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1000 Titel
  • Long noncoding RNA MIR31HG and its splice variants regulate proliferation and migration: prognostic implications for muscle invasive bladder cancer
1000 Autor/in
  1. Wu, Sheng |
  2. Nitschke, Katja |
  3. Worst, Thomas Stefan |
  4. Fierek, Alexander |
  5. Weis, Cleo-Aron |
  6. Eckstein, Markus |
  7. Porubsky, Stefan |
  8. Kriegmair, Maximilian |
  9. Erben, Philipp |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-12-17
1000 Erschienen in
1000 Quellenangabe
  • 39(1):288
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13046-020-01795-5 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7745499/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Growing evidence supports the pivotal role of long non-coding RNAs (lncRNAs) in the regulation of cancer development and progression. Their expression patterns and biological function in muscle invasive bladder cancer (MIBC) remain elusive.!##!Methods!#!Transcript levels of lncRNA miR-31 host gene (MIR31HG) and its splice variants were measured in our MIBC cohort (n = 102) by qRT-PCR, and validated in silico by the TCGA cohort (n = 370). Kaplan-Meier and multiple Cox regression analysis were conducted to evaluate the survival significance of MIR31HG and its splice variants. Functional experiments were performed to examine the proliferation and migration abilities of MIR31HG and its splice variants by knockdown approaches.!##!Results!#!In this study, a decreased expression of MIR31HG was found in bladder cancer cells and tissues, except in the basal subtype. Survival analysis showed that high expression of MIR31HG was associated with poor overall survival (OS) and disease-free survival (DFS) in patients with MIBC of basal subtype. Two splice variants of MIR31HG lacking exon 1 (MIR31HGΔE1) and exon 3 (MIR31HGΔE3) were identified to have specific expression patterns in different molecular subtypes of our MIBC cohort. MIR31HGΔE3 was highly expressed in basal subtype tumors. A high expression of MIR31HGΔE1 and MIR31HGΔE3 was associated with worse OS and DFS in our cohort. In vitro experiments revealed that knockdown of MIR31HG inhibits cell proliferation, colony formation, and migration in bladder cancer. Cell proliferation and migration assays after knockdown of splice variants of MIR31HG showed corresponding roles for the full-length transcript.!##!Conclusions!#!Our study demonstrates that MIR31HG and its splice variants could serve as biomarkers for the classification and prognosis prediction of patients with MIBC.
1000 Sacherschließung
lokal Gene Expression Regulation, Neoplastic [MeSH]
lokal Aged, 80 and over [MeSH]
lokal Aged [MeSH]
lokal Cell Movement [MeSH]
lokal Muscle Neoplasms/pathology [MeSH]
lokal RNA, Long Noncoding/genetics [MeSH]
lokal Muscle Neoplasms/genetics [MeSH]
lokal Apoptosis [MeSH]
lokal Biomarker
lokal Tumor Cells, Cultured [MeSH]
lokal RNA Splicing [MeSH]
lokal Male [MeSH]
lokal Urinary Bladder Neoplasms/genetics [MeSH]
lokal Muscle Neoplasms/metabolism [MeSH]
lokal
lokal Female [MeSH]
lokal Cell Proliferation [MeSH]
lokal Molecular subtype
lokal Adult [MeSH]
lokal Urinary Bladder Neoplasms/metabolism [MeSH]
lokal Humans [MeSH]
lokal Retrospective Studies [MeSH]
lokal Middle Aged [MeSH]
lokal Urinary Bladder Neoplasms/pathology [MeSH]
lokal Neoplasm Invasiveness [MeSH]
lokal LncRNA
lokal Survival Rate [MeSH]
lokal Muscle invasive bladder cancer
lokal Biomarkers, Tumor/metabolism [MeSH]
lokal Research
lokal Biomarkers, Tumor/genetics [MeSH]
lokal Prognosis [MeSH]
1000 Liste der Beteiligten
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