| HGNC Family | Non-coding RNAs |
| Name | microRNA 513b |
| 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": "\nMicroRNA‐513b‐5p has emerged as a critical regulator in several disease contexts, notably in cancer. In non‐small cell lung cancer (NSCLC), its expression is significantly downregulated, and restoration of miR‐513b‐5p levels suppresses cell proliferation, migration, and invasion while promoting apoptosis by directly targeting HMGB3, thereby acting as a tumor suppressor (see."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": " In hepatocellular carcinoma (HCC), miR‐513b‐5p similarly restrains malignant progression by inhibiting autophagy through downregulation of PIK3R3, leading to reduced LC3‐II and beclin1 levels and decreased cell growth and metastatic behavior."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "2"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn vascular smooth muscle cells, miR‐513b‐5p modulates extracellular remodeling by suppressing the expression of collagen type I chains (COL1A1 and COL1A2) and affecting cell death pathways—including the RIP1‐RIP3‐MLKL cascade and matrix metalloproteinase signaling—which may contribute to the formation and rupture of intracranial aneurysms."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "3"}]}, {"type": "t", "text": " Conversely, in the context of breast cancer, the long noncoding RNA LINC00675 acts as a competing endogenous RNA that sequesters miR‐513b‐5p; its downregulation leads to increased miR‐513b‐5p activity, and this axis appears to promote malignant features, suggesting that miR‐513b‐5p might have oncogenic properties in this tissue type."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "4"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nMoreover, in lung cancer models using A549 cells, treatment with Solanum lyratum polysaccharide results in upregulation of miR‐513b‐5p, which correlates with reduced cell proliferation, migration, and invasion, and with enhanced apoptosis. These findings underscore the therapeutic potential of modulating miR‐513b‐5p levels to harness its tumor‐suppressive effects in lung cancer."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "5"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Jiying Wang, Zhaoying Sheng, Yong Cai "}, {"type": "b", "children": [{"type": "t", "text": "Effects of microRNA-513b on cell proliferation, apoptosis, invasion, and migration by targeting HMGB3 through regulation of mTOR signaling pathway in non-small-cell lung cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Physiol (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcp.27921"}], "href": "https://doi.org/10.1002/jcp.27921"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30623409"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30623409"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Wei Jin, Yilei Liang, Shuyou Li, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MiR-513b-5p represses autophagy during the malignant progression of hepatocellular carcinoma by targeting PIK3R3."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Aging (Albany NY) (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.18632/aging.203135"}], "href": "https://doi.org/10.18632/aging.203135"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34120890"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34120890"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Zheng Zheng, Yan Chen, Yinzhou Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "MicroRNA-513b-5p targets COL1A1 and COL1A2 associated with the formation and rupture of intracranial aneurysm."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41598-021-94116-5"}], "href": "https://doi.org/10.1038/s41598-021-94116-5"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34290266"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34290266"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Shenglan Fan, Liping Wang "}, {"type": "b", "children": [{"type": "t", "text": "N"}, {"type": "a", "children": [{"type": "t", "text": "sup"}], "href": "sup"}, {"type": "t", "text": "6"}, {"type": "a", "children": [{"type": "t", "text": "/sup"}], "href": "/sup"}, {"type": "t", "text": "-Methyladenosine-regulated LINC00675 suppress the proliferation, migration and invasion of breast cancer cells via inhibiting miR-513b-5p."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Bioengineered (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1080/21655979.2021.2001905"}], "href": "https://doi.org/10.1080/21655979.2021.2001905"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "34738869"}], "href": "https://pubmed.ncbi.nlm.nih.gov/34738869"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Yuyu Feng, Wei Wang, Conghui Liu "}, {"type": "b", "children": [{"type": "t", "text": "Effect of Solanum lyratum Polysaccharide on Malignant Behaviors of Lung Cancer Cells by Regulating the Circ_UHRF1/miR-513b-5p Axis."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Cell Mol Biol (Noisy-le-grand) (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.14715/cmb/2021.67.6.26"}], "href": "https://doi.org/10.14715/cmb/2021.67.6.26"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35818196"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35818196"}]}]}]}
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| Synonyms | MIRN513B |
| NCBI Gene ID | 100313822 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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MIR513B has 80 functional associations with biological entities spanning 1 categories (cell line, cell type or tissue) extracted from 1 datasets.
Click the + buttons to view associations for MIR513B from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MIR513B gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |