MKGC: a curated molecular knowledgebase for gastric cancer


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Gene Summary for MIR874 Gene

Official Symbol MIR874 Gene Type miRNA
Full Name microRNA 874 Entrez 100126343
Ensembl ID ENSG00000216009 HGNC 33643
Aliases MIRN874, hsa-mir-874, mir-874 Chromosome Location Chromosome 5, NC_000005.10 (137647572..137647649, 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 MIR874 Gene

PMID Author Year ID in Paper
Conclusion
23800944 Baofei Jiang 2014 miR-874 AQP3 is upregulated, as well as highlight the importance of miR-874 in gastric cancer development and progression.

Experiment for MIR874 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 75 75 qRT-PCR China No Reports Down Down - miR-874 was significantly down-regulated and reversely correlated with AQP3 protein levels in clinical samples. miR-874 expression level was lower in samples with moderately and poorly histological type, lymph node metastasis N1-N3 and stage III–IV. Analysis of the clinicopathological significance showed that miR-874 and AQP3 were closely correlated with GC characteristics. 23800944
cell line - - Cell proliferation assay; Invasion and migration assays; Flow Cytometry - No Reports - - Functional analyses indicated that ectopic miR-874 expression suppressed the growth, migration, invasion and tumorigenicity of GC cells, whereas miR-874 knockdown promoted these phenotypes. Down-regulation of Bcl-2, MT1-MMP, MMP-2 and MMP-9 and upregulation of caspase-3 activity and Bax were involved in miR-874 inducing cell apoptosis, and inhibiting migration and invasion. Functional analyses indicated that ectopic miR-874 expression suppressed the growth, migration, invasion and tumorigenicity of GC cells, whereas miR-874 knockdown promoted these phenotypes. Down-regulation of Bcl-2, MT1-MMP, MMP-2 and MMP-9 and upregulation of caspase-3 activity and Bax were involved in miR-874 inducing cell apoptosis, and inhibiting migration and invasion. 23800944
mice - - Xenograft mice models - No Reports - - - miR-874 suppresses the tumorigenicity in vivo 23800944
cell line - - Luciferase reporter assay - No Reports - - - miR-874 directly interacts with a putative binding site of AQP3-3'UTR 23800944

Function for MIR874 Gene

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

Interaction for MIR874 Gene

Interaction Gene Method PMID
AQP3 Luciferase reporter assay 23800944
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