| HGNC Family | Non-coding RNAs |
| Name | microRNA 6756 |
| 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 evidence has revealed that hsa_miR-6756-5p functions as a pivotal post‐transcriptional regulator in penile mesenchymal cell development by modulating androgen receptor (AR) signaling. In normal physiology, the circular RNA hsa_circ_0000417 acts as a competing endogenous RNA (ceRNA), sequestering hsa_miR-6756-5p and thereby maintaining appropriate AR levels and ensuring the proper balance of cell proliferation and apoptosis via pathways such as PI3K/AKT. However, in hypospadias—a congenital malformation resulting from urethral closure failure—downregulation of hsa_circ_0000417 likely leads to increased availability of hsa_miR-6756-5p. This excess microRNA is then posited to dysregulate AR expression, ultimately perturbing downstream signaling cascades that control penile mesenchymal cell survival and proliferation."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Junqiang Huang, Cheng Su, Pingan Lu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "hsa_circ_0000417 downregulation suppresses androgen receptor expression and apoptotic signals in human foreskin fibroblasts via sponging miR-6756-5p."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Rep (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s11033-023-08628-6"}], "href": "https://doi.org/10.1007/s11033-023-08628-6"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37389702"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37389702"}]}]}]}
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| Synonyms | HSA-MIR-6756 |
| NCBI Gene ID | 102465453 |
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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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MIR6756 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
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| Dataset | Summary |
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