MIR4270 Gene

HGNC Family Non-coding RNAs
Name microRNA 4270
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": "\nResearch into microRNA‐4270 (miR-4270) has revealed its multifaceted role in cancer biology, particularly in hepatocellular carcinoma (HCC). In HCC cells, overexpression of miR-4270-5p has been shown to suppress cell proliferation and invasion by directly targeting the transcriptional regulator SATB2, thereby reversing epithelial–mesenchymal transition and curbing tumor aggressiveness. These findings suggest that miR-4270 can function as a tumor suppressor and may offer prognostic and therapeutic potential in HCC."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn addition to its role in HCC, miR-4270 has been implicated in modulating the response to irradiation and metastatic behavior in other cancer models. In nasopharyngeal carcinoma, lower expression levels of miR-4270 (among the top differential microRNAs distinguishing radio-sensitive from radio-resistant patients) result in altered p53 regulation, where inhibition of miR-4270 increases cell sensitivity to irradiation. Furthermore, studies employing miR-4270 inhibitors in HepG2 cells have demonstrated decreased cell migration and matrix metalloproteinase activity, highlighting its potential involvement in metastasis suppression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond oncological contexts, miR-4270 also appears to play a role in inflammatory conditions. In rheumatoid arthritis, circulating levels of miR-4270 are significantly upregulated compared with healthy individuals, and its expression correlates with key metabolic and inflammatory markers. This association not only emphasizes the microRNA’s potential as a non-invasive biomarker for rheumatoid arthritis but also suggests that miR-4270 might serve as a molecular link between inflammation and metabolic disturbances."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Yun Wang, Chang-Feng Li, Li-Bo Sun, et al. "}, {"type": "b", "children": [{"type": "t", "text": "microRNA-4270-5p inhibits cancer cell proliferation and metastasis in hepatocellular carcinoma by targeting SATB2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Cell (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s13577-020-00384-0"}], "href": "https://doi.org/10.1007/s13577-020-00384-0"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32504285"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32504285"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Qiang Zou, Shasha Cao "}, {"type": "b", "children": [{"type": "t", "text": "miR-4270 suppresses hepatocellular carcinoma progression by inhibiting DNMT3A-mediated methylation of HGFAC promoter."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PeerJ (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.7717/peerj.16566"}], "href": "https://doi.org/10.7717/peerj.16566"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38077422"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38077422"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Wenwei Hao, Yongping Zhu, Haowei Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "miR-4270 Modulates the Irradiation-Sensitivity of Nasopharyngeal Carcinoma Cells through Modulation of p53 in Vivo."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Tohoku J Exp Med (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1620/tjem.254.63"}], "href": "https://doi.org/10.1620/tjem.254.63"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34078755"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34078755"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Hassan Akrami, Hanieh Gholami, Mohammad Reza Fattahi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Effect of miR-4270 Suppression on Migration in Hepatocellular Carcinoma Cell Line (HepG2)"}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Iran Biomed J (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.61186/ibj.3923"}], "href": "https://doi.org/10.61186/ibj.3923"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37430248"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37430248"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Sepideh Ghodoosifar, Gholamreza Dehghan, Reza Safaralizadeh, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The Association between the Expression of MicroRNA-4270 and MicroRNA-4441 with some Metabolic Factors in Iranian Rheumatoid Arthritis Patients."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Iran J Allergy Asthma Immunol (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.18502/ijaai.v22i6.14643"}], "href": "https://doi.org/10.18502/ijaai.v22i6.14643"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38477951"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38477951"}]}]}]}
NCBI Gene ID 100422868
API
Download Associations
Predicted Functions View MIR4270's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR4270's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR4270's ARCHS4 Predicted Functions.

Functional Associations

MIR4270 has 234 functional associations with biological entities spanning 3 categories (molecular profile, cell line, cell type or tissue, gene, protein or microRNA) extracted from 9 datasets.

Click the + buttons to view associations for MIR4270 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 MIR4270 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 MIR4270 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 MIR4270 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 MIR4270 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of MIR4270 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
JASPAR Predicted Transcription Factor Targets transcription factors regulating expression of MIR4270 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 MIR4270 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 MIR4270 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 MIR4270 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.