MIR3174 Gene

HGNC Family Non-coding RNAs
Name microRNA 3174
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": "\nMicroRNAs have emerged as key regulators of tumorigenesis with context‐dependent functions. Several studies implicate miR-3174 as a potential tumor promoter in multiple malignancies. In hepatocellular carcinoma, for instance, miR-3174 is suggested to contribute to oncogenesis, and in rectal cancer, although its physiological function remains unclear, its overall profile hints at a tumor‐promoting role. In addition, a study in endometrial cancer focused primarily on LINC00958, with no direct evidence implicating miR-3174, highlighting the need for further investigation in this tumor type."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "3"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn contrast to its putative oncogenic role in some cancers, emerging evidence in glioblastoma demonstrates a tumor-suppressive function for miR-3174. Experimental data reveal that miR-3174 is downregulated in glioblastoma cells and tissues relative to normal brain tissue. Restoration of miR-3174 expression markedly inhibited cell proliferation, invasion, and neurosphere formation via simultaneous downregulation of several tumor-promoting genes such as CD44, MDM2, RHOA, PLAU, and CDK6. These findings suggest that, in the context of glioblastoma, miR-3174 acts as an important inhibitor of tumor growth and could potentially be developed as a therapeutic agent."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nStudies in breast cancer further underscore the complex and context-specific role of miR-3174. In breast cancer cells, treatment with cisatracurium significantly reduced miR-3174 expression, which was associated with inhibition of cell proliferation, migration, and invasion. Downregulation of miR-3174 led to increased expression of tumor-suppressive factors such as p21 and a concurrent decrease in pro-proliferative markers like Cyclin D1, MMP-2, and MMP-9. Conversely, re-establishing miR-3174 levels reversed these effects, indicating its function as a tumor promoter in breast cancer."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Qingyuan Wang, Xiao Yang, Xiao Zhou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-3174 promotes proliferation and inhibits apoptosis by targeting FOXO1 in hepatocellular carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2020.03.152"}], "href": "https://doi.org/10.1016/j.bbrc.2020.03.152"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32279994"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32279994"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "D-L Zhang, N Yang "}, {"type": "b", "children": [{"type": "t", "text": "MiR-3174 functions as an oncogene in rectal cancer by targeting PCBD2."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur Rev Med Pharmacol Sci (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.26355/eurrev_201903_17388"}], "href": "https://doi.org/10.26355/eurrev_201903_17388"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30964167"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30964167"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Q-Y Li, J-Q Shen, J-H Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "LINC00958/miR-3174/PHF6 axis is responsible for triggering proliferation, migration and invasion of endometrial cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur Rev Med Pharmacol Sci (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.26355/eurrev_202111_27233"}], "href": "https://doi.org/10.26355/eurrev_202111_27233"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34859848"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34859848"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Farina Hanif, Ying Zhang, Collin Dube, et al. "}, {"type": "b", "children": [{"type": "t", "text": "miR-3174 Is a New Tumor Suppressor MicroRNA That Inhibits Several Tumor-Promoting Genes in Glioblastoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Mol Sci (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3390/ijms24119326"}], "href": "https://doi.org/10.3390/ijms24119326"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37298284"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37298284"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Xiaozhong Yang, Wenxia Ma "}, {"type": "b", "children": [{"type": "t", "text": "Cisatracurium inhibits the proliferation, migration and invasion of breast cancer cells by regulating the expression of miR-3174."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Mol Biol (Noisy-le-grand) (2020)"}]}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33040777"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33040777"}]}]}]}
NCBI Gene ID 100422841
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Predicted Functions View MIR3174's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR3174's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR3174's ARCHS4 Predicted Functions.

Functional Associations

MIR3174 has 108 functional associations with biological entities spanning 1 categories (cell line, cell type or tissue) extracted from 2 datasets.

Click the + buttons to view associations for MIR3174 from the datasets below.

If available, associations are ranked by standardized value

Dataset Summary
GTEx Tissue Gene Expression Profiles tissues with high or low expression of MIR3174 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.
Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles cell lines with high or low copy number of MIR3174 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.