| HGNC Family | Non-coding RNAs |
| Name | microRNA 524 |
| 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 various malignancies, miR-524‐5p functions as a potent tumor suppressor by directly targeting critical components of oncogenic signaling pathways. In glioma, it inhibits Notch signaling through suppression of key effectors (e.g., Jagged‐1 and Hes‐1)."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " In melanoma, miR-524-5p directly binds to the MAPK/ERK regulators, BRAF and ERK2, thereby restraining cell proliferation and invasion."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " In glioblastoma, both miR-524-3p and miR-524-5p isoforms attenuate multiple tumor‐promoting cascades—including the TGF-β, Notch, and Hippo pathways—by targeting molecules such as Smad2, Hes1, and Tead1."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": " In papillary thyroid cancer, direct targeting of FOXE1 and ITGA3 disrupts cell cycle progression and autophagy, thereby impeding tumor growth."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": " Moreover, in oral squamous cell carcinoma, reduced miR-524-5p expression is associated with enhanced tumor progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nmiR-524-5p also plays a crucial role in modulating chemoresistance and the tumor microenvironment. In gastric cancer, its downregulation correlates with increased chemoresistance and aggressiveness through aberrant regulation of SOX9."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": " In ameloblastoma, lower miR-524-5p levels are linked to an upregulation of the IL-33/ST2 axis, a change that contributes to a tumor-supportive immune milieu."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "9"}]}, {"type": "t", "text": " In colon cancer, miR-524-5p directly targets WNK1, leading to suppression of angiogenesis"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "10"}]}, {"type": "t", "text": ", while in breast cancer its inhibitory effect on FSTL1 curtails cell migration, invasion, and the epithelial-to-mesenchymal transition."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "11"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond these roles, miR-524-5p is implicated in cellular reprogramming and in controlling metastatic progression. It enhances the efficiency of induced pluripotent stem cell generation"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "12"}]}, {"type": "t", "text": "and helps restore drug sensitivity in BRAF inhibitor–resistant melanoma."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " In preeclampsia, miR-524-5p promotes trophoblast proliferation and invasion by targeting NUMB to modulate Notch signaling"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "13"}]}, {"type": "t", "text": ", and in triple-negative breast cancer, sequestration of miR-524-5p by the lncRNA SChLAP1 leads to upregulation of HMGA2 and enhanced malignancy."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "14"}]}, {"type": "t", "text": " In non-small cell lung cancer, binding of miR-524-5p by LINC00184 results in increased HMGB2 expression and tumor progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "15"}]}, {"type": "t", "text": " Similarly, in laryngocarcinoma, NEAT1 acts as a competing endogenous RNA to sponge miR-524-5p, thereby promoting HDAC1 expression and activating the PTEN/AKT pathway."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "16"}]}, {"type": "t", "text": " In chondrosarcoma, the YAP/miR-524-5p/TXNIP signaling axis modulates glycolytic metabolism and cell proliferation"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "17"}]}, {"type": "t", "text": ", while in papillary thyroid carcinoma, NEAT1 regulates the miR-524-5p/ID1 axis to facilitate tumor growth."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "18"}]}, {"type": "t", "text": " Finally, in bone metastases from prostate and breast cancers, miR-524-5p targets MEF2C to restrict metastatic dissemination."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "19"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Lingchao Chen, Wei Zhang, Wei Yan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The putative tumor suppressor miR-524-5p directly targets Jagged-1 and Hes-1 in glioma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Carcinogenesis (2012)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/carcin/bgs261"}], "href": "https://doi.org/10.1093/carcin/bgs261"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "22871495"}], "href": "https://pubmed.ncbi.nlm.nih.gov/22871495"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Szu-Mam Liu, Jean Lu, Hoong-Chien Lee, et al. 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| Synonyms | MIR-524, HSA-MIR-524, MIRN524 |
| NCBI Gene ID | 574478 |
| 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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MIR524 has 188 functional associations with biological entities spanning 4 categories (molecular profile, functional term, phrase or reference, cell line, cell type or tissue, gene, protein or microRNA) extracted from 12 datasets.
Click the + buttons to view associations for MIR524 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 MIR524 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 MIR524 gene from the CHEA Transcription Factor Binding Site Profiles dataset. | |
| ChEA Transcription Factor Targets | transcription factors binding the promoter of MIR524 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 MIR524 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 MIR524 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 MIR524 gene from the ENCODE Transcription Factor Binding Site Profiles dataset. | |
| ENCODE Transcription Factor Targets | transcription factors binding the promoter of MIR524 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset. | |
| GeneRIF Biological Term Annotations | biological terms co-occuring with MIR524 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. | |
| GeneSigDB Published Gene Signatures | PubMedIDs of publications reporting gene signatures containing MIR524 from the GeneSigDB Published Gene Signatures dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR524 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| KnockTF Gene Expression Profiles with Transcription Factor Perturbations | transcription factor perturbations changing expression of MIR524 gene from the KnockTF Gene Expression Profiles with Transcription Factor Perturbations dataset. | |
| Roadmap Epigenomics Histone Modification Site Profiles | histone modification site profiles with high histone modification abundance at MIR524 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset. | |