MIR6875 Gene

HGNC Family Non-coding RNAs
Name microRNA 6875
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": "\nStudies in hepatocellular carcinoma have begun to explore the role of MIR6875, with one investigation specifically analyzing the miR‐6875-3p isoform. Although its precise function has yet to be fully elucidated, preliminary data suggest that miR‐6875-3p may be involved in the regulation of cellular mechanisms related to tumor occurrence, proliferation, invasion, and metastasis in this cancer type."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn the context of vaccine treatment for metastatic colorectal cancer, another line of research has associated elevated plasma levels of MIR6875 with a poorer prognosis. In this setting, increased expression of miR‐6875 correlates with reduced vaccine efficacy, positioning it as a potential non‐invasive biomarker to predict negative treatment outcomes."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFurther extending its clinical relevance, investigations into recurrent spontaneous abortion have identified that enhanced expression of the miR‐6875-5p isoform disrupts immune regulation by directly targeting the STAT3/E2-2 signaling pathway. This interaction impedes the differentiation of plasmacytoid dendritic cells, a process critical for successful fetal–maternal immunotolerance, thereby suggesting that aberrant MIR6875 levels may contribute to the pathogenesis of spontaneous abortion."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Yingjun Xie, Jian Du, Zefeng Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-6875-3p promotes the proliferation, invasion and metastasis of hepatocellular carcinoma via BTG2/FAK/Akt 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/s13046-018-1020-z"}], "href": "https://doi.org/10.1186/s13046-018-1020-z"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30621734"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30621734"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Taiki Kijima, Shoichi Hazama, Ryouichi Tsunedomi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MicroRNA-6826 and -6875 in plasma are valuable non‑invasive biomarkers that predict the efficacy of vaccine treatment against metastatic colorectal cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncol Rep (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3892/or.2016.5267"}], "href": "https://doi.org/10.3892/or.2016.5267"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27878288"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27878288"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Xiao-Xiao Zhu, Xun-Qiang Yin, Guo-Zhen Hei, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Increased miR-6875-5p inhibits plasmacytoid dendritic cell differentiation via the STAT3/E2-2 pathway in recurrent spontaneous abortion."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Hum Reprod (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1093/molehr/gaab044"}], "href": "https://doi.org/10.1093/molehr/gaab044"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34240166"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34240166"}]}]}]}
Synonyms HSA-MIR-6875
NCBI Gene ID 102466755
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Predicted Functions View MIR6875's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR6875's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR6875's ARCHS4 Predicted Functions.

Functional Associations

MIR6875 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.

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Dataset Summary