| HGNC Family | Non-coding RNAs |
| Name | microRNA 6511b-2 |
| 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": "\nColorectal cancer patients with distal metastases face a poor prognosis, and nearly 95% of metastatic cases exhibit DNA mismatch repair proficiency (pMMR). In this context, recent findings have shown that miR-6511b-5p—a form of MIR6511B2—is downregulated in pMMR colorectal cancer, hinting at its potential involvement in the regulatory networks that control metastatic progression."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nThough the precise mechanism by which miR-6511b-5p influences metastasis remains unclear, its decreased expression in pMMR tumors suggests that MIR6511B2 could normally act to suppress pathways that promote tumor dissemination. Identifying the molecular targets and signaling cascades affected by miR-6511b-5p may provide valuable insights into novel therapeutic strategies for managing metastatic colorectal cancer."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "JinMing Sun, Ling Ye, Yuan Shi, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-6511b-5p suppresses metastasis of pMMR colorectal cancer through methylation of CD44 by directly targeting BRG1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Clin Transl Oncol (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s12094-022-02845-4"}], "href": "https://doi.org/10.1007/s12094-022-02845-4"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35590122"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35590122"}]}]}]}
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| Synonyms | MIR6511B-2, HSA-MIR-6511B-2 |
| NCBI Gene ID | 102465985 |
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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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MIR6511B2 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
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| Dataset | Summary |
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