| HGNC Family | Non-coding RNAs |
| Name | microRNA 4262 |
| 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": "\nmiR‐4262 has been implicated in multiple malignancies with seemingly divergent roles. In osteosarcoma, reduced expression of miR‐4262 is associated with increased osteopontin levels, enhanced cancer cell invasion, and poorer patient survival, suggesting that miR‐4262 normally functions to restrain OPN‐mediated invasion by directly targeting OPN mRNA (see."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " In hepatocellular carcinoma, miR‐4262 is overexpressed and promotes cell cycle progression and proliferation via direct inhibition of the tumor suppressor PDCD4 and activation of NF‐κB signaling."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " Likewise, in breast cancer, elevated miR‐4262 levels enhance cellular proliferation and invasion by targeting the tumor suppressors KLF6 and KLF15."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn contrast, in colon and cervical cancers, miR‐4262 acts as a tumor suppressor. In colon cancer cell models, overexpression of miR‐4262 decreases the expression of GALNT4, leading to suppressed cell viability, growth, and cell‐cycle progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": " Similarly, in cervical cancer, miR‐4262 is downregulated and its enforced expression inhibits proliferation and epithelial–mesenchymal transition (EMT) by directly downregulating the transcription factor Kaiso."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": " In nasopharyngeal carcinoma, although miR‐4262 levels are lower compared to adjacent tissues, restoration of miR‐4262 negatively regulates GRP78, contributing to reduced cellular proliferation and enhanced apoptosis, which was also reflected in xenograft models."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAdditional studies reveal a context‐dependent oncogenic potential of miR‐4262. In cutaneous malignant melanoma, miR‐4262 is upregulated where it targets KLF6 and, through subsequent modulation of EGFR activation and p21 expression, drives melanoma cell proliferation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": " In an acute lung injury model, the long non‐coding RNA MEG3 acts as a sponge for miR‐4262, and MEG3 knockdown aggravates LPS-induced lung cell injury by permitting miR‐4262–mediated downregulation of KLF4, implicating miR‐4262 in lung cell apoptosis and impaired cell survival."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "8"}]}, {"type": "t", "text": " Furthermore, preliminary data in glioma suggest that miR‐4262 may promote proliferation and migration"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "9"}]}, {"type": "t", "text": ", while ongoing investigations in esophageal cancer aim to establish its expression patterns and prognostic significance."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "10"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Kun Song, Ning Liu, Yan Yang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Regulation of osteosarcoma cell invasion through osteopontin modification by miR-4262."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Tumour Biol (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s13277-015-4530-8"}], "href": "https://doi.org/10.1007/s13277-015-4530-8"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26634745"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26634745"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Sen Lu, Jindao Wu, Yuanyuan Gao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MicroRNA-4262 activates the NF-κB and enhances the proliferation of hepatocellular carcinoma cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Biol Macromol (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ijbiomac.2016.01.019"}], "href": "https://doi.org/10.1016/j.ijbiomac.2016.01.019"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26778158"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26778158"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Ke Wang, Yu Ren, Yang Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "miR-4262 Promotes Proliferation and Invasion of Human Breast Cancer Cells Through Directly Targeting KLF6 and KLF15."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncol Res (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3727/096504016X14732514133203"}], "href": "https://doi.org/10.3727/096504016X14732514133203"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27629257"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27629257"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Jian-Jun Qu, Xiang-Yang Qu, De-Zhen Zhou "}, {"type": "b", "children": [{"type": "t", "text": "miR‑4262 inhibits colon cancer cell proliferation via targeting of GALNT4."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Med Rep (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3892/mmr.2017.7057"}], "href": "https://doi.org/10.3892/mmr.2017.7057"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28731150"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28731150"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Jing Feng "}, {"type": "b", "children": [{"type": "t", "text": "Upregulation of MicroRNA-4262 Targets Kaiso (ZBTB33) to Inhibit the Proliferation and EMT of Cervical Cancer Cells."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncol Res (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3727/096504017X15021536183526"}], "href": "https://doi.org/10.3727/096504017X15021536183526"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28800784"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28800784"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Shaosheng Liu, Yuanyuan Li, Zhaoxia Li "}, {"type": "b", "children": [{"type": "t", "text": "Salidroside suppresses the activation of nasopharyngeal carcinoma cells via targeting miR-4262/GRP78 axis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Cycle (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/15384101.2021.2019976"}], "href": "https://doi.org/10.1080/15384101.2021.2019976"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35220889"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35220889"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Dingwei Zhang, Zhangjun Li, Yanfei Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "miR-4262 promotes the proliferation of human cutaneous malignant melanoma cells through KLF6-mediated EGFR inactivation and p21 upregulation."}]}, {"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.2016.5190"}], "href": "https://doi.org/10.3892/or.2016.5190"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27779691"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27779691"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Xiaoliang Li, Qianqian Zhang, Zhigang Yang "}, {"type": "b", "children": [{"type": "t", "text": "Silence of MEG3 intensifies lipopolysaccharide-stimulated damage of human lung cells through modulating miR-4262."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Artif Cells Nanomed Biotechnol (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/21691401.2019.1623233"}], "href": "https://doi.org/10.1080/21691401.2019.1623233"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31184231"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31184231"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Chunbo Liu, Tao Ma, Tianwei Jiang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Abnormal increase of miR-4262 promotes cell proliferation and migration by targeting large tumor suppressor 1 in gliomas."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Pathol Res Pract (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.prp.2019.152778"}], "href": "https://doi.org/10.1016/j.prp.2019.152778"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31831299"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31831299"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Zhanye Liu, Chunlong Zhao, Shixia Du, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-4262 inhibits the development of esophageal cancer by negatively regulating KLF6 level."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Exp Mol Pathol (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.yexmp.2020.104476"}], "href": "https://doi.org/10.1016/j.yexmp.2020.104476"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32473153"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32473153"}]}]}]}
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| NCBI Gene ID | 100422996 |
| 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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MIR4262 has 367 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 11 datasets.
Click the + buttons to view associations for MIR4262 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 MIR4262 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| ChEA Transcription Factor Binding Site Profiles | transcription factor binding site profiles with transcription factor binding evidence at the promoter of MIR4262 gene from the CHEA Transcription Factor Binding Site Profiles dataset. | |
| ChEA Transcription Factor Targets | transcription factors binding the promoter of MIR4262 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR4262 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 MIR4262 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 MIR4262 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR4262 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| JASPAR Predicted Transcription Factor Targets | transcription factors regulating expression of MIR4262 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 MIR4262 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 MIR4262 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 MIR4262 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |