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Genome-Wide Analyses of Prognostic and Therapeutic Alternative Splicing Signatures in Bladder Urothelial Carcinoma

Overview
Journal Front Oncol
Specialty Oncology
Date 2021 Apr 12
PMID 33842332
Citations 3
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Abstract

Background: Alternative splicing (AS) is an indispensable post-transcriptional modification applied during the maturation of mRNA, and AS defects have been associated with many cancers. This study was designed to thoroughly analyze AS events in bladder urothelial carcinoma (BLCA) at the genome-wide level.

Methods: We adopted a gap analysis to screen for significant differential AS events (DASEs) associated with BLCA. DASEs with prognostic value for OS and the disease-free interval (DFI) were identified by Cox analysis. In addition, a differential AS network and AS clusters were identified using unsupervised cluster analysis. We examined differences in the sensitivity to chemotherapy and immunotherapy between BLCA patients with high and low overall survival (OS) risk.

Results: An extensive number of DASEs (296) were found to be clinically relevant in BLCA. A prognosis model was established based prognostic value of OS and DFI. CUGBP elav-like family member 2 (CELF2) was identified as a hub splicing factor for AS networks. We also identified AS clusters associated with OS using unsupervised cluster analysis, and we predicted that the effects of cisplatin and gemcitabine chemotherapy would be different between high- and low-risk groups based on OS prognosis.

Conclusion: We completed a comprehensive analysis of AS events in BLCA at the genome-wide level. The present findings revealed that DASEs and splicing factors tended to impact BLCA patient survival and sensitivity to chemotherapy drugs, which may provide novel prospects for BLCA therapies.

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References
1.
Cao R, Zhang J, Jiang L, Wang Y, Ren X, Cheng B . Comprehensive Analysis of Prognostic Alternative Splicing Signatures in Oral Squamous Cell Carcinoma. Front Oncol. 2020; 10:1740. PMC: 7485395. DOI: 10.3389/fonc.2020.01740. View

2.
Chatrikhi R, Mallory M, Gazzara M, Agosto L, Zhu W, Litterman A . RNA Binding Protein CELF2 Regulates Signal-Induced Alternative Polyadenylation by Competing with Enhancers of the Polyadenylation Machinery. Cell Rep. 2019; 28(11):2795-2806.e3. PMC: 6752737. DOI: 10.1016/j.celrep.2019.08.022. View

3.
Sznajder L, Scotti M, Shin J, Taylor K, Ivankovic F, Nutter C . Loss of MBNL1 induces RNA misprocessing in the thymus and peripheral blood. Nat Commun. 2020; 11(1):2022. PMC: 7181699. DOI: 10.1038/s41467-020-15962-x. View

4.
Piva F, Giulietti M, Burini A, Principato G . SpliceAid 2: a database of human splicing factors expression data and RNA target motifs. Hum Mutat. 2011; 33(1):81-5. DOI: 10.1002/humu.21609. View

5.
DasGupta T, Ladd A . The importance of CELF control: molecular and biological roles of the CUG-BP, Elav-like family of RNA-binding proteins. Wiley Interdiscip Rev RNA. 2011; 3(1):104-21. PMC: 3243963. DOI: 10.1002/wrna.107. View