MIR675 Gene

HGNC Family Non-coding RNAs
Name microRNA 675
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‐675, a microRNA processed from the first exon of the imprinted long noncoding RNA H19, has emerged as a critical regulatory molecule in cancer. In colorectal cancer, for example, miR‐675 is up‐regulated and promotes tumorigenesis by directly targeting and downregulating the tumor suppressor retinoblastoma protein (RB)."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " Conversely, in prostate cancer, diminished H19/miR‐675 levels have been associated with malignant progression, with restoration of miR‐675 levels reducing cell migration through the repression of transforming growth factor β–induced protein (TGFBI)."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": " Elevated levels of miR‐675 have also been documented in gliomas, where it promotes tumor invasion by modulating Cadherin 13 expression"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": ", in gastric cancer where miR‐675 targets the tumor suppressor RUNX1 to enhance cell proliferation"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": ", and in aggressive breast cancers, where its up‐regulation drives an invasive phenotype via downregulation of ubiquitin ligases that normally restrict receptor tyrosine kinase signaling."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": " In bladder cancer, miR‐675 overexpression contributes to abnormal cell proliferation by interfering with p53 activation and perturbing apoptotic regulators."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "6"}]}, {"type": "t", "text": " Similar oncogenic roles have been observed in non–small cell lung and head and neck cancers"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "7"}]}, {"type": "t", "text": ", and additional studies in gastric and liver cancers have further implicated miR‐675 in promoting malignant phenotypes by modulating key signaling pathways such as AKT/mTOR and by affecting cell cycle regulators."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "9", "end_ref": "12"}]}, {"type": "t", "text": " Furthermore, in glioma a direct targeting of the retinoblastoma gene (RB1) by miR‐675 was demonstrated to enhance proliferative and invasive capacities"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "13"}]}, {"type": "t", "text": ", while exosomal transfer of miR‐675 has been linked to the metastatic behavior of osteosarcoma."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "14"}]}, {"type": "t", "text": " In plasma from breast cancer patients, correlations between circulating H19 and miR‐675 further underscore its potential as a diagnostic marker, and the identification of competing endogenous RNAs (such as circKDM4B) that sponge miR‐675 highlights its significance in modulating tumor progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "15"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nMechanistically, miR‐675 exerts its regulatory effects by targeting a spectrum of molecules that modulate key signaling networks. In gastric cancer, beyond RUNX1, miR‐675 has been shown to facilitate malignant behavior by enhancing the AKT/mTOR pathway."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "17"}]}, {"type": "t", "text": " It can also destabilize epithelial integrity by directly binding the 3′‐untranslated regions of tight junction and adherens junction proteins—such as ZO‐1 and E‐cadherin—thereby compromising intestinal barrier function."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "18"}]}, {"type": "t", "text": " In the context of cell fate and differentiation, miR‐675 targets histone deacetylases 4–6 to modulate adipogenic commitment of bone marrow mesenchymal stem cells"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "19"}]}, {"type": "t", "text": ", and it directly binds to the 3′‐UTR of MITF in keratinocytes to influence melanogenesis."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "20"}]}, {"type": "t", "text": " Moreover, alterations in p53 signaling observed in liver cancer and hepatocyte injury have been linked to elevated miR‐675 levels"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "21"}]}, {"type": "t", "text": ", while in HBV‐associated liver injury and diabetic nephropathy the H19/miR‐675 axis modulates PPARα and the vitamin D receptor/EGR1 pathway to impact cell survival and energy metabolism."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "22"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its role in tumorigenesis, miR‐675 is integral to several physiological and developmental processes. 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Synonyms MIRN675, HSA-MIR-675
NCBI Gene ID 100033819
API
Download Associations
Predicted Functions View MIR675's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR675's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR675's ARCHS4 Predicted Functions.

Functional Associations

MIR675 has 740 functional associations with biological entities spanning 5 categories (molecular profile, functional term, phrase or reference, chemical, cell line, cell type or tissue, gene, protein or microRNA) extracted from 14 datasets.

Click the + buttons to view associations for MIR675 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 MIR675 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 MIR675 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
ChEA Transcription Factor Targets transcription factors binding the promoter of MIR675 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset.
ENCODE Histone Modification Site Profiles histone modification site profiles with high histone modification abundance at MIR675 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 MIR675 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
ENCODE Transcription Factor Targets transcription factors binding the promoter of MIR675 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
GeneRIF Biological Term Annotations biological terms co-occuring with MIR675 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 MIR675 from the GeneSigDB Published Gene Signatures dataset.
GEO Signatures of Differentially Expressed Genes for Small Molecules small molecule perturbations changing expression of MIR675 gene from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset.
GEO Signatures of Differentially Expressed Genes for Transcription Factor Perturbations transcription factor perturbations changing expression of MIR675 gene from the GEO Signatures of Differentially Expressed Genes for Transcription Factor Perturbations dataset.
JASPAR Predicted Transcription Factor Targets transcription factors regulating expression of MIR675 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 MIR675 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 MIR675 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 MIR675 gene from the Roadmap Epigenomics Histone Modification Site Profiles dataset.