| HGNC Family | Non-coding RNAs |
| Name | microRNA 8074 |
| 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": "\nMiRNA-8074 acts as a regulatory molecule in multiple myeloma by modulating key genes such as TP53, MYC, MAPK1, and KIAA, all of which are central to the disease’s pathogenesis. The study demonstrated that elevated expression levels of miRNA-8074 correlate with adverse clinical parameters, suggesting that it may influence crucial oncogenic pathways in MM."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFurthermore, high miRNA-8074 expression was significantly associated with reduced progression-free survival and overall survival in MM patients undergoing diverse treatment regimens, including thalidomide and bortezomib-based therapies. These findings highlight the potential value of miRNA-8074 not only as a molecule implicated in disease development but also as a prognostic biomarker that could improve risk stratification and guide treatment decisions in clinical settings."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Aneta Szudy-Szczyrek, Radosław Mlak, Michał Mielnik, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Circulating Serum MiRNA-8074 as a Novel Prognostic Biomarker for Multiple Myeloma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cells (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3390/cells11040752"}], "href": "https://doi.org/10.3390/cells11040752"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35203396"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35203396"}]}]}]}
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| Synonyms | HSA-MIR-8074 |
| NCBI Gene ID | 102465873 |
| API | |
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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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MIR8074 has 0 functional associations with biological entities spanning 0 categories () extracted from 0 datasets.
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If available, associations are ranked by standardized value
| Dataset | Summary |
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