| HGNC Family | Non-coding RNAs |
| Name | microRNA 6869 |
| 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 elucidated a critical role for miR‐6869‐5p in regulating cellular proliferation and invasion in cancer. In glioma, miR‐6869‐5p is significantly downregulated, a change that is associated with elevated levels of its target, PGK1. This loss of miR‐6869‐5p function facilitates increased tumor cell proliferation and invasiveness, and its diminished expression correlates with a poorer patient prognosis, highlighting its role as a tumor suppressor and promising prognostic marker."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "Disruptions in miR‐6869‐5p expression have also been implicated in the context of gestational diabetes mellitus, where its reduced levels in placenta‐derived mononuclear macrophages contribute to an imbalanced placental microenvironment. Specifically, miR‐6869‐5p directly targets PTPRO, and its downregulation promotes abnormal macrophage proliferation and a skewing away from the anti‐inflammatory M2 phenotype. This shift fosters a pro‐inflammatory milieu that may underlie adverse placental and immune outcomes in gestational diabetes mellitus."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Fakai Wang, Huanjun Zhang, Bing Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "miR-6869-5p Inhibits Glioma Cell Proliferation and Invasion via Targeting PGK1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mediators Inflamm (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1155/2020/9752372"}], "href": "https://doi.org/10.1155/2020/9752372"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32565733"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32565733"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Pingping Wang, Zhenzhi Ma, Zengyan Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-6869-5p Induces M2 Polarization by Regulating PTPRO in Gestational Diabetes Mellitus."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mediators Inflamm (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1155/2021/6696636"}], "href": "https://doi.org/10.1155/2021/6696636"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34007244"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34007244"}]}]}]}
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| Synonyms | HSA-MIR-6869 |
| NCBI Gene ID | 102465524 |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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MIR6869 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
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| Dataset | Summary |
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