| HGNC Family | Non-coding RNAs |
| Name | microRNA 892b |
| Description | 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] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nRecent studies in pancreatic ductal adenocarcinoma (PDAC) have shown that an oncogenic circular RNA, circ_0007534, promotes tumorigenesis in part by sponging microRNAs such as miR‑892b. This interaction diminishes the availability of miR‑892b to regulate its target genes, thereby contributing to enhanced proliferation, migration, invasion, and decreased apoptosis in PDAC cells."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn the setting of metabolic disorders, circulating levels of miR‑892b have been found to be significantly elevated in patients with type 2 diabetes mellitus and even more so in those with microvascular complications. This upregulation suggests that miR‑892b may serve as an auxiliary biomarker and potential risk factor for diabetic-associated vascular pathology."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn breast cancer, miR‑892b acts as a tumor suppressor whose expression is notably downregulated in tumor tissues, a reduction that correlates with poor patient outcomes. Experimental overexpression of miR‑892b suppresses tumor growth, metastasis, and angiogenesis by directly targeting several key mediators of the NF‑κB signaling cascade—including TRAF2, TAK1, and TAB3—thus mitigating the sustained activation of this pro‐tumorigenic pathway."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nSimilarly, functional investigations in bladder cancer have demonstrated that miR‑892b inhibits cell proliferation, migration, and invasion. Its overexpression induces G1 phase cell cycle arrest and modulates critical pathways via downregulation of cyclin D1 and CDK6, accompanied by upregulation of p19ARF, as well as suppression of MMP‑9 expression through effects on Sp‑1 transcription factor activity. These findings highlight miR‑892b’s therapeutic potential as an inhibitor of tumor progression in advanced bladder cancers."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Liguo Hao, Wei Rong, Lianjie Bai, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Upregulated circular RNA circ_0007534 indicates an unfavorable prognosis in pancreatic ductal adenocarcinoma and regulates cell proliferation, apoptosis, and invasion by sponging miR-625 and miR-892b."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biochem (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcb.27658"}], "href": "https://doi.org/10.1002/jcb.27658"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30382592"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30382592"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Cheng Wang, Shujun Wan, Ting Yang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Increased serum microRNAs are closely associated with the presence of microvascular complications in type 2 diabetes mellitus."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/srep20032"}], "href": "https://doi.org/10.1038/srep20032"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26831044"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26831044"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Lili Jiang, Liang Yu, Xin Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "miR-892b Silencing Activates NF-κB and Promotes Aggressiveness in Breast Cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cancer Res (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1158/0008-5472.CAN-15-1770"}], "href": "https://doi.org/10.1158/0008-5472.CAN-15-1770"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26747895"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26747895"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Seung-Shick Shin, Sung-Soo Park, Byungdoo Hwang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MicroRNA-892b influences proliferation, migration and invasion of bladder cancer cells by mediating the p19ARF/cyclin D1/CDK6 and Sp-1/MMP-9 pathways."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncol Rep (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3892/or.2016.5052"}], "href": "https://doi.org/10.3892/or.2016.5052"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27573859"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27573859"}]}]}]}
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| Synonyms | MIRN892B |
| NCBI Gene ID | 100126307 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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MIR892B has 160 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 10 datasets.
Click the + buttons to view associations for MIR892B from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CCLE Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR892B gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR892B gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. | |
| ENCODE Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR892B gene from the ENCODE Histone Modification Site Profiles dataset. | |
| ENCODE Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR892B gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR892B gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| GEO Signatures of Differentially Expressed Genes for Gene Perturbations | gene perturbations changing expression of MIR892B gene from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. | |
| JASPAR Predicted Transcription Factor Targets | transcription factors regulating expression of MIR892B gene predicted using known transcription factor binding site motifs from the JASPAR Predicted Transcription Factor Targets dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR892B gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| MotifMap Predicted Transcription Factor Targets | transcription factors regulating expression of MIR892B gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset. | |
| Roadmap Epigenomics Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR892B gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |