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Serine/arginine-rich splicing factors: the bridge linking alternative splicing and cancer

The serine/arginine-rich splicing factors (SRs) belong to the serine arginine-rich protein family, which plays an extremely important role in the splicing process of precursor RNA. The SRs recognize the splicing elements on precursor RNA, then recruit and assemble spliceosome to promote or inhibit t...

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Detalles Bibliográficos
Autores principales: Zheng, Xiang, Peng, Qiu, Wang, Lujuan, Zhang, Xuemei, Huang, Lili, Wang, Jia, Qin, Zailong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378643/
https://www.ncbi.nlm.nih.gov/pubmed/32760211
http://dx.doi.org/10.7150/ijbs.46751
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author Zheng, Xiang
Peng, Qiu
Wang, Lujuan
Zhang, Xuemei
Huang, Lili
Wang, Jia
Qin, Zailong
author_facet Zheng, Xiang
Peng, Qiu
Wang, Lujuan
Zhang, Xuemei
Huang, Lili
Wang, Jia
Qin, Zailong
author_sort Zheng, Xiang
collection PubMed
description The serine/arginine-rich splicing factors (SRs) belong to the serine arginine-rich protein family, which plays an extremely important role in the splicing process of precursor RNA. The SRs recognize the splicing elements on precursor RNA, then recruit and assemble spliceosome to promote or inhibit the occurrence of splicing events. In tumors, aberrant expression of SRs causes abnormal splicing of RNA, contributing to proliferation, migration and apoptosis resistance of tumor cells. Here, we reviewed the vital role of SRs in various tumors and discussed the promise of analyzing mRNA alternative splicing events in tumor. Further, we highlight the challenges and discussed the perspectives for the identification of new potential targets for cancer therapy via SRs family members.
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spelling pubmed-73786432020-08-04 Serine/arginine-rich splicing factors: the bridge linking alternative splicing and cancer Zheng, Xiang Peng, Qiu Wang, Lujuan Zhang, Xuemei Huang, Lili Wang, Jia Qin, Zailong Int J Biol Sci Review The serine/arginine-rich splicing factors (SRs) belong to the serine arginine-rich protein family, which plays an extremely important role in the splicing process of precursor RNA. The SRs recognize the splicing elements on precursor RNA, then recruit and assemble spliceosome to promote or inhibit the occurrence of splicing events. In tumors, aberrant expression of SRs causes abnormal splicing of RNA, contributing to proliferation, migration and apoptosis resistance of tumor cells. Here, we reviewed the vital role of SRs in various tumors and discussed the promise of analyzing mRNA alternative splicing events in tumor. Further, we highlight the challenges and discussed the perspectives for the identification of new potential targets for cancer therapy via SRs family members. Ivyspring International Publisher 2020-07-06 /pmc/articles/PMC7378643/ /pubmed/32760211 http://dx.doi.org/10.7150/ijbs.46751 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Zheng, Xiang
Peng, Qiu
Wang, Lujuan
Zhang, Xuemei
Huang, Lili
Wang, Jia
Qin, Zailong
Serine/arginine-rich splicing factors: the bridge linking alternative splicing and cancer
title Serine/arginine-rich splicing factors: the bridge linking alternative splicing and cancer
title_full Serine/arginine-rich splicing factors: the bridge linking alternative splicing and cancer
title_fullStr Serine/arginine-rich splicing factors: the bridge linking alternative splicing and cancer
title_full_unstemmed Serine/arginine-rich splicing factors: the bridge linking alternative splicing and cancer
title_short Serine/arginine-rich splicing factors: the bridge linking alternative splicing and cancer
title_sort serine/arginine-rich splicing factors: the bridge linking alternative splicing and cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378643/
https://www.ncbi.nlm.nih.gov/pubmed/32760211
http://dx.doi.org/10.7150/ijbs.46751
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