MKGC: a curated molecular knowledgebase for gastric cancer


Search Result

 

Gene Summary for MIR106B Gene

Official Symbol MIR106B Gene Type miRNA
Full Name microRNA 106b Entrez 406900
Ensembl ID ENSG00000208036 HGNC 31495
Aliases MIRN106B, mir-106b Chromosome Location Chromosome 7, NC_000007.14 (100093993..100094074, complement)
Expression -
Summary microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]

Paper for MIR106B Gene

PMID Author Year ID in Paper
Conclusion
30907988 Zhenglun Zhu 2019 miR-106b miR-106b was a potent factor of promoting metastasis of EGC. Moreover, miR-106b inhibitor exhibited anti-cancer characteristics both in vitro and in vivo. The identification of ALEX1 expression correlating to miR-106b highlighted the significance of ALEX1 in miR-106b inhibitor suppressed gastric cancer, suggesting ALEX1 was a direct target of miR-106b. In addition, down-regulation of miR-106b promoted apoptosis of gastric cancer cells through inhibiting JAK/STAT signaling pathway.
29434197 Xingchen Dong 2018 miR-106b Our results reveal a novel mechanism by which BRD4 regulates cancer cell proliferation by modulating the cellular senescence through E2F/miR-106b-5p/p21 axis and provide new insights into using BET inhibitors as potential anticancer drugs.

Experiment for MIR106B Gene

Sample Type Sample Number GC Sample Number nonGC Method Region Hpylori Normal vs. GC Early-stage vs. Advanced stage Biological Functions in GC Cells Result PMID
tissue 10 - qRT-PCR; FISH China No Reports - - - miR-106b was increased in the metastasis tissues compared with non-metastasis tissues. 30907988
cell line - - Cell invasion and migration assays - No Reports - - miR-106b inhibitor could promote the apoptosis of gastric cancer cells miR-106b inhibitor could promote the apoptosis of gastric cancer cells 30907988
cell line - - Luciferase reporter assay - No Reports - - - miR-106b targeted ALEX1 in gastric cancer cells 30907988
mice - - Xenograft mice models - No Reports - - - Down-regulation of miR-106b inhibited gastric cancer in vivo. 30907988
cell line - - Luciferase reporter assay; Immunoblotting - 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. 29434197

Function for MIR106B Gene

Functional Type AUC Overall Survival Disease-free Survival
mechanism - - -
target - - -

Interaction for MIR106B Gene

Interaction Gene Method PMID
ARMCX1 Luciferase reporter assay 30907988
About Us      Admin
备案/许可证编号:苏ICP备2021043822号