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Immune Profiling Reveals Molecular Classification and Characteristic in Urothelial Bladder Cancer

Urothelial bladder cancer (UBC) is the most common malignant tumor of the urinary system. Most patients do not benefit from treatment with immune checkpoint inhibitors, which are closely associated with immune profiling in the context of UBC. Therefore, we aimed to characterize the immune profile of...

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Autores principales: Yang, Li, Li, Aitian, Liu, Fengsen, Zhao, Qitai, Ji, Shaofei, Zhu, Wen, Yu, Weina, Zhang, Ru, Liu, Yaqing, Li, Wencai, Zhang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990773/
https://www.ncbi.nlm.nih.gov/pubmed/33777927
http://dx.doi.org/10.3389/fcell.2021.596484
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author Yang, Li
Li, Aitian
Liu, Fengsen
Zhao, Qitai
Ji, Shaofei
Zhu, Wen
Yu, Weina
Zhang, Ru
Liu, Yaqing
Li, Wencai
Zhang, Yi
author_facet Yang, Li
Li, Aitian
Liu, Fengsen
Zhao, Qitai
Ji, Shaofei
Zhu, Wen
Yu, Weina
Zhang, Ru
Liu, Yaqing
Li, Wencai
Zhang, Yi
author_sort Yang, Li
collection PubMed
description Urothelial bladder cancer (UBC) is the most common malignant tumor of the urinary system. Most patients do not benefit from treatment with immune checkpoint inhibitors, which are closely associated with immune profiling in the context of UBC. Therefore, we aimed to characterize the immune profile of UBC to identify different immune subtypes that may influence therapy choice. We identified four subtypes of UBC based on immune profiling including immune ignorant, cold tumor, immune inactive, and hot tumor. After excluding the cold tumor subtype because of its unique pathology distinct from the other types, a high correlation between patient survival and immune characteristics was observed. Most immune cell types had highly infiltrated the hot tumor subtype compared to other subtypes. Interestingly, although immune cells infiltrated the tumor microenvironment, they exhibited an exhaustion phenotype. CCL4 may be the key molecule functioning in immune cell infiltration in the hot tumor subtype. Moreover, neutrophils may function as an important suppressor in the tumor microenvironment of the immune ignorant and immune inactive subtypes. Furthermore, different tumor-intrinsic signaling pathways were involved in immune cell infiltration and exclusion in these four different subtypes. Immune profiling could serve as a prognostic biomarker for UBC, and has potential to guide treatment decisions in UBC. Targeting tumor-intrinsic signaling pathways may be a promising strategy to treat UBC.
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spelling pubmed-79907732021-03-26 Immune Profiling Reveals Molecular Classification and Characteristic in Urothelial Bladder Cancer Yang, Li Li, Aitian Liu, Fengsen Zhao, Qitai Ji, Shaofei Zhu, Wen Yu, Weina Zhang, Ru Liu, Yaqing Li, Wencai Zhang, Yi Front Cell Dev Biol Cell and Developmental Biology Urothelial bladder cancer (UBC) is the most common malignant tumor of the urinary system. Most patients do not benefit from treatment with immune checkpoint inhibitors, which are closely associated with immune profiling in the context of UBC. Therefore, we aimed to characterize the immune profile of UBC to identify different immune subtypes that may influence therapy choice. We identified four subtypes of UBC based on immune profiling including immune ignorant, cold tumor, immune inactive, and hot tumor. After excluding the cold tumor subtype because of its unique pathology distinct from the other types, a high correlation between patient survival and immune characteristics was observed. Most immune cell types had highly infiltrated the hot tumor subtype compared to other subtypes. Interestingly, although immune cells infiltrated the tumor microenvironment, they exhibited an exhaustion phenotype. CCL4 may be the key molecule functioning in immune cell infiltration in the hot tumor subtype. Moreover, neutrophils may function as an important suppressor in the tumor microenvironment of the immune ignorant and immune inactive subtypes. Furthermore, different tumor-intrinsic signaling pathways were involved in immune cell infiltration and exclusion in these four different subtypes. Immune profiling could serve as a prognostic biomarker for UBC, and has potential to guide treatment decisions in UBC. Targeting tumor-intrinsic signaling pathways may be a promising strategy to treat UBC. Frontiers Media S.A. 2021-03-11 /pmc/articles/PMC7990773/ /pubmed/33777927 http://dx.doi.org/10.3389/fcell.2021.596484 Text en Copyright © 2021 Yang, Li, Liu, Zhao, Ji, Zhu, Yu, Zhang, Liu, Li and Zhang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Yang, Li
Li, Aitian
Liu, Fengsen
Zhao, Qitai
Ji, Shaofei
Zhu, Wen
Yu, Weina
Zhang, Ru
Liu, Yaqing
Li, Wencai
Zhang, Yi
Immune Profiling Reveals Molecular Classification and Characteristic in Urothelial Bladder Cancer
title Immune Profiling Reveals Molecular Classification and Characteristic in Urothelial Bladder Cancer
title_full Immune Profiling Reveals Molecular Classification and Characteristic in Urothelial Bladder Cancer
title_fullStr Immune Profiling Reveals Molecular Classification and Characteristic in Urothelial Bladder Cancer
title_full_unstemmed Immune Profiling Reveals Molecular Classification and Characteristic in Urothelial Bladder Cancer
title_short Immune Profiling Reveals Molecular Classification and Characteristic in Urothelial Bladder Cancer
title_sort immune profiling reveals molecular classification and characteristic in urothelial bladder cancer
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990773/
https://www.ncbi.nlm.nih.gov/pubmed/33777927
http://dx.doi.org/10.3389/fcell.2021.596484
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