| HGNC Family | Non-coding RNAs |
| Name | microRNA 1180 |
| 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": "\nIn hepatocellular carcinoma (HCC), miR‑1180 is markedly upregulated and acts in an oncogenic manner. Its increased expression confers resistance to apoptosis by directly downregulating multiple key regulators, including inhibitors of the nuclear factor‐κB (NF‑κB) pathway (OTUD7B and TNIP2) as well as the pro‑apoptotic protein BAD, thereby promoting NF‑κB pathway activation and tumor cell survival. In addition, miR‑1180 enhances cell proliferation by suppressing TNIP2, and its expression correlates with poor clinical outcomes and enrichment of cancer‑related signaling cascades such as Ras and MAPK. A DNA methylation–mediated competing endogenous RNA (ceRNA) network involving miR‑1180 further underscores its role in HCC tumorigenesis."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn contrast, in bladder cancer, miR‑1180‑5p expression is significantly reduced compared with normal urothelial cells. Restoration of miR‑1180‑5p levels induces the tumor-suppressive gene p21, leading to cell cycle arrest through the downregulation of cyclin-dependent kinases (CDK4 and CDK6) and cyclins (Cyclin D1 and Cyclin A2), which in turn suppresses cancer cell proliferation and tumor growth in vivo."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nSimilarly, in colorectal cancer (CRC), miR‑1180‑3p is downregulated in patient tissues, blood, and cell lines relative to normal counterparts. Lower miR‑1180‑3p levels are significantly associated with features of aggressiveness, such as vascular invasion, lymph node metastasis, and advanced TNM stage, while its overexpression reduces cell proliferation and migratory capacity and promotes apoptosis via targeting COL12A1. These findings support a tumor‑suppressive role for miR‑1180‑3p in CRC and highlight its potential as a diagnostic and prognostic biomarker."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Guosheng Tan, Linwei Wu, Jinfu Tan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-1180 promotes apoptotic resistance to human hepatocellular carcinoma via activation of NF-κB signaling pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/srep22328"}], "href": "https://doi.org/10.1038/srep22328"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26928365"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26928365"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Xu Zhou, Hua-Qiang Zhu, Chao-Qun Ma, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-1180 promoted the proliferation of hepatocellular carcinoma cells by repressing TNIP2 expression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biomed Pharmacother (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biopha.2016.02.025"}], "href": "https://doi.org/10.1016/j.biopha.2016.02.025"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27044843"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27044843"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Z H Zhou, X G Zhou, Z W Zhou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "[Integrated analysis of DNA methylation and gene expression profiles of hepatocellular carcinoma to construct miR-1180-3p relevant ceRNA regulatory network]."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Zhonghua Gan Zang Bing Za Zhi (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3760/cma.j.cn501113-20200103-00003"}], "href": "https://doi.org/10.3760/cma.j.cn501113-20200103-00003"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32660176"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32660176"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Zihan Zhou, Xianguo Zhou, Yanji Jiang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Clinical significance of miR-1180-3p in hepatocellular carcinoma: a study based on bioinformatics analysis and RT-qPCR validation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41598-020-68450-z"}], "href": "https://doi.org/10.1038/s41598-020-68450-z"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32665670"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32665670"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Qiangqiang Ge, Chenghe Wang, Zhong Chen, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The suppressive effects of miR-1180-5p on the proliferation and tumorigenicity of bladder cancer cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Histol Histopathol (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.14670/HH-11-772"}], "href": "https://doi.org/10.14670/HH-11-772"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27112784"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27112784"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Chunlei Li, Wei Jin, Dewei Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Clinical significance of microRNA-1180-3p for colorectal cancer and effect of its alteration on cell function."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Bioengineered (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/21655979.2021.1997694"}], "href": "https://doi.org/10.1080/21655979.2021.1997694"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34723759"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34723759"}]}]}]}
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| Synonyms | HSA-MIR-1180, MIR-1180, MIRN1180 |
| NCBI Gene ID | 100302256 |
| 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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MIR1180 has 324 functional associations with biological entities spanning 4 categories (molecular profile, chemical, cell line, cell type or tissue, gene, protein or microRNA) extracted from 11 datasets.
Click the + buttons to view associations for MIR1180 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 MIR1180 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 MIR1180 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. | |
| CTD Gene-Chemical Interactions | chemicals interacting with MIR1180 gene/protein from the curated CTD Gene-Chemical Interactions dataset. | |
| ENCODE Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR1180 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 MIR1180 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR1180 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| JASPAR Predicted Transcription Factor Targets | transcription factors regulating expression of MIR1180 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 MIR1180 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 MIR1180 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset. | |
| Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles | cell types and tissues with high or low DNA methylation of MIR1180 gene relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. | |
| Roadmap Epigenomics Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR1180 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |