |
target/prognosis |
0.007 |
- |
- |
CD151 |
protein-coding |
23533596 |
Co-ip assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
CD151 formed a complex with integrin a3 in HGC cells. |
target/prognosis |
0.007 |
- |
- |
CD276 |
protein-coding |
25120098 |
qRT-PCR |
tissue |
China |
32 |
32 |
Up |
- |
No Reports |
B7-H3 expression was significantly higher in the gastric cancer group than that in the normal gaster group. |
target |
- |
- |
- |
CD276 |
protein-coding |
25120098 |
IHC |
tissue |
China |
32 |
32 |
Up |
- |
No Reports |
B7-H3 expression was significantly higher in the gastric cancer group than that in the normal gaster group. |
target |
- |
- |
- |
CD276 |
protein-coding |
25120098 |
Cell invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
B7-H3 knockdown by RNA interference decreased cell migration and Transwell invasion up to 50% in vitro. |
target |
- |
- |
- |
CD276 |
protein-coding |
25120098 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
B7-H3 expression reduced gastric cancer metastasis in vivo。 |
target |
- |
- |
- |
CDC42 |
protein-coding |
26549550 |
Cell proliferation assay; Invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
Knockdown of CDC42 significantly inhibited the proliferation of AGS and SGC7901 cells, and it was suggested that this inhibitory process may be due to cell cycle arrest at G1/S phase and downregulation of cyclin A, cyclin D1, cyclin E and proliferating cell nuclear antigen. Furthermore, knockdown of CDC42 markedly inhibited the migration and invasion of GC cells, and suppressed the expression of matrix metalloproteinase 9 |
target |
- |
- |
- |
CDK9 |
protein-coding |
28701053 |
qRT-PCR |
tissue |
China |
52 |
52 |
Up |
- |
No Reports |
CDK9 was upregulated in gastric cancer and the CDK9 expression levels were inversely correlated with that of miR-613 in gastric cancer tissues. |
target |
- |
- |
- |
CDK9 |
protein-coding |
28701053 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
CDK9 is a direct target of miR-613 in gastric cancer |
target |
- |
- |
- |
CDKL1 |
protein-coding |
22369697 |
IHC |
tissue |
China |
66 |
66 |
Up |
- |
No Reports |
High expression of CDKL1 protein was observed in gastric cancer tissues compared with matched adjacent tissues. Furthermore, we show that the reduction of CDKL1 with its siRNA stimulates the activation of Bcl-2-interacting killer (Bik) pro-apoptotic protein and attenuated the expression of proliferating cell nuclear antigen PCNA. |
target |
- |
- |
- |
CDKL1 |
protein-coding |
22369697 |
Cell proliferation assay; Cell invasion and migration assays; Cell colony forming assay; |
cell line |
- |
- |
- |
- |
- |
No Reports |
Loss of CDKL1 function in both SGC7901 and MGC-803 gastric cancer cells significantly decreases cellular proliferation and increases apoptosis (p < 0.01). |
target |
- |
- |
- |
CDKN2B-AS1 |
lncRNA |
31242038 |
PCR |
tissue |
China |
192 |
- |
- |
- |
No Reports |
Patients with higher ANRIL survived worse. Expressions of TET2 and ANRIL were negatively correlated in the patient samples. |
target/prognosis |
< 0.001 |
- |
- |
CDKN2B-AS1 |
lncRNA |
31242038 |
Apoptosis assay; Migration assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
ANRIL suppresses apoptosis in gastric cancer cell, enhances metastasis |
target/prognosis |
< 0.001 |
- |
- |
CDKN2B-AS1 |
lncRNA |
31242038 |
Xenograft tumor mouse model |
cell line |
- |
- |
- |
- |
- |
No Reports |
ANRIL promotes tumor growth in vivo |
target/prognosis |
< 0.001 |
- |
- |
CDKN2B-AS1 |
lncRNA |
30156609 |
qRT-PCR |
tissue |
China |
20 |
20 |
Up |
- |
No Reports |
ANRIL level was elevated in gastric cancer tissues and cell lines. Furthermore, ANRIL silence down-regulated BMI1 via up-regulating miR-99a. BMI1 silence down-regulated Bcl-2 and key kinases in the Notch and mTOR pathways and up-regulated p16 and cleaved caspases. |
target |
- |
- |
- |
CDKN2B-AS1 |
lncRNA |
30156609 |
Cell proliferation assay; Invasion and migration assays; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
Knockdown of ANRIL suppressed cell viability, migration, and invasion, and increased apoptosis through up-regulating miR-99a. |
target |
- |
- |
- |
CDKN2B-AS1 |
lncRNA |
30156609 |
qRT-PCR; Cell transfection |
cell line |
- |
- |
- |
- |
- |
No Reports |
ANRIL silence_x005finduced up-regulation of miR-99a was significantly reversed by miR-99a inhibitor.ANRIL knockdown down-regulated the expression of BMI1 by modulating miR-99a in gastric cancer cells in vitro |
target |
- |
- |
- |
CEMIP |
protein-coding |
28422983 |
qRT-PCR |
tissue |
China |
321 |
- |
- |
- |
No Reports |
KIAA1199 was upregulated in GC tissue and was an essential independent marker for poor prognosis. KIAA1199 mRNA expression was correlated with the clinical characteristics regarding depth of invasion (T-staging), distant metastasis (M-staging) and TNM staging of GC patients. |
target/prognosis |
< 0.001 |
- |
- |
CEMIP |
protein-coding |
28422983 |
IHC |
tissue |
China |
123 |
- |
- |
- |
No Reports |
KIAA1199 protein expression was highly expressed in the cytoplasm of GC tissue cells and was correlated with depth of invasion, lymph node status (N-staging), metastasis and TNM staging |
target/prognosis |
< 0.001 |
- |
- |
CEMIP |
protein-coding |
28422983 |
Cell proliferation assay; Cell invasion and migration assays; Cell colony formation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Knockdown KIAA1199 suppressed the proliferation, migration and invasion in GC cells. KIAA1199 stimulated the Wnt/β-catenin signaling pathway and the enzymatic activity of matrix metalloproteinase (MMP) family members and thus accelerated the epithelial-to-mesenchymal transition (EMT) progression in GC cells. |
target/prognosis |
< 0.001 |
- |
- |
CLCN3 |
protein-coding |
30217218 |
IHC |
tissue |
China |
90 |
90 |
Up |
- |
No Reports |
CLC-3 was overexpressed in human GC tissues and that overexpression of CLC-3 was a poor prognostic biomarker for GC patients (P = 0.012). Higher expression of CLC-3 was correlated with deeper tumor invasion (P = 0.006) and increased lymph node metastasis (P = 0.016) |
target/prognosis |
0.012 |
- |
- |
CLCN3 |
protein-coding |
30217218 |
Cell proliferation assay; Cell invasion and migration assays; |
cell line |
- |
- |
- |
- |
- |
No Reports |
Knockdown of CLC-3 inhibited cell proliferation and migration in vitro. |
target/prognosis |
0.012 |
- |
- |
CLCN3 |
protein-coding |
30217218 |
Luciferase reporter assay;ChIP assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
XRCC5 was identified as a CLC-3 promoter-binding protein, and both CLC-3 and XRCC5 were prognostic factors of overall survival in GC patients. |
target/prognosis |
0.012 |
- |
- |
CLCN3 |
protein-coding |
30217218 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
The expression and function of CLC-3 were regulated by XRCC5 in vivo |
target/prognosis |
0.012 |
- |
- |
CLDN18 |
protein-coding |
24647998 |
Western blot |
tissue |
China |
45 |
45 |
Down |
Down |
No Reports |
Claudin-18 was downregulated in tumor tissues with larger tumor size, intestinal histologic type, deeper local invasion and more advanced TNM stage. |
target |
- |
- |
- |
CLDN18 |
protein-coding |
24647998 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-1303 could bind to the putative binding sites in CLDN18 mRNA 3'-UTR and visibly lower the expression of claudin-18. The introduction of claudin-18 without 3'-UTR restored the miR-1303 promoting migration function. |
target |
- |
- |
- |
CLEC4M |
protein-coding |
28403883 |
ELISA assay |
serum |
China |
207 |
197 |
Up |
Up |
No Reports |
DC-SIGNR serum level was significantly increased in gastric cancer patients compared with healthy group. DC-SIGNR level was associated with an advanced pathological stage in gastric cancer patients. |
target |
- |
- |
- |
CLEC4M |
protein-coding |
28403883 |
Cell proliferation assay; Cell invasion and migration assays; Cell colony formation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
DC-SIGNR knockdown inhibited the proliferation, migration and invasion of gastric cancer cells in vitro and DC-SIGNR overexpression promoted cell proliferation, migration and invasion. |
target |
- |
- |
- |
CLEC4M |
protein-coding |
28403883 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
DC-SIGNR knockdown suppressed the liver metastasis in vivo. |
target |
- |
- |
- |
COPS7A |
protein-coding |
31409899 |
qRT-PCR |
tissue |
China |
84 |
29 |
Down |
- |
No Reports |
A significant decreased expression of COPS7A at mRNA levels in GC tissues compared with the non_x005ftumorous gastric tissues |
target |
- |
- |
- |
COPS7A |
protein-coding |
31409899 |
IHC |
tissue |
China |
84 |
29 |
Down |
- |
No Reports |
A significant decreased expression of COPS7A at protein levels in GC tissues compared with the non_x005ftumorous gastric tissues. Lower COPS7A expression was found to be associated with larger tumor size and positive lymph node metastasis. |
target |
- |
- |
- |
COPS7A |
protein-coding |
31409899 |
RNA pull-down assay; RIP; Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
KRT19P3 could bind COPS7A directly and might regulate COPS7A activity in GC |
target |
- |
- |
- |
CRK |
protein-coding |
25027343 |
Cell proliferation assay; Cell invasion assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpression of miR-126 inhibited GC cells invasion but did not affect its proliferation in vitro. |
target |
- |
- |
- |
CRMP1 |
protein-coding |
27864146 |
Cell proliferation assay; Cell invasion and migration assays; |
cell line |
- |
- |
- |
- |
- |
No Reports |
downregulation of CRMP1 increased cell proliferation and migration, and inhibited apoptosis in GC cells. Additionally, the inhibitory effect of the miR-187 inhibitor on cell migration was reversed by the downregulation of CRMP1. |
target |
- |
- |
- |
CRMP1 |
protein-coding |
27864146 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
CRMP1 was a direct downstream target of miR-187 in GC.The effects of miR-187 inhibitor on cell migration and cell apoptosis were reversed by CRMP1 downregulation |
target |
- |
- |
- |
CRNDE |
lncRNA |
28490034 |
qRT-PCR |
tissue |
China |
20 |
20 |
Up |
- |
No Reports |
CRNDE was highly expressed in GC cell lines and tissues; |
target |
- |
- |
- |
CRNDE |
lncRNA |
28490034 |
Cell proliferation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpression of CRNDE increased GC cell viability and promoted colony formation. Knockdown of CRNDE did not result in loss of expression-related effects on cell proliferation and colony formation. |
target |
- |
- |
- |
CRNDE |
lncRNA |
28490034 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-145 target gene E2F3 was strongly expressed following CRNDE competitive molecular sponging of miR-145. |
target |
- |
- |
- |
DNMT3A |
protein-coding |
26350239 |
Western blot |
tissue |
China |
35 |
35 |
Up |
- |
No Reports |
The average expression level of DNMT3A in the tumor tissues was signif_x005ficantly higher than that in the paired adjacent non-tumor tissues. DNMT3A overexpression was strongly correlated with tumor cell differentiation. |
target |
- |
- |
- |
DNMT3A |
protein-coding |
26350239 |
Cell proliferation assay; Flow Cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
DNMT3A promotes tumor cell proliferation and cell growth by disrupting the G1/S checkpoint. |
target |
- |
- |
- |
DNMT3A |
protein-coding |
26350239 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
DNMT3A promotes tumor cell proliferation in vivo |
target |
- |
- |
- |
DNMT3A |
protein-coding |
26350239 |
ChIP assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
DNMT3A modulated p18INK4C by directly binding to and silencing the p18INK4C gene via promoter hypermethylation. |
target |
- |
- |
- |
ERBB4 |
protein-coding |
29620274 |
Western blot |
tissue |
China |
27 |
27 |
Up |
- |
No Reports |
ERBB4 was highly expressed in gastric cancer tissues when compared to the normal stomach samples. |
target |
- |
- |
- |
ERBB4 |
protein-coding |
29620274 |
Cell proliferation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Silencing of ERBB4 expression suppresses GC cell proliferation. |
target |
- |
- |
- |
ERBB4 |
protein-coding |
29620274 |
Xenograft mouse models |
mice |
- |
- |
- |
- |
- |
No Reports |
Silencing of ERBB4 expression suppresses tumor growth in vivo. |
target |
- |
- |
- |
ERBB4 |
protein-coding |
29620274 |
IHC |
mice |
- |
- |
- |
- |
- |
No Reports |
inhibitor of ERBB4 (AST-1306) significantly downregulated the expression level of the prolif- eration-related proteins PI3K and Akt |
target |
- |
- |
- |
FADD |
protein-coding |
28848149 |
qRT-PCR |
tissue |
China |
34 |
34 |
Down |
- |
No Reports |
By further examining the underlying mechanism, we showed that H19/miR-675 axis inhibited expression of FADD. FADD downregulation subsequently inhibited the caspase cleavage cascades including caspase 8 and caspase 3. |
target |
- |
- |
- |
FADD |
protein-coding |
28848149 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
FADD is a potential target of miR-675; H19/miR-675 axis inhibited expression of FADD. FADD downregulation subsequently inhibited the caspase cleavage cascades including caspase 8 and caspase 3. |
target |
- |
- |
- |
FADD |
protein-coding |
28848149 |
Cell proliferation assay; Colony formation assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
FADD mediates the pro-proliferation and anti-apoptosis function of miR-675 |
target |
- |
- |
- |
FLJ22763 |
lncRNA |
30716442 |
qRT-PCR |
tissue |
China |
5 |
5 |
Down |
- |
No Reports |
FLJ22763, a novel lncRNA, had significantly lower expression in GC tissues. |
target/prognosis |
0.003 |
- |
- |
FLJ22763 |
lncRNA |
30716442 |
qRT-PCR |
tissue |
China |
303 |
- |
- |
Down |
No Reports |
Decreased expression of FLJ22763 was positively correlated with a lower-level histological grade and the depth of invasion. Patients with high FLJ22763 expression levels had a higher five-year survival rate. |
target/prognosis |
0.003 |
- |
- |
FLJ22763 |
lncRNA |
30716442 |
Cell proliferation assay; Invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
LncRNA FLJ22763 inhibits cells proliferation, migration, and invasion |
target/prognosis |
0.003 |
- |
- |
FLJ22763 |
lncRNA |
30716442 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
LncRNA FLJ22763 inhibits tumorigenesis of GC cells in vivo |
target/prognosis |
0.003 |
- |
- |
FLJ22763 |
lncRNA |
30716442 |
qRT-PCR; Cell tranfection; Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
FLJ22763 was negatively associated with ACLY, regulating the mRNA and protein levels of ACLY |
target/prognosis |
0.003 |
- |
- |
FZD7 |
protein-coding |
29559846 |
IHC |
tissue |
China |
251 |
60 |
Up |
- |
Not Related |
FZD7 was overexpressed in clinical GC samples, and thus was correlated with tumor invasion, lymphatic and organ metastasis, late TNM stages and poor patient survival. Furthermore, RNA interference-mediated . Moreover, ablation of FZD7 down-regulated EMT and the expression levels of cancer stem cell markers, and these inhibitions were associated with attenuated canonical Wnt/β-catenin signaling |
target/prognosis |
< 0.001 |
< 0.001 |
- |
FZD7 |
protein-coding |
29559846 |
Cell proliferation assay; Invasion and migration assays; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
Knockdown of FZD7 suppressed gastric cancer cell growth, migration and invasion |
target/prognosis |
< 0.001 |
< 0.001 |
- |
GAS5 |
lncRNA |
25959498 |
qRT-PCR |
tissue |
China |
55 |
55 |
Down |
- |
No Reports |
lncRNA GAS5 had lower expression in stomach cancer tissues than the normal counterparts. p21 expression correlates with lncRNA GAS5 expression in stomach cancer tissues. |
target |
- |
- |
- |
GAS5 |
lncRNA |
25959498 |
Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
lncRNA GAS5 knock-down abolishes cell cycle arrest at the G1 phase |
target |
- |
- |
- |
GAS5 |
lncRNA |
25959498 |
RNA pull-down assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
lncRNA GAS5 interacts with the transcriptional activator YBX1. |
target |
- |
- |
- |
GNAQ |
protein-coding |
28350126 |
IHC |
tissue |
China |
280 |
280 |
Up |
No |
No Reports |
GNAQ was highly expressed in GC patient samples and GNAQ expression was related to patient age, GC differentiation status and adjuvant therapy, as determined by immunohistochemical assay. Mechanistic analysis revealed that knockdown of GNAQ significantly increased the expression of p53 and p21, and decreased cyclin A and p-CDK2 protein expression. Moreover, the phosphorylation of ERK and MEK was also decreased after knockdown of GNAQ as determined by western blotting assay |
target |
- |
- |
- |
GNAQ |
protein-coding |
28350126 |
Cell proliferation assay; Cell colony formation assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
Silencing of GNAQ markedly suppressed proliferation and colony formation in GC cells, and arrested the cell cycle at the S phase. |
target |
- |
- |
- |
GNAQ |
protein-coding |
28350126 |
Western blot; cell transfection |
cell line |
- |
- |
- |
- |
- |
No Reports |
GNAQ directly or indirectly inhibits p53 and several key regulators of cell cycle signaling. GNAQ expression was required for MEK/ERK phosphorylation in MGC80-3 cells. |
target |
- |
- |
- |
hsa_circ_0000199 |
circRNA |
30927924 |
qRT-PCR |
tissue |
China |
149 |
0 |
- |
- |
No Reports |
The expression of circAKT3 was higher in CDDP-resistant GC tissues and cells than in CDDP-sensitive samples. It was an independent risk factor for disease-free survival. |
target/prognosis |
- |
0.0293 |
0.91 |
hsa_circ_0000199 |
circRNA |
30927924 |
Cell cytotoxicity assay; Clonogenic assay; Flow ytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
circAKT3 promotes DNA damage repair and inhibits the apoptosis of GC cells in vitro. Downregulation of circAKT3 facilitates cisplatin sensitivity of CDDP-resistant GC cells in vitro. |
target/prognosis |
- |
0.0293 |
0.91 |
hsa_circ_0000199 |
circRNA |
30927924 |
Luciferase reporter assay: RNA pull-down; FISH |
cell line |
- |
- |
- |
- |
- |
No Reports |
circAKT3 and miR-198 were colocalized in the cytoplasm; circAKT3 exerts its function by sponging miR-198. |
target/prognosis |
- |
0.0293 |
0.91 |
hsa_circ_0000199 |
circRNA |
30927924 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
circAKT3 promotes DNA damage repair and inhibits the apoptosis of GC cells in vivo. |
target/prognosis |
- |
0.0293 |
0.91 |
hsa_circ_0000993 |
circRNA |
30215537 |
qRT-PCR |
cell line |
- |
- |
- |
- |
- |
No Reports |
hsa_circ_0000993 has a lower expression level in highly aggressive cell line BGC-823 as compared with poorly aggressive cell line SGC-7901 |
target |
- |
- |
- |
hsa_circ_0000993 |
circRNA |
30215537 |
FISH |
cell line |
- |
- |
- |
- |
- |
No Reports |
FISH showed that hsa circ 0000993 was expressed both in nucleus and cytoplasm and mainly in nucleus of gastric cancer cells. |
target |
- |
- |
- |
hsa_circ_0000993 |
circRNA |
30215537 |
Cell proliferation assay; Invasion and migration assays; |
cell line |
- |
- |
- |
- |
- |
No Reports |
Increased expression of hsa circ 0000993 was associated with decreased migration, invasion and proliferation of gastric cancer cells. |
target |
- |
- |
- |
hsa_circ_0000993 |
circRNA |
30215537 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
hsa_circ_0000993 acts as a miRNA sponge for miR-214-5p |
target |
- |
- |
- |
hsa_circ_0092303 |
circRNA |
31182928 |
qRT-PCR |
tissue |
China |
30 |
30 |
Up |
- |
No Reports |
CircCACTIN expression was obviously up-regulated in GC tissues and cell lines. |
target |
- |
- |
- |
hsa_circ_0092303 |
circRNA |
31182928 |
Cell proliferation assay; Invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
CircCACTIN promotes proliferation, invasion, and migration of GC cells in vitro. |
target |
- |
- |
- |
hsa_circ_0092303 |
circRNA |
31182928 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
circCACTIN efficiently promoted GC tumor formation and EMT in vivo |
target |
- |
- |
- |
hsa_circ_0092303 |
circRNA |
31182928 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Binding interaction exists between circCACTIN and miR-331-3p. |
target |
- |
- |
- |
ITGA3 |
protein-coding |
23533596 |
IHC |
tissue |
China |
76 |
- |
- |
- |
No Reports |
The membranes of tumor cells stained positive for integrin a3. In all the tissues analyzed, high levels of integrin a3 expression were detected in 27 HGC tissue samples (35.52%).Patients with high integrin a3 expression were more likely to exhibit aggressive features. Patients with high Integrin a3 showed larger tumors (p =3.46E24), greater depth of invasion (p =0.001), higher tumor stage (p = 0.005), and more lymph node involvement (p = 0.040) than patients with low integrin a3 expression. Overexpression of Integrin a3 is Independent Factors Predicting the Prognosis of HGC Patients. |
target/prognosis |
< 0.0001 |
- |
- |
ITGA3 |
protein-coding |
23533596 |
Cell proliferation assay; Invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
silencing of integrin a3 markedly inhibited the invasion of HGC27 cells. |
target/prognosis |
< 0.0001 |
- |
- |
ITGA3 |
protein-coding |
23533596 |
Co-ip assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
CD151 formed a complex with integrin a3 in HGC cells. |
target/prognosis |
< 0.0001 |
- |
- |
KDM4B |
protein-coding |
24077348 |
Phase-contrast microscopy |
cell line |
- |
- |
- |
- |
- |
No Reports |
JMJD2B inhibition induces the epithelial morphology of gastric cancer cells |
target |
- |
- |
- |
KDM4B |
protein-coding |
24077348 |
qRT-PCR; Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
JMJD2B repression results in downregulation of mesenchymal markers and upregulation of epithelial markers |
target |
- |
- |
- |
KDM4B |
protein-coding |
24077348 |
Luciferase reporter activity assay; ChIP assay; |
cell line |
- |
- |
- |
- |
- |
No Reports |
JMJD2B is physically associated with b-catenin to regulate vimentin promoter. |
target |
- |
- |
- |
KDM4B |
protein-coding |
24077348 |
Cell invasion and migration assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
JMJD2B inhibition results in diminished invasion and metastasis in vitro |
target |
- |
- |
- |
KDM4B |
protein-coding |
24077348 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
JMJD2B knockdown inhibits tumor metastasis in vivo. |
target |
- |
- |
- |
KDM4B |
protein-coding |
24077348 |
IHC |
tissue |
China |
101 |
- |
- |
- |
No Reports |
JMJD2B expression was positively correlated with tumor size, differen_x005ftiation status, invasion, lymph node status, distant metastasis, and TNM stage of patients with gastric cancer |
target |
- |
- |
- |
KRT19P3 |
lncRNA |
31409899 |
qRT-PCR |
tissue |
China |
84 |
29 |
Down |
- |
No Reports |
KRT19P3 expression was significantly decreased in gastric cancer tissues. Lower expression of KRT19P3 was found to be associated with lager tumor size (≥ 5 cm), advanced TNM stage, Lauren's classification, and positive LNM. Patients with lower KRT19P3 expression had worse overall survival (OS) and disease-free sur_x005fvival (DFS) compared with those patients with higher KRT19P3 expression Univariate analysis demonstrated that patients with lower KRT19P3 expression tended to have a higher risk of death. |
target/prognosis |
0.0016 |
0.0028 |
- |
KRT19P3 |
lncRNA |
31409899 |
Cell proliferation assay; Cell invasion and migration assays; |
cell line |
- |
- |
- |
- |
- |
No Reports |
KRT19P3 inhibited GC cell proliferation and induced apoptosis, suppressed GC cell migration and invasion in vitro. |
target/prognosis |
0.0016 |
0.0028 |
- |
KRT19P3 |
lncRNA |
31409899 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
KRT19P3 suppressed GC cell migration and invasion and tumor growth in vivo. |
target/prognosis |
0.0016 |
0.0028 |
- |
KRT19P3 |
lncRNA |
31409899 |
RNA pull-down assay; RIP; Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
KRT19P3 could bind COPS7A directly and might regulate COPS7A activity in GC |
target/prognosis |
0.0016 |
0.0028 |
- |
LINC01089 |
lncRNA |
29717028 |
qRT-PCR |
tissue |
China |
32 |
32 |
Up |
- |
No Reports |
lncRNA AK096174 was up-regulated and associated with tumorigenesis, tumor size, metastasis, and poor prognosis in GC. Our data showed that AK096174 was highly expressed in the GC tissues and cell lines (SGC-7901, AGS, BGC-823, MGC-803), and patients with higher AK096174 expression had a poorer prognosis and shorter overall survival (OS). AK096174 knockdown inhibited the proliferation, migration, and invasiveness in SGC-7901 and BGC-823 cells, whereas AK096174 overexpression had the promoting effects. Furthermore, mechanistic investigation showed that AK096174 positively correlated with the expression of WD repeat-containing protein 66 (WDR66) gene at the translational level. Knockdown of WRD66 attenuated the positive impact of AK096174 in GC cells |
target |
- |
- |
- |
LINC01089 |
lncRNA |
29717028 |
Cell proliferation assay; Cell invasion and migration assays; |
cell line |
- |
- |
- |
- |
- |
No Reports |
AK096174 knockdown inhibited the proliferation, migration, and invasiveness in SGC-7901 and BGC-823 cells, whereas AK096174 overexpression had the promoting effects. |
target |
- |
- |
- |
LINC02859 |
lncRNA |
31207155 |
qRT-PCR |
tissue |
China |
90 |
90 |
Down |
- |
No Reports |
LOC101928316 was significantly downregulated in gastric cancer (GC) tissues specimen, GC cell lines, and associated with the GC patients tumor, node, and metastasis (TNM) stage and degree of differentiation. |
target |
- |
- |
- |
LINC02859 |
lncRNA |
31207155 |
Cell proliferation assay; Invasion and migration assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
LOC101928316 overexpression can significantly inhibit GC cell migration, invasion, and proliferation. |
target |
- |
- |
- |
LINC02859 |
lncRNA |
31207155 |
Xenograft mouse models |
mice |
- |
- |
- |
- |
- |
No Reports |
LOC101928316 Overexpression inhibited gastric cancer cells tumorigenesis in vivo |
target |
- |
- |
- |
LINC02859 |
lncRNA |
31207155 |
Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
lenti-LOC101928316-Overexpression stable infected can remarkably inhibit the expression level of PI3K, p-AKT, mTOR, and p-mTOR in GC cells |
target |
- |
- |
- |
MIR103A1 |
miRNA |
29754469 |
qRT-PCR |
tissue |
China |
33 |
33 |
|
- |
No Reports |
miR-103a-3p expression was regulated in GC tissues when compared with non-tissue samples, and was also upregulated in 18 poorly differentiated tumor tissues or in 24 tumor stage III/IV samples. |
target |
- |
- |
- |
MIR103A1 |
miRNA |
29754469 |
Cell proliferation assay; Cell colony formation assay;Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-103a-3p increases GC cell growth, and miR-103a-3p overexpression promotes the S-G2/M transition in vitro. |
target |
- |
- |
- |
MIR103A1 |
miRNA |
29754469 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-103a-3p directly regulates ATF7 expression in GC cells. |
target |
- |
- |
- |
MIR106B |
miRNA |
29434197 |
Luciferase reporter assay; Immunoblotting |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-106b-5p targets p21 to regulate the cellular senescence in BRD4-inhibited cells. BRD4 regulates miR-106b-5p transcription via E2F for cellular senescence. |
target |
- |
- |
- |
MIR107 |
miRNA |
26406411 |
qRT-PCR |
tissue |
Iran |
36 |
36 |
Up |
- |
|
Quantitative RT-PCR analysis on total RNA demonstrated significant overexpression of miR-107 in 36 GC tumor samples, in comparison to the its adjacent normal tissue of the same patients (p = 0.04) |
target |
- |
- |
- |
MIR126 |
miRNA |
25027343 |
qRT-PCR |
tissue |
China |
15 |
15 |
Down |
- |
No Reports |
MiR-126 expression was frequently and markedly downregulated (p < 0.05) in human gastric cancer tissues. Moreover, overexpression of miR-126 significantly decreased (p < 0.05) the protein levels of Crk, which has previously been identified as a direct target of miR-126. Knockdown of Crk also markedly suppressed GC cells invasion. |
target |
- |
- |
- |
MIR126 |
miRNA |
25027343 |
qRT-PCR |
tissue |
China |
110 |
- |
- |
- |
No Reports |
Low expression of miR-126 was significantly associated with lymph-node metastasis and poor histological grade. |
target |
- |
- |
- |
MIR126 |
miRNA |
25027343 |
Cell proliferation assay; Cell invasion assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpression of miR-126 inhibited GC cells invasion but did not affect its proliferation in vitro. |
target |
- |
- |
- |
MIR126 |
miRNA |
28260063 |
qRT-PCR |
cell line |
- |
- |
- |
- |
- |
No Reports |
the expression levels of miR-126 were significantly downregulated in the GC cell lines compared with the GES-1 cells |
target |
- |
- |
- |
MIR126 |
miRNA |
28260063 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
ADAM9 is a direct target post-transcriptionally regulated by miR-126 in GC cells. |
target |
- |
- |
- |
MIR1303 |
miRNA |
24647998 |
qRT-PCR |
tissue |
China |
45 |
45 |
Up |
Up |
No Reports |
miR-1303 was significantly overexpressed whereas claudin-18 was downregulated in GC tissues and cell lines, which was significantly associated with tumor size, location invasion, histologic type and tumor-node-metastasis stage. |
target |
- |
- |
- |
MIR1303 |
miRNA |
24647998 |
Cell proliferation assay; Cell invasion and migration assays; Cell colony formation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Cell proliferation rates were reduced, and cell invasion and migratory ability was significantly restricted in miR-1303 inhibitor-transfected groups. |
target |
- |
- |
- |
MIR1303 |
miRNA |
24647998 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-1303 could bind to the putative binding sites in CLDN18 mRNA 3'-UTR and visibly lower the expression of claudin-18. The introduction of claudin-18 without 3'-UTR restored the miR-1303 promoting migration function. |
target |
- |
- |
- |
MIR135B |
miRNA |
32119960 |
Luciferase reporter assay; RIP |
cell line |
- |
- |
- |
- |
- |
No Reports |
PCAT18 and CLDN11 are the direct targets of miR-135b |
target |
- |
- |
- |
MIR135B |
miRNA |
32119960 |
Cell proliferation assay; Cell invasion and migration assays; Cell colony forming assay; |
cell line |
- |
- |
- |
- |
- |
No Reports |
Over-expression of miR-135b promotes proliferation, migration and invasion of AGS cells via CLDN11 inhibition. |
target |
- |
- |
- |
MIR136 |
miRNA |
30468468 |
qRT-PCR |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-136 was significantly downregulated in the gastric cancer cell lines as compared to the normal cell line |
target |
- |
- |
- |
MIR136 |
miRNA |
30468468 |
Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
transfection of AGS cells with miR-136 promoted apoptosis |
target |
- |
- |
- |
MIR142 |
miRNA |
30178386 |
qRT-PCR |
tissue |
China |
101 |
101 |
Down |
- |
No Reports |
MiR-142-5p downregulation was significantly associated with the recurrence (P = 0.031) and poor prognosis of GC (P = 0.043). CYR61 was identified as a novel direct target of miR-142-5p by bioinformatics analysis of target prediction and luciferase reporter. The re-expression and knockdown of CYR61 could, respectively, rescue the effects induced by miR-142-5p overexpression and knockdown. MiR-142-5p attenuated GC cell migration and invasion, at least partially, by inactivation of the canonical Wnt/β-catenin signaling pathway through CYR61. |
target/prognosis |
0.001 |
- |
- |
MIR142 |
miRNA |
30178386 |
Cell invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
MiR-142-5p inhibited cancer cell migration and invasion both in vitro and in vivo. |
target/prognosis |
0.001 |
- |
- |
MIR142 |
miRNA |
30178386 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
MiR-142-5p inhibited cancer cell migration and invasion in vivo. |
target/prognosis |
0.001 |
- |
- |
MIR142 |
miRNA |
30178386 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
CYR61 is a novel target of miR‑142‑5p in GC cells |
target/prognosis |
0.001 |
- |
- |
MIR143 |
miRNA |
28404925 |
microarray chip; qRT-PCR |
tissue |
China |
42 |
42 |
Down |
Down |
Related |
miR-143-3p was ignificantly increased miRNA in H. pylori-positive gastric cancer tissues and was significantly decreased in gastric cancer tissues and cells, which correlated with late stage and lymph node metastasis. |
target |
- |
- |
- |
MIR143 |
miRNA |
28404925 |
Cell proliferation assay; Invasion and migration assays; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpression of miR-143-3p suppressed cell proliferation, induced apoptosis and inhibited cell migration and invasion. |
target |
- |
- |
- |
MIR143 |
miRNA |
28404925 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
AKT2 is a direct target of miR-143-3p |
target |
- |
- |
- |
MIR148A |
miRNA |
27518872 |
qRT-PCR |
tissue |
China |
41 |
41 |
Down |
- |
No Reports |
miR-148a expression was significantly down-regulated in gastric cancer tissues in comparison with the matched normal mucosal tissues, and its expression was statistically associated with lymph node metastasis. |
target |
- |
- |
- |
MIR148A |
miRNA |
27518872 |
Cell proliferation assay; Cell migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
Ectopic expression of miR-148a inhibited tumor cell proliferation and migration in vitro. More importantly, siRNA-induced knockdown of CCK-BR elicited similar anti-oncogenic effects (decreased proliferation and migration) as those induced by enforced miR-148a expression. |
target |
- |
- |
- |
MIR148A |
miRNA |
27518872 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
Ectopic expression of miR-148a inhibited tumor formation in vivo. |
target |
- |
- |
- |
MIR148A |
miRNA |
27518872 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Cholecystokinin B receptor (CCK-BR) was a direct target of miR-148a |
target |
- |
- |
- |
MIR152 |
miRNA |
28427226 |
qRT-PCR |
tissue |
China |
42 |
42 |
Down |
- |
No Reports |
The expression of miR-152 in human gastric cancer tissues were significantly lower than that in matched adjacent normal tissues. Meanwhile, lower miR-152 was also found in gastric cancer cell lines. The stage, tumor size and lymph node metastasis rate were significant higher in low-miR-152 group in clinical patients. |
target |
- |
- |
- |
MIR152 |
miRNA |
28427226 |
Cell proliferation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Elevation of miR-152 enhanced T cells proliferation and effector cytokines production via inhibiting B7-H1/PD-1 pathway. |
target |
- |
- |
- |
MIR152 |
miRNA |
28427226 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-152 directly bind to B7-H1 3' untranslated region in gastric cancer cell and inhibited B7-H1 expression. |
target |
- |
- |
- |
MIR155 |
miRNA |
26955820 |
qRT-PCR |
tissue |
China |
60 |
60 |
Down |
Down |
No Reports |
miR-155 levels were significantly lower in both GC tissues and GC cell lines than in their normal controls, and its expression inversely correlated with tumor size and the pathologic stage. |
target |
- |
- |
- |
MIR155 |
miRNA |
26955820 |
Cell proliferation assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
Enforced expression of miR-155 impaired GC cell proliferation, promoted G1 phase arrest and induced apoptosis in vitro. In addition, we identified cyclin D1 as the direct target of miR-155, and knockdown of cyclin D1 partially phenocopied the role of miR-155 in GC cells. |
target |
- |
- |
- |
MIR155 |
miRNA |
26955820 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Cyclin D1 is a direct target of miR‐155 in GC cells |
target |
- |
- |
- |
MIR17 |
miRNA |
20234369 |
qRT-PCR |
plasma |
Japan |
69 |
30 |
Up |
- |
|
miR-17-5p were significantly higher in GC patients than in controls (P = 0.006) |
target |
- |
- |
- |
MIR187 |
miRNA |
27864146 |
qRT-PCR |
tissue |
China |
54 |
54 |
Up |
- |
No Reports |
miR-187 was significantly overexpressed in GC tissues compared to that in non-tumor tissues and was associated with malignant clinical factors such as depth of invasion (P = 0.005), tumor size (P = 0.024), lymph node metastasis (P = 0.048), and TNM stage (P = 0.035). |
target |
- |
- |
- |
MIR187 |
miRNA |
27864146 |
Cell proliferation assay; Cell invasion and migration assays; |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-187 significantly increased migration, invasion, and proliferation, but inhibited apoptosis in GC cells |
target |
- |
- |
- |
MIR187 |
miRNA |
27864146 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
miR-187 promoted tumor growth in vivo |
target |
- |
- |
- |
MIR187 |
miRNA |
27864146 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
CRMP1 was a direct downstream target of miR-187 in GC.The effects of miR-187 inhibitor on cell migration and cell apoptosis were reversed by CRMP1 downregulation |
target |
- |
- |
- |
MIR191 |
miRNA |
24603541 |
qRT-PCR |
tissue |
China |
75 |
75 |
Up |
Up |
|
The miR-191 Cluster Is Highly Expressed in Gastric Cancer (GC) |
target |
- |
- |
- |
MIR191 |
miRNA |
24603541 |
qRT-PCR |
serum |
China |
57 |
58 |
Up |
Up |
|
when using miR-16 as an endogenous control, the relative level of miR-191 in GC serum was significantly higher than those in the controls (p < 0.01) |
target,diagnosis |
- |
- |
0.85 |
MIR194-1 |
miRNA |
27810403 |
qRT-PCR |
tissue |
China |
43 |
43 |
Up |
- |
No Reports |
MiRNA-194 was found to be overexpressed in GC cell lines and 43 paired GC tissues. |
target |
- |
- |
- |
MIR194-1 |
miRNA |
27810403 |
Cell proliferation assay; Cell invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpression of miRNA-194 promoted cell proliferation and migration, while inhibition of miRNA-194 blocked these processes. |
target |
- |
- |
- |
MIR194-1 |
miRNA |
27810403 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
Inhibition of miRNA-194 decreased tumor volumes in nude mice. |
target |
- |
- |
- |
MIR194-1 |
miRNA |
27810403 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
SUFU is the functional target of miRNA-194 |
target |
- |
- |
- |
MIR199A1 |
miRNA |
30193607 |
qRT-PCR |
tissue |
China |
51 |
51 |
Down |
- |
No Reports |
The relative expression of miR-199 in gastric carcinoma tissues was significantly lower than that in the adjacent normal tissue . |
target |
- |
- |
- |
MIR199A1 |
miRNA |
30193607 |
Cell proliferation assay; Cell migration assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Over-expression of miR-199 inhibited the proliferation and migration of GC cells. |
target |
- |
- |
- |
MIR199A1 |
miRNA |
30193607 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-199 directly targeted on the 3' untranslated region of TBL1XR1. |
target |
- |
- |
- |
MIR19A |
miRNA |
25914465 |
qRT-PCR |
tissue |
China |
50 |
50 |
Up |
Up |
No Reports |
miR19a is increased in GC tissue samples and cell lines. Overexpression of miR-19a was significantly associated with metastasis of GC. |
target |
- |
- |
- |
MIR19A |
miRNA |
25914465 |
Cell proliferation assay; Invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpression of miR-19a promoted the proliferation, migration and invasion. |
target |
- |
- |
- |
MIR19A |
miRNA |
25914465 |
Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpressing miR19a GC cells promoted phosphorylation of PI3KAKT, and the phosphorylation of PI3KAKT was blocked in the cells transfected with miR-19a mimic. |
target |
- |
- |
- |
MIR203A |
miRNA |
30837034 |
qRT-PCR |
tissue |
China |
10 |
10 |
Down |
- |
No Reports |
miR-203 is downregulated in GC tissues and cell lines. Moreover, the low level of miR-203 was associated with increased expression of annexin A4 in GC tissues and cell lines. |
target |
- |
- |
- |
MIR203A |
miRNA |
30837034 |
Cell invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-203 Suppressed the Invasion and EMT of GC Cells Through Inhibition of Annexin A4 |
target |
- |
- |
- |
MIR203A |
miRNA |
30837034 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-203 Directly Targets Annexin A4 in GC Cells |
target |
- |
- |
- |
MIR203A |
miRNA |
30837034 |
qRT-PCR; Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
overexpression of miR-203 could inhibit EMT of GC cells |
target |
- |
- |
- |
MIR208A |
miRNA |
29886152 |
qRT-PCR |
tissue |
China |
62 |
62 |
Up |
Up |
No Reports |
miR-208a expression was significantly increased in GC tissues compared with adjacent normal tissues. Higher miR-208a expression was association with lymph node metastasis and TNM stage in GC patients. Kaplan-Meier analysis verified that patients with higher miR-208a expression were significantly associated with shorter overall survival (OS) time. miR-208a expression negatively associated with MEG3. |
target/prognosis |
< 0.05 |
- |
- |
MIR208A |
miRNA |
29886152 |
Cell proliferation assay; Cell invasion assay; |
cell line |
- |
- |
- |
- |
- |
No Reports |
Ectopic expression of miR-208a by treatment with miR-208a mimic promoted cell proliferation and invasion abilities, but downregulation of miR-208a by treatment with miR-208a inhibitor had an opposite effects. |
target/prognosis |
< 0.05 |
- |
- |
MIR208A |
miRNA |
29886152 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
SFRP1 is a direct target of MiR-208a in GC cells |
target/prognosis |
< 0.05 |
- |
- |
MIR208A |
miRNA |
29886152 |
Luciferase reporter assay; RIP |
cell line |
- |
- |
- |
- |
- |
No Reports |
MEG3 is a bona fide target for miR-208a in GC cells |
target/prognosis |
< 0.05 |
- |
- |
MIR208A |
miRNA |
27634902 |
qRT-PCR |
tissue |
China |
16 |
16 |
Up |
- |
No Reports |
miR-208a-3p was up-regulated in GC tissues |
target |
- |
- |
- |
MIR208A |
miRNA |
27634902 |
Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-208a-3p suppresses apoptosis of gastric cancer cells by targeting PDCD4 |
target |
- |
- |
- |
MIR208A |
miRNA |
27634902 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
PDCD4 is a direct target of miR-208a-3p |
target |
- |
- |
- |
MIR208A |
miRNA |
27634902 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
miR-208a-3p promoted the development of tumor growth |
target |
- |
- |
- |
MIR21 |
miRNA |
30700111 |
Cell proliferation assay; Migration assay; Flow cytometer; Cell cycle assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Down-regulation of miR-21 markedly reduced gastric cancer cell proliferation and promoted cell apoptosis and repressed cell cycle progression; Silencing miR-21 dramatically blocked gastric cancer cell migration and movement. |
target |
- |
- |
- |
MIR222 |
miRNA |
22432036 |
qRT-PCR |
serum |
- |
82 |
82 |
UP |
- |
|
miR-222 demonstrated significantly elevated levels in GC group with more than 2-fold change(P<0.05) |
target |
- |
- |
0.65 |
MIR222 |
miRNA |
25129310 |
qRT-PCR |
plasma |
China |
114 |
56 |
UP |
- |
|
In this study, our results demonstrated that the levels of circulating miR-222 in patients with GC were significantly increased, compared with CAG and healthy controls. In addition, higher level of circulating miR-222 had also been found in the plasma of CAG patients compared with healthy controls, indicating the dysregulated expression of miR-222 might be involved in the early events of GC malignancy. |
target;prognosis |
22.428 % |
25.267% |
0.85 |
MIR27A |
miRNA |
27409164 |
qRT-PCR |
tissue |
China |
20 |
20 |
Up |
- |
No Reports |
Two isoforms of mature miR-27a, miR-27a-5p and miR-27-3p, were both frequently overexpressed in gastric cancer tissues and cell lines, whereas the expression level of miR-27-3p in gastric cancer was significantly higher than that of miR-27a-5p. |
target |
- |
- |
- |
MIR27A |
miRNA |
27409164 |
Cell proliferation assay; Invasion and migration assays; Flow cytometry; Apotosis assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpression of miR-27a-3p, but not miR-27a-5p, markedly promoted gastric cancer cell proliferation in vitro. miR-27a-3p/BTG2 axis regulates cell cycle progression and apoptosis in gastric cancer cells |
target |
- |
- |
- |
MIR27A |
miRNA |
27409164 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
miR-27a-3p promotes GC cell growth in vivo. |
target |
- |
- |
- |
MIR27A |
miRNA |
27409164 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
BTG2 was a direct and functional target of miR-27a-3p in gastric cancer and miR-27a-3p inhibition obviously up-regulated the expression of BTG2. |
target |
- |
- |
- |
MIR29A |
miRNA |
25428377 |
qRT-PCR |
tissue |
China |
20 |
20 |
Down |
- |
No Reports |
Down-regulated in GC tissues compared with non-tumor tissues and had the tendency of inversely relationship with the expression of AKT2. |
target |
- |
- |
- |
MIR29A |
miRNA |
25428377 |
Cell invasion assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Introduction of miR-29a into GC cells resulted in decreased AKT2 expression and decreased the ability of cancer cells invasion, so did the siRNA-AKT2. |
target |
- |
- |
- |
MIR29A |
miRNA |
25428377 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
AKT2 was the direct target of the miR-29a in GC cells. |
target |
- |
- |
- |
MIR29B1 |
miRNA |
25428377 |
qRT-PCR |
tissue |
China |
20 |
20 |
Down |
- |
No Reports |
Down-regulated in GC tissues compared with non-tumor tissues and had the tendency of inversely relationship with the expression of AKT2. |
target |
- |
- |
- |
MIR29B1 |
miRNA |
25428377 |
Cell invasion assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Introduction of miR-29b into GC cells resulted in decreased AKT2 expression and decreased the ability of cancer cells invasion, so did the siRNA-AKT2. |
target |
- |
- |
- |
MIR29B1 |
miRNA |
25428377 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
AKT2 was the direct target of the miR-29b in GC cells. |
target |
- |
- |
- |
MIR29C |
miRNA |
25428377 |
qRT-PCR |
tissue |
China |
20 |
20 |
Down |
- |
No Reports |
Down-regulated in GC tissues compared with non-tumor tissues and had the tendency of inversely relationship with the expression of AKT2. |
target |
- |
- |
- |
MIR29C |
miRNA |
25428377 |
Cell invasion assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Introduction of miR-29c into GC cells resulted in decreased AKT2 expression and decreased the ability of cancer cells invasion, so did the siRNA-AKT2. |
target |
- |
- |
- |
MIR29C |
miRNA |
25428377 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
AKT2 was the direct target of the miR-29c in GC cells. |
target |
- |
- |
- |
MIR320A |
miRNA |
29152656 |
qRT-PCR |
tissue |
China |
40 |
40 |
Down |
- |
No Reports |
Downregulated in GC tumor tissues; miR‑320a is negatively correlated with ADAM10 in tumors |
target |
- |
- |
- |
MIR320A |
miRNA |
29152656 |
Colony formation assay; MTS assay; Viability assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR‑320a inhibits cell growth and enhances sensitivity of GC cells to cisplatin and suppresses tumor growth in vivo. |
target |
- |
- |
- |
MIR320A |
miRNA |
29152656 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR‑320a directly targets ADAM10 in GC cells. |
target |
- |
- |
- |
MIR331 |
miRNA |
31182928 |
Cell proliferation assay; Invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
Transfection of miR-331-3p inhi- bitor promoted BGC-823 cells proliferation, invasion and migration; transfection of miR-331-3p mimic suppressed MGC-803 cells proliferation, invasion and migration. |
target |
- |
- |
- |
MIR331 |
miRNA |
31182928 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Binding interaction exists between miR-331-3p and TGFBR1, circCACTIN and miR-331-3p |
target |
- |
- |
- |
MIR331 |
miRNA |
31182928 |
qRT-PCR; Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
Both TGFBR1 mRNA and protein expression were regulated by circCACTIN through miR-331-3p |
target |
- |
- |
- |
MIR335 |
miRNA |
21822301 |
qRT-PCR |
tissue |
China |
70 |
70 |
No |
Down |
No Reports |
Low expression of miR-335 was significantly associated with lymph-node metastasis, poor pT stage, poor pN stage and invasion of lymphatic vessels. Patients with a better pT stage or pN stage had significantly higher miR-335 expression. Patients with a low expression of miR-335 tended to have metastasis invasion into lymphatic vessels. |
target |
- |
- |
- |
MIR335 |
miRNA |
21822301 |
Cell invasion assay; Tumor metastasis formation assay; MTT proliferation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-335 suppresses gastric cancer invasion and metastasis in vitro, but has no significant effects on cell proliferation of gastric cancer |
target |
- |
- |
- |
MIR335 |
miRNA |
21822301 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
SP1 and Bcl-w are direct targets of miR-335. miR-335 suppresses gastric cancer invasion and metastasis by targeting Bcl-w and SP1 |
target |
- |
- |
- |
MIR338 |
miRNA |
30308487 |
qRT-PCR |
tissue |
China |
53 |
53 |
Down |
- |
No Reports |
miR-338-3p was down-regulated in both GC tissues (53 paired samples) and cell lines (4 cancer cell lines). The decreased expression of miR-338-3p was found to be significantly associated with the Borrmann stage. |
target |
- |
- |
- |
MIR338 |
miRNA |
30308487 |
Cell proliferation assay; Invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-338-3p could suppress cell proliferation and induce cell apoptosis, suppresses metastasis |
target |
- |
- |
- |
MIR338 |
miRNA |
30308487 |
Bisulfite sequence |
cell line |
- |
- |
- |
- |
- |
No Reports |
hyper-methylation is the main cause of miR-338-3p depression |
target |
- |
- |
- |
MIR338 |
miRNA |
30308487 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Rab14 is a direct target of miR-338-3p; miR-338-3p suppresses metastasis by targeting the Hhat-MMP signaling pathway |
target |
- |
- |
- |
MIR338 |
miRNA |
26617808 |
qRT-PCR |
tissue |
China |
36 |
36 |
Down |
- |
No Reports |
Down-regulated in both gastric cancer cell lines and tissues. |
target |
- |
- |
- |
MIR338 |
miRNA |
26617808 |
Cell proliferation assay; Invasion and migration assays; |
cell line |
- |
- |
- |
- |
- |
No Reports |
Enforced expression of miR-338-3p inhibited proliferation, migration and invasion of gastric cancer cells in vitro |
target |
- |
- |
- |
MIR338 |
miRNA |
26617808 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
ADAM17 is a direct target of miR-338-3 and prescued the miR-338-3p mediated inhibition of cell proliferation, migration and invasion |
target |
- |
- |
- |
MIR338 |
miRNA |
25945841 |
qRT-PCR |
tissue |
China |
20 |
20 |
Down |
Down |
No Reports |
miR-338-3p was significantly lower in GC tissues than in the corresponding adjacent noncancerous tissues; mRNA expression of miR-338-3p was even lower in advanced stages of GC compared to that observed in the early stages. |
target |
- |
- |
- |
MIR338 |
miRNA |
25945841 |
Cell invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-338-3p inhibited the migration and invasion of GC cells in vitro and inhibits the EMT process in GC cells. |
target |
- |
- |
- |
MIR338 |
miRNA |
25945841 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-338-3p directly targeted zinc finger E-box-binding protein 2 (ZEB2) and metastasis-associated in colon cancer-1 (MACC1). |
target |
- |
- |
- |
MIR340 |
miRNA |
28057912 |
Cell proliferation assay; Invasion and migration assays; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpression of miR-340 significantly reduced cell viability and proliferation, and induced cell apoptosis of GC cells |
target |
- |
- |
- |
MIR381 |
miRNA |
28193228 |
qRT-PCR |
tissue |
China |
103 |
103 |
Down |
- |
No Reports |
MiR-381 was significantly down-regulated in gastric cancer tissues and cell lines. Low expression of miR-381 was negatively related to lymph node metastasis, advanced tumor stage and poor prognosis.miR-381 and TMEM16A revealed the improved prognostic accuracy for gastric cancer patients. |
target/prognosis |
0.024 |
0.037 |
- |
MIR381 |
miRNA |
28193228 |
Cell proliferation assay; Invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
MiR-381 decreased gastric cancer cell proliferation, migration and invasion in vitro. |
target/prognosis |
0.024 |
0.037 |
- |
MIR381 |
miRNA |
28193228 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
MiR-381 decreased gastric cancer cell proliferation, migration and invasion in vivo. |
target/prognosis |
0.024 |
0.037 |
- |
MIR381 |
miRNA |
28193228 |
Luciferase reporter assay; Western blot; IHC |
cell line |
- |
- |
- |
- |
- |
No Reports |
TMEM16A was identified as a direct target of miR-381 and the expression of miR-381 was inversely correlated with TMEM16A expression in gastric cancer tissues |
target/prognosis |
0.024 |
0.037 |
- |
MIR519D |
miRNA |
29510377 |
qRT-PCR |
tissue |
China |
20 |
20 |
Down |
|
No Reports |
miR-519d-3p was downregulated in GC tumor tissues,associated with the clinical stage and lymph node metastasis of GC tissues. Decreased miR-519d-3p expression was associated with advanced stage and lymph node metastasis of GC compared with controls. |
target |
- |
- |
- |
MIR519D |
miRNA |
29510377 |
Cell proliferation assay; Invasion and migration assays; Cell colony formation assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-519d-3p inhibited MGC803 cell proliferation and invasion and delayed G1/S phase transition.miR-519d-3p/BCL6 axis inhibits cell proliferation, invasion, and cell cycle by regulating cyclin B1, E-cadherin, and MMP2 levels in GC cells. |
target |
- |
- |
- |
MIR519D |
miRNA |
29510377 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
BCL6 Is the Target of miR-519d-3p |
target |
- |
- |
- |
MIR519D |
miRNA |
29510377 |
qRT-PCR |
tissue |
China |
20 |
20 |
Down |
|
No Reports |
miR-519d-3p was downregulated in GC tumor tissues,associated with the clinical stage and lymph node metastasis of GC tissues. Decreased miR-519d-3p expression was associated with advanced stage and lymph node metastasis of GC compared with controls. |
target |
- |
- |
- |
MIR5590 |
miRNA |
30029874 |
qRT-PCR |
tissue |
China |
42 |
42 |
Down |
- |
No Reports |
In addition, Ago2-based RIP and dual-luciferase reporter were conducted to study the Next, were used to determine the role of miR-5590-3p in GC tumorigenicity in vivo. whereas . |
target |
- |
- |
- |
MIR5590 |
miRNA |
30029874 |
Cell proliferation assay; Cell colony formation assay; |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-5590-3p regulates GC cell proliferation and colony formation by G1/S transition |
target |
- |
- |
- |
MIR5590 |
miRNA |
30029874 |
Xenograft mouse models |
mice |
- |
- |
- |
- |
- |
No Reports |
Downregulation of miR-5590-3p promoted GC proliferation in vitro |
target |
- |
- |
- |
MIR5590 |
miRNA |
30029874 |
RIP and Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-5590-3p as a direct target of DDX5. |
target |
- |
- |
- |
MIR582 |
miRNA |
29228422 |
qRT-PCR |
tissue |
China |
42 |
42 |
|
|
No Reports |
MiR-582-5p was downregulated in gastric cancer tissues when compared with para-carcinoma tissues. |
target |
- |
- |
- |
MIR582 |
miRNA |
29228422 |
Cell proliferation assay; Cell colony formation assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpressed miR-582-5p could attenuate cell proliferation and viability capacities, as well as promoted cell apoptosis and cell cycle arrest at G0/G1 phase. |
target |
- |
- |
- |
MIR582 |
miRNA |
29228422 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
AKT3 was chosen as the target gene of miR-582-5p. Moreover, restoration of AKT3 could impair tumor suppression role of miR-582-5p on gastric cancer growth. |
target |
- |
- |
- |
MIR589 |
miRNA |
30012200 |
qRT-PCR |
tissue |
China |
34 |
34 |
Up |
- |
No Reports |
MiR-589 expression was significantly higher in tumor tissues and gastric cancer cells than those in matched normal tissues and gastric epithelial cells, respectively. Overexpression of miR-589 is associated with tumor metastasis, invasion and poor prognosis of GC patients. |
target |
- |
- |
- |
MIR589 |
miRNA |
30012200 |
Cell invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
Gain- and loss-of function experiments showed that miR-589 promoted cell migration, metastasis and invasion in vitro and lung metastasis in vivo. |
target |
- |
- |
- |
MIR589 |
miRNA |
30012200 |
nude mouse xenograft model |
mice |
- |
- |
- |
- |
- |
No Reports |
Endogenous overexpression of miR-589 promotes metastasis of GC cell in vivo |
target |
- |
- |
- |
MIR589 |
miRNA |
30012200 |
Luciferase reporter assay; ChIP assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-589 directly targeted LIFR to activate PI3K/AKT/c-Jun signaling. c-Jun bound to the promoter region of miR-589 and activated its transcription. |
target |
- |
- |
- |
MIR613 |
miRNA |
28701053 |
qRT-PCR |
tissue |
China |
52 |
52 |
Down |
- |
No Reports |
miR-613 was evidently downregulated in gastric cancer tissue and cell. |
target |
- |
- |
- |
MIR613 |
miRNA |
28701053 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
CDK9 is a direct target of miR-613 in gastric cancer |
target |
- |
- |
- |
MIR613 |
miRNA |
28701053 |
Cell proliferation assay; Invasion and migration assays; |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-613 suppressed cell proliferation and migration in gastric cancer |
target |
- |
- |
- |
MIR644A |
miRNA |
27983935 |
qRT-PCR |
tissue |
China |
107 |
107 |
Down |
Down |
No Reports |
The expression of miR-644a was suppressed in GC tissues and was associated with a later clinical stage and tumor metastasis. |
target |
- |
- |
- |
MIR644A |
miRNA |
27983935 |
Cell proliferation assay; Cell invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
Restoring the expression of miR-644a could significantly suppress the migration and invasion of HGC-27 and SGC-7901 cells, which might be correlated to its suppressive effect on the EMT process. |
target |
- |
- |
- |
MIR644A |
miRNA |
27983935 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
CtBP1 is a putative target gene of miR-644a in GC cells |
target |
- |
- |
- |
MIR675 |
miRNA |
28848149 |
qRT-PCR;Western blot |
tissue |
China |
34 |
34 |
Up |
- |
No Reports |
miR-675 were increased in gastric cancer cell lines and tissues. H19 and miR-675 expression was positively correlated in gastric cancer tissues. |
target |
- |
- |
- |
MIR675 |
miRNA |
28848149 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
FADD is a potential target of miR-675; H19/miR-675 axis inhibited expression of FADD. FADD downregulation subsequently inhibited the caspase cleavage cascades including caspase 8 and caspase 3. |
target |
- |
- |
- |
MIR675 |
miRNA |
28848149 |
Cell proliferation assay; Colony formation assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpression of H19 and miR-675 promoted cell proliferation and inhibited cell apoptosis, whereas knockdown of H19 and miR-675 inhibited these effects. |
target |
- |
- |
- |
MIR675 |
miRNA |
28848149 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
There was a dramatic decrease in in tumor volume and weight in nude mice in which LV- shH19 infected SGC-7901 cell. co-infection with LV-miR675 partially reversed this tendency. |
target |
- |
- |
- |
MIR711 |
miRNA |
26735582 |
qRT-PCR |
tissue |
China |
28 |
28 |
Down |
- |
No Reports |
The expression of miR-711 was lower in the cancer tissues than in the normal tissues. |
target |
- |
- |
- |
MIR711 |
miRNA |
26735582 |
Cell proliferation assay; Invasion and migration assays; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-711 could suppress SGC-7901 cell growth in a time-dependent manner. |
target |
- |
- |
- |
MIR711 |
miRNA |
26735582 |
Flow cytometry; Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
miR-711 was found to downregulate CDK4 expression |
target |
- |
- |
- |
MIRLET7B |
miRNA |
30237418 |
qRT-PCR |
cell line |
- |
- |
- |
- |
- |
No Reports |
let-7b-expression level of SGC7901/DDP cells was significantly lower than for its parental SGC7901 cells. |
target |
- |
- |
- |
MIRLET7B |
miRNA |
30237418 |
Cell proliferation assay; Flow cytometry; |
cell line |
- |
- |
- |
- |
- |
No Reports |
Upregulation of let-7b could reverse the DDP resistance of gastric cancer SGC7901/DDP cells by inducing cell viability inhibition and apoptosis when exposed to DDP treatment. |
target |
- |
- |
- |
MIRLET7B |
miRNA |
30237418 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
let-7b directly targets AURKB by binding to its 3'UTR region in DDP-resistant gastric cancer cells to DDP. |
target |
- |
- |
- |
MIRLET7B |
miRNA |
30237418 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
Upregulation of let-7b inhibited tumor growth derived from DDP-resistant cells in vivo. |
target |
- |
- |
- |
MIRLET7B |
miRNA |
25288334 |
qRT-PCR |
tissue |
China |
76 |
76 |
Down |
- |
No Reports |
let-7b was down-regulated in gastric cancer and its downregulation was associated with poor survival and correlated with lymph node metastasis. AKT2 mRNA expression showed negative correlation with the expression of let-7b in primary tumors. |
target/prognosis |
- |
0.001 |
- |
MIRLET7B |
miRNA |
25288334 |
Cell proliferation assay; Invasion assay; Cell colony fomation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
suppressed the growth and invasive capacityof GC cells |
target/prognosis |
- |
0.001 |
- |
MIRLET7B |
miRNA |
25288334 |
Xenograft mouse models |
mice |
- |
- |
- |
- |
- |
No Reports |
let-7b/g transfectants formed smaller xenografts than those scramble transfectants |
target/prognosis |
- |
0.001 |
- |
MIRLET7B |
miRNA |
25288334 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
let-7b/g inhibited AKT2 expression by directly binding to its 3'UTR, reduced p-AKT (S473) activation and suppressed expression of the downstream effector pS6. |
target/prognosis |
- |
0.001 |
- |
MIRLET7B |
miRNA |
25510669 |
qRT-PCR |
tissue |
China |
47 |
47 |
Down |
- |
Related |
Let-7b was found downregulated remarkably in gastric cancer tissues and was correlated with Helicobacter pylori infection, tumor stage, and lymphatic metastasis. |
target |
- |
- |
- |
MIRLET7B |
miRNA |
25510669 |
Cell proliferation assay; Cell invasion and migration assays; Cell colony formation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Ectopic expression of let-7b suppressed the growth, migration, invasion, and tumorigenicity of GC cells, whereas let-7b knockdown promoted these phenotypes. |
target |
- |
- |
- |
MIRLET7B |
miRNA |
25510669 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
Let-7b suppresses the tumorigenicity in vivo. |
target |
- |
- |
- |
MIRLET7B |
miRNA |
25510669 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Cthrc1 was a direct target of let-7b. |
target |
- |
- |
- |
MIRLET7G |
miRNA |
25288334 |
qRT-PCR |
tissue |
China |
76 |
76 |
Down |
- |
No Reports |
let-7g was found down-regulated in gastric cancer and correlated with N-stage and lymph node metastasis. AKT2 mRNA expression showed negative correlation with the expression of let-7g in primary tumors. |
target |
- |
0.051 |
- |
MIRLET7G |
miRNA |
25288334 |
Cell proliferation assay; Invasion assay; Cell colony fomation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
suppressed the growth and invasive capacityof GC cells |
target |
- |
0.051 |
- |
MIRLET7G |
miRNA |
25288334 |
Xenograft mouse models |
mice |
- |
- |
- |
- |
- |
No Reports |
let-7b/g transfectants formed smaller xenografts than those scramble transfectants |
target |
- |
0.051 |
- |
MIRLET7G |
miRNA |
25288334 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
let-7b/g inhibited AKT2 expression by directly binding to its 3'UTR, reduced p-AKT (S473) activation and suppressed expression of the downstream effector pS6. |
target |
- |
0.051 |
- |
NOTCH4 |
protein-coding |
25511451 |
IHC |
tissue |
China |
75 |
75 |
Up |
- |
No Reports |
Notch4 was activated by overexpressing exogenous intracellular domain of Notch4 (ICN4). Activated Notch4 expression levels were up-regulated in GC tissues |
target |
- |
- |
- |
NOTCH4 |
protein-coding |
25511451 |
Cell proliferation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Notch4 activation promoted GC growth in vitro, while Notch4 inhibition using ICN4 siRNA had opposite effects. |
target |
- |
- |
- |
NOTCH4 |
protein-coding |
25511451 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
Notch4 activation promotes tumor growth in vivo, while Notch4 inhibition inhibits tumor growth in vivo |
target |
- |
- |
- |
PCAT18 |
lncRNA |
32119960 |
Cell proliferation assay; Cell invasion and migration assays; Cell colony forming assay; |
cell line |
- |
- |
- |
- |
- |
No Reports |
PCAT18 down-expression promoted proliferation, migration and invasion of gastric cancer cells. |
target |
- |
- |
- |
PCAT18 |
lncRNA |
32119960 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
In in-vivo experiment, PCAT18 over-expression restrained tumor growth and metastasis. |
target |
- |
- |
- |
PCAT18 |
lncRNA |
32119960 |
Luciferase reporter assay; RIP |
cell line |
- |
- |
- |
- |
- |
No Reports |
PCAT18 is the direct target of miR-135b |
target |
- |
- |
- |
PDCD4 |
protein-coding |
27634902 |
IHC |
tissue |
China |
16 |
16 |
Down |
- |
No Reports |
PDCD4 protein expression is down-regulated in GC tissues. |
target |
- |
- |
- |
PDCD4 |
protein-coding |
27634902 |
Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
MKN45 cells transfected with the PDCD4 siRNA showed suppression of cell apoptosis, whereas overexpression of PDCD4 significantly promoted cell apoptosis |
target |
- |
- |
- |
PDCD4 |
protein-coding |
27634902 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
PDCD4 is a direct target of miR-208a-3p |
target |
- |
- |
- |
PDCD4 |
protein-coding |
27634902 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
PDCD4 inhabit the development of tumor growth |
target |
- |
- |
- |
PIK3R1 |
protein-coding |
30927924 |
qRT-PCR |
tissue |
China |
44 |
- |
- |
- |
No Reports |
PIK3R1 was upregulated in DDP-resistant GC tissues samples when compared with CDDP-senestive groups. |
target |
- |
- |
- |
PIK3R1 |
protein-coding |
30927924 |
Western blot |
cell line |
- |
- |
- |
- |
- |
No Reports |
CDDP-resistant GC cells showed obvious increases in the expression of PIK3R1 mRNA and protein levels. |
target |
- |
- |
- |
PIK3R1 |
protein-coding |
30927924 |
Luciferase reporter assay; Western blot; qRT-PCR |
cell line |
- |
- |
- |
- |
- |
No Reports |
PIK3R1 is a direct target of miR-198; miR-198 mimics significantly inhibited PIK3R1 mRNA and protein levels and that ectopic PIK3R1 expression abolished the influence caused by miR-198 overexpression. |
target |
- |
- |
- |
PKM |
protein-coding |
28588255 |
IHC |
tissue |
China |
88 |
88 |
Up |
- |
No Reports |
PKM2 protein was predominantly located in the nucleus and cytoplasma, and was observed to have higher IHC scores in gastric cancer samples than in peritumor tissues; PKM2 expression was positively correlated with lymph node metastasis, tumor invasion and TNM staging. |
target/prognosis |
0.006 |
- |
- |
PKM |
protein-coding |
28588255 |
Cell proliferation assay; Cell colony formation assay; Invasion and migration assays; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
knockdown of PKM2 can inhibit GC cell proliferation, G1-S phase transition,especially, attenuate GC cell migration |
target/prognosis |
0.006 |
- |
- |
PKM |
protein-coding |
28588255 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
PKM2 knockdown inhibits the tumor progression of GC in vivo. |
target/prognosis |
0.006 |
- |
- |
PKM |
protein-coding |
28588255 |
Western blot; cell transduction |
cell line |
- |
- |
- |
- |
- |
No Reports |
PKM2 mediates cell migration and autophagy via the PI3K/Akt signaling pathway. |
target/prognosis |
0.006 |
- |
- |
RASSF1 |
protein-coding |
26735582 |
qRT-PCR |
tissue |
China |
28 |
28 |
Down |
- |
No Reports |
The expression of RASSF1A was lower in the cancer tissues than in the normal tissues. |
target |
- |
- |
- |
RASSF1 |
protein-coding |
26735582 |
Cell proliferation assay; Invasion and migration assays; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
The expression of RASSF1A could suppress the viability, migration and invasion capacity of SGC-7901 cell in vitro. |
target |
- |
- |
- |
RASSF1 |
protein-coding |
26735582 |
miRNA microarray; qRT-PCR |
cell line |
- |
- |
- |
- |
- |
No Reports |
The expression of miR-711 was higher in the pcDNA3.1-RASSF1A-transfected SGC-7901 cells than in the pcDNA3.1-vector-transfected SGC-7901 cells. |
target |
- |
- |
- |
SFRP1 |
protein-coding |
29886152 |
Cell proliferation assay; Cell invasion assay; |
cell line |
- |
- |
- |
- |
- |
No Reports |
SFRP1 partially reverses the effects of miR-208a on proliferation and invasion in GC |
target |
- |
- |
- |
SFRP1 |
protein-coding |
29886152 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
SFRP1 is a direct target of MiR-208a in GC cells |
target |
- |
- |
- |
SIRT1 |
protein-coding |
30250020 |
Cell invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
knockdown of SIRT1 promoted GC cell migration and invasion in vitro and metastasis in vivo. Forced expression of SIRT1 in GC cells had the opposite effects. SIRT1 inhibited the expression of ARHGAP5 by physically associating with transcription factor c-JUN and deacetylating and inhibiting the transcriptional activity of c-JUN. |
target |
- |
- |
- |
SIRT1 |
protein-coding |
30250020 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
SIRT1 inhibits metastasis of GC in vivo |
target |
- |
- |
- |
SIRT1 |
protein-coding |
30250020 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
SIRT1 inhibits expression of ARHGAP5 by physically interacting with and deacetylating c-JUN |
target |
- |
- |
- |
SKP2 |
protein-coding |
27572672 |
Western blot |
tissue |
China |
47 |
19 |
Up |
- |
No Reports |
The expression levels of Skp2 in the gastric cancer tissues were significantly increased, compared with those in the normal gastric tissues |
target |
- |
- |
- |
SKP2 |
protein-coding |
27572672 |
Cell proliferation assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Defective regulation of Skp2 or the presence of Skp2 inhibitor contribute to decreased proliferation in human gastric cancer cell lines.Skp2 inhibitor inhibits the proliferation of gastric cancer cells in a dose‑dependent manner |
target |
- |
- |
- |
SKP2 |
protein-coding |
27572672 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
Interference with the endogenous expression of Skp2 inhibits tumor cell growth in nude mice. |
target |
- |
- |
- |
SNHG7 |
lncRNA |
29131253 |
qRT-PCR |
tissue |
China |
68 |
68 |
Up |
- |
No Reports |
The qRT-PCR experiment showed that in a total of 68 cases of cancer tissues and tumor-adjacent tissues, the relative expression of SNHG7 was upregulated in 48 cases of gastric cancer tissues and 5 gastric cancer cell lines. |
target |
- |
- |
- |
SNHG7 |
lncRNA |
29131253 |
Cell proliferation assay; Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
The in vitro experiments showed that after SNHG7 expression was interfered, the proliferation of gastric cancer cells was inhibited with an increase in apoptotic rate and arrest of cell cycle in G1/G0 phase. |
target |
- |
- |
- |
SNHG7 |
lncRNA |
29131253 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
Experiment on nude-mouse transplanted tumor model confirmed that after SNHG7 expression was interfered, in vivo tumor growth was inhibited. |
target |
- |
- |
- |
SNORD105B |
snoRNA |
29554660 |
qRT-PCR |
tissue |
China |
109 |
109 |
Up |
- |
No Reports |
The snord105b was upregulated in GC tissues and associated with tumor size, differentiation, and pathological stage in GC. |
target |
- |
- |
- |
SNORD105B |
snoRNA |
29554660 |
qRT-PCR |
serum |
China |
68 |
25 |
Up |
- |
No Reports |
The snord105b was upregulated in GC serum samples when compared with healthy donors. |
target |
- |
- |
- |
SNORD105B |
snoRNA |
29554660 |
Cell proliferation assay; Invasion and migration assay; Clonogenic assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
Snord105b promotes the proliferation, migration,invasion and clonogenictiy in multiple GC cell lines. The oncoqenic activity of snord105b was also confirmed with in vivo data. Mechanistically, snord105b specifically bound to ALDOA and affected C-myc, which plays a key role in carcinogenesis and tumor development. |
target |
- |
- |
- |
SNORD105B |
snoRNA |
29554660 |
RIP assay; CHIRP-MS |
cell line |
- |
- |
- |
- |
- |
No Reports |
Snord105b is associated with the ALDOA protein |
target |
- |
- |
- |
SNORD105B |
snoRNA |
29554660 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
Promotes the growth of transplanted tumors in vivo. |
target |
- |
- |
- |
SUFU |
protein-coding |
27810403 |
Luciferase reporter assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
SUFU is the functional target of miRNA-194 |
target |
- |
- |
- |
SUFU |
protein-coding |
27810403 |
IHC |
tissue |
China |
75 |
75 |
Down |
- |
No Reports |
SUFU was significantly down expressed in GCs compared to NSs. The expression level of SUFU was negatively associated with tumor stage. |
target |
- |
- |
- |
SUFU |
protein-coding |
27810403 |
qRT-PCR |
tissue |
China |
20 |
20 |
Down |
- |
No Reports |
SUFU mRNA was significantly down expressed in GCs; a negative relationship between miRNA-194 and SUFU expression levels |
target |
- |
- |
- |
TMEM41A |
protein-coding |
30015937 |
qRT-PCR |
tissue |
China |
147 |
147 |
Up |
Up |
No Reports |
TMEM41A was highly expressed in GC tissues, its expression of TMEM41A was observed to be correlated with lymph node metastasis, distant metastasis and advanced tumor, node and metastasis stages.Patients with GC and high expression levels of TMEM41A exhibited a poorer disease‑free survival following radical tumor resection. |
target |
- |
- |
- |
TMEM41A |
protein-coding |
30015937 |
Cell proliferation assay; Invasion and migration assays; Cell immunofluorescence for cytoskeleton stain and autophagy |
cell line |
- |
- |
- |
- |
- |
No Reports |
Knockdown of TMEM41A in vitro decreased the GC cell migration ability by regulating epithelial-to-mesenchymal transition and cell autophagy, via the upregulation of E-cadherin and downregulating N-cadherin expression in GC cells. |
target |
- |
- |
- |
TMEM41A |
protein-coding |
30015937 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
Knockdown of TMEM41A was also observed to affect tumor metastasis in nude mice. |
target |
- |
- |
- |
TNK2 |
protein-coding |
25678401 |
Western blot |
tissue |
China |
6 |
6 |
Up |
- |
No Reports |
ACK1 protein level and ACK1 phosphorylation at Tyr 284 were frequently elevated in GC tissues. |
target/prognosis |
< 0.001 |
- |
- |
TNK2 |
protein-coding |
25678401 |
IHC |
tissue |
China |
77 |
77 |
Up |
- |
No Reports |
ACK1 overexpression in GC correlates with poor prognosis; positively associated with lymph node metastasis and a more advanced clinical stage in GC |
target/prognosis |
< 0.001 |
- |
- |
TNK2 |
protein-coding |
25678401 |
Cell invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
ACK1 induces EMT, invasion, and metastasis |
target/prognosis |
< 0.001 |
- |
- |
TNK2 |
protein-coding |
25678401 |
Western blot; Luciferase reporter assay; IHC |
cell line |
- |
- |
- |
- |
- |
No Reports |
ACK1 up-regulates ECD expression by increasing the level of POU2F1. |
target/prognosis |
< 0.001 |
- |
- |
UCA1 |
lncRNA |
28569779 |
qRT-PCR |
tissue |
China |
39 |
39 |
Up |
- |
No Reports |
UCA1 expressed highly in GC tissues and GC cells, overexpression of UCA1 indicated higher tumor stage and lymph node metastasis in GC patients. |
target |
- |
- |
- |
YBX1 |
protein-coding |
25959498 |
RNA pull-down assay |
cell line |
- |
- |
- |
- |
- |
No Reports |
lncRNA GAS5 interacts with the transcriptional activator YBX1. |
target |
- |
- |
- |
YBX1 |
protein-coding |
25959498 |
Flow cytometry |
cell line |
- |
- |
- |
- |
- |
No Reports |
YBX1 depletion reduces G1 phase arrest by decreasing p21 expression. |
target |
- |
- |
- |
ZNF143 |
protein-coding |
27449034 |
qRT-PCR |
tissue |
China |
53 |
53 |
Up |
- |
No Reports |
ZNF143 level is upregulated in gastric cancer and highly correlated with the presence of lymph node metastasis. |
target |
- |
- |
- |
ZNF143 |
protein-coding |
27449034 |
IHC |
tissue |
China |
12 |
12 |
Up |
- |
No Reports |
Protein level of ZNF143 is higher in GC tssues and staining in the nucleus of GC cells |
target |
- |
- |
- |
ZNF143 |
protein-coding |
27449034 |
Cell invasion and migration assays |
cell line |
- |
- |
- |
- |
- |
No Reports |
ZNF143 knockdown inhibits the migration and invasion of gastric cancer cells, and overexpression contributes to the migration and invasion of GC cells. |
target |
- |
- |
- |
ZNF143 |
protein-coding |
27449034 |
Xenograft mice models |
mice |
- |
- |
- |
- |
- |
No Reports |
ZNF143 knockdown suppresses metastases of GC cells in vivo |
target |
- |
- |
- |
ZNF143 |
protein-coding |
27449034 |
Western blot; cell transfection |
cell line |
- |
- |
- |
- |
- |
No Reports |
Overexpression of ZNF143 re- duced the expression of epithelial cell marker (E-cadherin) and induced the expression mesenchymal cell marker (N-cadherin, Vimentin), related transcription factors (snail, slug), and upregulated the expression of phosphorylation AKT. |
target |
- |
- |
- |