MIR758 Gene

HGNC Family Non-coding RNAs
Name microRNA 758
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": "\nRecent studies have revealed that miR‐758 (including its isoforms miR‐758‐3p and miR‐758‐5p) plays multifaceted roles in regulating both metabolic/differentiation processes and tumorigenesis. In the realm of metabolic regulation, miR‐758‐5p has been shown to reduce cholesterol accumulation in macrophage‐derived foam cells by directly targeting the scavenger receptor CD36, thereby modulating cholesterol uptake and offering promise for atherosclerotic vascular disease therapy."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " In addition, during osteogenic differentiation of periodontal ligament stem cells, miR‐758 is modulated by the long noncoding RNA ANCR and directly targets Notch2, contributing to the regulation of osteoblast differentiation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn various cancers, miR‐758 generally acts as a tumor suppressor by negatively regulating oncogenic signaling pathways. In hepatocellular carcinoma, up‐regulation of miR‐758‐3p suppresses cell proliferation, migration, and invasion through its direct inhibition of targets such as MDM2 and mTOR."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " In non‐small cell lung cancer, reduced miR‐758‐3p—as mediated by the oncogenic lncRNA DANCR—leads to increased malignant potential, whereas restoration of miR‐758‐3p directly targeting NUSAP1 inhibits cellular proliferation, migration, and invasion."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": " Further, in papillary thyroid cancer, miR‐758‐3p exerts antitumor effects by directly targeting TAB1"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": ", and in esophageal cancer, hypoxia‐induced downregulation of miR‐758‐3p—as part of a lncRNA EMS/miR‐758‐3p/WTAP axis—contributes to chemoresistance."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": " In glioblastoma, miR‐758‐5p has been implicated in tumor regulation via suppression of ZBTB20"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "8"}]}, {"type": "t", "text": ", while in breast cancer, competitive binding of the circular RNA hsa_circ_0069094 to miR‐758‐3p leads to de‐repression of oncogenes such as DCUN1D1, thereby promoting proliferation and invasion."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "9"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nCollectively, these findings underscore the context‐dependent versatility of miR‐758, which modulates key molecular targets across diverse biological systems—from regulating cholesterol metabolism and osteogenic differentiation to suppressing tumor growth and metastasis. Such multifunctionality not only highlights miR‐758’s potential as a biomarker for varied disease states but also suggests that therapeutic strategies aimed at restoring or modulating its expression may benefit conditions ranging from atherosclerosis to multiple malignancies.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Bi-Rong Li, Lin-Qin Xia, Jing Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "miR-758-5p regulates cholesterol uptake via targeting the CD36 3'UTR."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2017.09.150"}], "href": "https://doi.org/10.1016/j.bbrc.2017.09.150"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28965954"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28965954"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Wei Peng, Wei Deng, Jing Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Long noncoding RNA ANCR suppresses bone formation of periodontal ligament stem cells via sponging miRNA-758."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2018.06.081"}], "href": "https://doi.org/10.1016/j.bbrc.2018.06.081"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29913147"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29913147"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Dan Jiang, William C Cho, Zhenhao Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-758-3p suppresses proliferation, migration and invasion of hepatocellular carcinoma cells via targeting MDM2 and mTOR."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biomed Pharmacother (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biopha.2017.10.004"}], "href": "https://doi.org/10.1016/j.biopha.2017.10.004"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29032337"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29032337"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Sheng Wang, Ming Jiang "}, {"type": "b", "children": [{"type": "t", "text": "The long non-coding RNA-DANCR exerts oncogenic functions in non-small cell lung cancer via miR-758-3p."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biomed Pharmacother (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biopha.2018.03.053"}], "href": "https://doi.org/10.1016/j.biopha.2018.03.053"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29635134"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29635134"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "X M Li, Z Yu, M Huai, et al. "}, {"type": "b", "children": [{"type": "t", "text": "[miR-758-3p inhibits the proliferation and invasion of non-small cell lung cancer cells by targeting NUSAP1]."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Zhonghua Zhong Liu Za Zhi (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3760/cma.j.cn112152-20190727-00472"}], "href": "https://doi.org/10.3760/cma.j.cn112152-20190727-00472"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33472323"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33472323"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Jianping Chen, Zhenyu Xu, Changsheng Yu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-758-3p regulates papillary thyroid cancer cell proliferation and migration by targeting TAB1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Pharmazie (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1691/ph.2019.8933"}], "href": "https://doi.org/10.1691/ph.2019.8933"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30940308"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30940308"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Wenlong Xia, Libo Su, Jianwei Jiao "}, {"type": "b", "children": [{"type": "t", "text": "Cold-induced protein RBM3 orchestrates neurogenesis via modulating Yap mRNA stability in cold stress."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Biol (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1083/jcb.201801143"}], "href": "https://doi.org/10.1083/jcb.201801143"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30037926"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30037926"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Ji Liu, Jian Jiang, Xiaobo Hui, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mir-758-5p Suppresses Glioblastoma Proliferation, Migration and Invasion by Targeting ZBTB20."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Physiol Biochem (2018)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1159/000492545"}], "href": "https://doi.org/10.1159/000492545"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30099442"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30099442"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Jianguo Feng, Menghong Long, Xin Zhao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "RBM3 Accelerates Wound Healing of Skin in Diabetes through ERK1/2 Signaling."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Curr Mol Pharmacol (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.2174/0118761429260980231005105929"}], "href": "https://doi.org/10.2174/0118761429260980231005105929"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37982286"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37982286"}]}]}]}
Synonyms MIRN758, MIR-758, HSA-MIR-758
NCBI Gene ID 768212
API
Download Associations
Predicted Functions View MIR758's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR758's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR758's ARCHS4 Predicted Functions.

Functional Associations

MIR758 has 247 functional associations with biological entities spanning 5 categories (molecular profile, disease, phenotype or trait, functional term, phrase or reference, cell line, cell type or tissue, gene, protein or microRNA) extracted from 13 datasets.

Click the + buttons to view associations for MIR758 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 MIR758 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 MIR758 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
ChEA Transcription Factor Targets transcription factors binding the promoter of MIR758 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 MIR758 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.
CTD Gene-Disease Associations diseases associated with MIR758 gene/protein from the curated CTD Gene-Disease Associations dataset.
ENCODE Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at MIR758 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 MIR758 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of MIR758 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
GeneRIF Biological Term Annotations biological terms co-occuring with MIR758 gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
JASPAR Predicted Transcription Factor Targets transcription factors regulating expression of MIR758 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 MIR758 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 MIR758 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 MIR758 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.