MIR5582 Gene

Name microRNA 5582
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": "\nCurrent research into noncoding RNAs and their influence on cancer biology has uncovered a complex regulatory network in which diverse RNA species contribute to tumor behavior. In an investigation of breast cancer stem cell characteristics, long noncoding RNAs were shown to play pivotal roles, raising the possibility that related noncoding molecules, such as MIR5582, may also participate in the regulation of cancer stemness and differentiation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFunctional studies focusing directly on MIR5582 have revealed its tumor suppressive properties in different malignancies. One study demonstrated that miR-5582-5p induces apoptosis and triggers cell cycle arrest by directly targeting regulators including GAB1, SHC1, and CDK2, ultimately suppressing tumor growth in xenograft models. Similarly, another investigation found that hsa-miR-5582-3P downregulates the TGFβ/SMAD signaling pathway through direct interaction with the 3′ untranslated regions of TGFβ-R1, TGFβ-R2, SMAD3, and SMAD4, thereby inhibiting cancer cell proliferation and inducing cell cycle arrest."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its role in tumor suppression, emerging evidence regarding the genomic linkage between intronic microRNAs and their host genes in cardiovascular disease suggests that MIR5582 may have broader implications in modulating gene networks associated with cardiovascular pathology. Although these cardiovascular insights are preliminary, they underscore the potential of MIR5582 as part of a larger regulatory paradigm that spans both oncological and cardiovascular contexts."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Ang Zheng, Xinyue Song, Lin Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Long non-coding RNA LUCAT1/miR-5582-3p/TCF7L2 axis regulates breast cancer stemness via Wnt/β-catenin pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Exp Clin Cancer Res (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s13046-019-1315-8"}], "href": "https://doi.org/10.1186/s13046-019-1315-8"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31300015"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31300015"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Hyun-Ju An, Seo-Young Kwak, Je-Ok Yoo, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Novel miR-5582-5p functions as a tumor suppressor by inducing apoptosis and cell cycle arrest in cancer cells through direct targeting of GAB1, SHC1, and CDK2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochim Biophys Acta (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbadis.2016.07.017"}], "href": "https://doi.org/10.1016/j.bbadis.2016.07.017"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27475256"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27475256"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Elham Abedini Bakhshmand, Bahram Mohammad Soltani, Ali Fasihi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Hsa-miR-5582-3P regulatory effect on TGFβ signaling through targeting of TGFβ-R1, TGFβ-R2, SMAD3, and SMAD4 transcripts."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biochem (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcb.27314"}], "href": "https://doi.org/10.1002/jcb.27314"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30129155"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30129155"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Yan Zhu, Jingjing Xie, Hong Sun "}, {"type": "b", "children": [{"type": "t", "text": "Three miRNAs cooperate with host genes involved in human cardiovascular disease."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Genomics (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1186/s40246-019-0232-4"}], "href": "https://doi.org/10.1186/s40246-019-0232-4"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31464655"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31464655"}]}]}]}
NCBI Gene ID 100847020
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Download Associations
Predicted Functions View MIR5582's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR5582's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR5582's ARCHS4 Predicted Functions.

Functional Associations

MIR5582 has 157 functional associations with biological entities spanning 2 categories (cell line, cell type or tissue, gene, protein or microRNA) extracted from 4 datasets.

Click the + buttons to view associations for MIR5582 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 MIR5582 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 MIR5582 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR5582 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 MIR5582 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset.