MIR6809 Gene

HGNC Family Non-coding RNAs
Name microRNA 6809
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 underscored the importance of noncoding RNAs and RNA‐binding proteins in maintaining cellular homeostasis and regulating tumorigenesis. For example, luteolin, a naturally occurring flavonoid, has been shown to induce apoptosis in hepatocellular carcinoma cells without fully elucidating its downstream molecular mechanisms."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " In parallel, investigations into zinc finger proteins such as ZFP207 have revealed critical roles in ensuring proper spindle assembly and chromosome alignment during meiosis"}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": ", as well as in orchestrating alternative splicing networks to preserve embryonic stem cell identity."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn the context of acute myeloid leukemia, miR‐6809 emerges as a pivotal player in cell cycle regulation. Specifically, one study has demonstrated that the long noncoding RNA LINC00675 exerts oncogenic effects by binding to miR‐6809, thereby preventing it from suppressing the expression of CDK6—a key regulator of cell proliferation. The sequestration of miR‐6809 by LINC00675 leads to increased CDK6 levels, promoting malignant cell growth and survival, while also correlating with elevated expression of immune-checkpoint genes. This interaction not only enhances AML malignancy by reducing apoptosis but also suggests that targeting the LINC00675/miR‐6809/CDK6 axis could offer new avenues for therapeutic intervention."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nCollectively, these findings position miR‐6809 as a tumor‐suppressive microRNA whose regulatory activity—primarily through the inhibition of CDK6 expression—is compromised in AML due to its sponging by LINC00675. While other studies have shed light on the diverse regulatory mechanisms influencing apoptosis, meiotic progression, and stem cell maintenance, the distinct role of miR‐6809 in modulating cell cycle progression and oncogenic signaling in AML highlights its potential as a strategic target for future therapeutic developments.\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Pei-Wei Yang, Zheng-Yu Lu, Qing Pan, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MicroRNA-6809-5p mediates luteolin-induced anticancer effects against hepatoma by targeting flotillin 1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Phytomedicine (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.phymed.2018.10.027"}], "href": "https://doi.org/10.1016/j.phymed.2018.10.027"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30668319"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30668319"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Xiao Xin Dai, Hao Xiong, Mianqun Zhang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Zfp207 is a Bub3 binding protein regulating meiotic chromosome alignment in mouse oocytes."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Oncotarget (2016)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.18632/oncotarget.9310"}], "href": "https://doi.org/10.18632/oncotarget.9310"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "27177335"}], "href": "https://pubmed.ncbi.nlm.nih.gov/27177335"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Sandhya Malla, Devi Prasad Bhattarai, Paula Groza, et al. "}, {"type": "b", "children": [{"type": "t", "text": "ZFP207 sustains pluripotency by coordinating OCT4 stability, alternative splicing and RNA export."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "EMBO Rep (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.15252/embr.202153191"}], "href": "https://doi.org/10.15252/embr.202153191"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35037361"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35037361"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Xinyi Long, Huinan Jiang, Zhuogang Liu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Long noncoding RNA LINC00675 drives malignancy in acute myeloid leukemia via the miR-6809 -CDK6 axis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Pathol Res Pract (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.prp.2024.155221"}], "href": "https://doi.org/10.1016/j.prp.2024.155221"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "38422911"}], "href": "https://pubmed.ncbi.nlm.nih.gov/38422911"}]}]}]}
Synonyms HSA-MIR-6809
NCBI Gene ID 102465485
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Predicted Functions View MIR6809's ARCHS4 Predicted Functions.
Co-expressed Genes View MIR6809's ARCHS4 Predicted Functions.
Expression in Tissues and Cell Lines View MIR6809's ARCHS4 Predicted Functions.

Functional Associations

MIR6809 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.

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Dataset Summary