| Name | MYO16 antisense RNA 1 |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nRecent studies have highlighted the pivotal role of long noncoding RNAs (lncRNAs) acting as competitive endogenous RNAs (ceRNAs) in cancer development. In muscle-invasive bladder cancer (MIBC), RNA sequence profiling led to the construction of a ceRNA network comprising aberrantly expressed mRNAs, lncRNAs, and miRNAs, among which MYO16‐AS1 was identified. This network provided insights into the molecular mechanisms underlying tumor progression in MIBC."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nWithin this network, MYO16‐AS1 emerged as one of eight lncRNAs that form a prognostic signature for MIBC. Its elevated expression was statistically correlated with worsened overall survival in patients, suggesting that MYO16‐AS1 plays a significant oncogenic role."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nFurthermore, experimental assays demonstrated that overexpression of MYO16‐AS1 enhanced UMUC2 cell migration and invasion, confirming its functional contribution to bladder cancer progression. These findings propose that MYO16‐AS1 may serve as both a biomarker for prognostic prediction and a potential therapeutic target in MIBC."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "1"}]}, {"type": "t", "text": ""}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Danyang Shen, Youyun Zhang, Qiming Zheng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A Competing Endogenous RNA Network and an 8-lncRNA Prognostic Signature Identify "}, {"type": "a", "children": [{"type": "t", "text": "i"}], "href": "i"}, {"type": "t", "text": "MYO16-AS1"}, {"type": "a", "children": [{"type": "t", "text": "/i"}], "href": "/i"}, {"type": "t", "text": " as an Oncogenic lncRNA in Bladder Cancer."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "DNA Cell Biol (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1089/dna.2020.6014"}], "href": "https://doi.org/10.1089/dna.2020.6014"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33270518"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33270518"}]}]}]}
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| NCBI Gene ID | 100885782 |
| 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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MYO16-AS1 has 166 functional associations with biological entities spanning 2 categories (cell line, cell type or tissue, gene, protein or microRNA) extracted from 5 datasets.
Click the + buttons to view associations for MYO16-AS1 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CCLE Cell Line Gene CNV Profiles | cell lines with high or low copy number of MYO16-AS1 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset. | |
| COSMIC Cell Line Gene CNV Profiles | cell lines with high or low copy number of MYO16-AS1 gene relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset. | |
| GTEx Tissue Gene Expression Profiles | tissues with high or low expression of MYO16-AS1 gene relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. | |
| Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles | cell lines with high or low copy number of MYO16-AS1 gene relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset. | |
| MotifMap Predicted Transcription Factor Targets | transcription factors regulating expression of MYO16-AS1 gene predicted using known transcription factor binding site motifs from the MotifMap Predicted Transcription Factor Targets dataset. | |