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Comprehensive analysis of alternative polyadenylation regulators concerning CD276 and immune infiltration in bladder cancer

Alternative polyadenylation (APA) is emerging as a crucial regulatory mechanism in bladder cancer (BC), while it remains elusive whether APA influences the tumor immune microenvironment (TIME) in BC. We identified two distinct subtypes of BC by APA-related regulatory genes expression profiles. The t...

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Autores principales: Xiong, Ming, Li, Wencheng, Wang, Longwang, Chen, Liang, Chen, Zhaohui, Wei, Chengcheng, Zhang, Futian, Chen, Jiawei, Kazobinka, Gallina, Zhao, Jun, Hou, Teng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520876/
https://www.ncbi.nlm.nih.gov/pubmed/36175880
http://dx.doi.org/10.1186/s12885-022-10103-7
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author Xiong, Ming
Li, Wencheng
Wang, Longwang
Chen, Liang
Chen, Zhaohui
Wei, Chengcheng
Zhang, Futian
Chen, Jiawei
Kazobinka, Gallina
Zhao, Jun
Hou, Teng
author_facet Xiong, Ming
Li, Wencheng
Wang, Longwang
Chen, Liang
Chen, Zhaohui
Wei, Chengcheng
Zhang, Futian
Chen, Jiawei
Kazobinka, Gallina
Zhao, Jun
Hou, Teng
author_sort Xiong, Ming
collection PubMed
description Alternative polyadenylation (APA) is emerging as a crucial regulatory mechanism in bladder cancer (BC), while it remains elusive whether APA influences the tumor immune microenvironment (TIME) in BC. We identified two distinct subtypes of BC by APA-related regulatory genes expression profiles. The two subtypes have different pathological grades, prognostic outcomes, tumor immune infiltration characteristics, and pathway enrichment. Subsequently, CPSF3 was identified as a potential immune infiltration-related gene in BC. Highly expressed CPSF3 was positively correlated with unfavorable prognosis and high CD276 expression in BC. Moreover, we verified the expression of CPSF3 in BC tissues and cell lines by qRT-PCR. In conclusion, the study indicates that APA regulatory factors play an important role in immune infiltration of BC, and that CPSF3 was a potentially prognostic marker and immunotherapy target for BC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10103-7.
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spelling pubmed-95208762022-09-30 Comprehensive analysis of alternative polyadenylation regulators concerning CD276 and immune infiltration in bladder cancer Xiong, Ming Li, Wencheng Wang, Longwang Chen, Liang Chen, Zhaohui Wei, Chengcheng Zhang, Futian Chen, Jiawei Kazobinka, Gallina Zhao, Jun Hou, Teng BMC Cancer Research Alternative polyadenylation (APA) is emerging as a crucial regulatory mechanism in bladder cancer (BC), while it remains elusive whether APA influences the tumor immune microenvironment (TIME) in BC. We identified two distinct subtypes of BC by APA-related regulatory genes expression profiles. The two subtypes have different pathological grades, prognostic outcomes, tumor immune infiltration characteristics, and pathway enrichment. Subsequently, CPSF3 was identified as a potential immune infiltration-related gene in BC. Highly expressed CPSF3 was positively correlated with unfavorable prognosis and high CD276 expression in BC. Moreover, we verified the expression of CPSF3 in BC tissues and cell lines by qRT-PCR. In conclusion, the study indicates that APA regulatory factors play an important role in immune infiltration of BC, and that CPSF3 was a potentially prognostic marker and immunotherapy target for BC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10103-7. BioMed Central 2022-09-29 /pmc/articles/PMC9520876/ /pubmed/36175880 http://dx.doi.org/10.1186/s12885-022-10103-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Xiong, Ming
Li, Wencheng
Wang, Longwang
Chen, Liang
Chen, Zhaohui
Wei, Chengcheng
Zhang, Futian
Chen, Jiawei
Kazobinka, Gallina
Zhao, Jun
Hou, Teng
Comprehensive analysis of alternative polyadenylation regulators concerning CD276 and immune infiltration in bladder cancer
title Comprehensive analysis of alternative polyadenylation regulators concerning CD276 and immune infiltration in bladder cancer
title_full Comprehensive analysis of alternative polyadenylation regulators concerning CD276 and immune infiltration in bladder cancer
title_fullStr Comprehensive analysis of alternative polyadenylation regulators concerning CD276 and immune infiltration in bladder cancer
title_full_unstemmed Comprehensive analysis of alternative polyadenylation regulators concerning CD276 and immune infiltration in bladder cancer
title_short Comprehensive analysis of alternative polyadenylation regulators concerning CD276 and immune infiltration in bladder cancer
title_sort comprehensive analysis of alternative polyadenylation regulators concerning cd276 and immune infiltration in bladder cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9520876/
https://www.ncbi.nlm.nih.gov/pubmed/36175880
http://dx.doi.org/10.1186/s12885-022-10103-7
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