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YAP1 activation is associated with the progression and response to immunotherapy of non-muscle invasive bladder cancer

BACKGROUND: Despite the availability of several treatments for non-muscle-invasive bladder cancer (NMIBC), many patients are still not responsive to treatments, and the disease progresses. A new prognostic classifier can differentiate between treatment response and progression, and it could be used...

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Autores principales: Baek, Seung-Woo, Mun, Jeong-Yeon, Jang, In-Hwan, Yang, Gi-Eun, Jeong, Mi-So, Kim, Seon-Kyu, Nam, Jong-Kil, Chu, In-Sun, Leem, Sun-Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166372/
https://www.ncbi.nlm.nih.gov/pubmed/35665684
http://dx.doi.org/10.1016/j.ebiom.2022.104092
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author Baek, Seung-Woo
Mun, Jeong-Yeon
Jang, In-Hwan
Yang, Gi-Eun
Jeong, Mi-So
Kim, Seon-Kyu
Nam, Jong-Kil
Chu, In-Sun
Leem, Sun-Hee
author_facet Baek, Seung-Woo
Mun, Jeong-Yeon
Jang, In-Hwan
Yang, Gi-Eun
Jeong, Mi-So
Kim, Seon-Kyu
Nam, Jong-Kil
Chu, In-Sun
Leem, Sun-Hee
author_sort Baek, Seung-Woo
collection PubMed
description BACKGROUND: Despite the availability of several treatments for non-muscle-invasive bladder cancer (NMIBC), many patients are still not responsive to treatments, and the disease progresses. A new prognostic classifier can differentiate between treatment response and progression, and it could be used as a very important tool in patient decision-making regarding treatment options. In this study, we focused on the activation of Yes-associated protein 1 (YAP1), which is known to play a pivotal role in tumour progression and serves as a factor contributing to the mechanism of resistance to various relevant therapeutic agents. We further evaluated its potential as a novel prognostic agent. METHODS: We identified YAP1-associated gene signatures based on UC3-siYAP1 cells (n=8) and NMIBC cohort (n=460). Cross-validation was performed using 5 independent bladder cancer patient cohorts (n=1006). We also experimentally validated the changes of gene expression levels representing each subgroup. FINDINGS: The 976-gene signature based on YAP1-activation redefined three subgroups and had the benefits of Bacillus Calmette-Guérin (BCG) treatment in patients with NMIBC (hazard ratio 3.32, 95% CI 1.29-8.56, p = 0.01). The integrated analysis revealed that YAP1 activation was associated with the characterization of patients with high-risk NMIBC and the response to immunotherapy. INTERPRETATION: This study suggests that YAP1 activation has an important prognostic effect on bladder cancer progression and might be useful in the selection of immunotherapy. FUNDING: A funding list that contributed to this research can be found in the Acknowledgements section.
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spelling pubmed-91663722022-06-22 YAP1 activation is associated with the progression and response to immunotherapy of non-muscle invasive bladder cancer Baek, Seung-Woo Mun, Jeong-Yeon Jang, In-Hwan Yang, Gi-Eun Jeong, Mi-So Kim, Seon-Kyu Nam, Jong-Kil Chu, In-Sun Leem, Sun-Hee eBioMedicine Articles BACKGROUND: Despite the availability of several treatments for non-muscle-invasive bladder cancer (NMIBC), many patients are still not responsive to treatments, and the disease progresses. A new prognostic classifier can differentiate between treatment response and progression, and it could be used as a very important tool in patient decision-making regarding treatment options. In this study, we focused on the activation of Yes-associated protein 1 (YAP1), which is known to play a pivotal role in tumour progression and serves as a factor contributing to the mechanism of resistance to various relevant therapeutic agents. We further evaluated its potential as a novel prognostic agent. METHODS: We identified YAP1-associated gene signatures based on UC3-siYAP1 cells (n=8) and NMIBC cohort (n=460). Cross-validation was performed using 5 independent bladder cancer patient cohorts (n=1006). We also experimentally validated the changes of gene expression levels representing each subgroup. FINDINGS: The 976-gene signature based on YAP1-activation redefined three subgroups and had the benefits of Bacillus Calmette-Guérin (BCG) treatment in patients with NMIBC (hazard ratio 3.32, 95% CI 1.29-8.56, p = 0.01). The integrated analysis revealed that YAP1 activation was associated with the characterization of patients with high-risk NMIBC and the response to immunotherapy. INTERPRETATION: This study suggests that YAP1 activation has an important prognostic effect on bladder cancer progression and might be useful in the selection of immunotherapy. FUNDING: A funding list that contributed to this research can be found in the Acknowledgements section. Elsevier 2022-06-02 /pmc/articles/PMC9166372/ /pubmed/35665684 http://dx.doi.org/10.1016/j.ebiom.2022.104092 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Baek, Seung-Woo
Mun, Jeong-Yeon
Jang, In-Hwan
Yang, Gi-Eun
Jeong, Mi-So
Kim, Seon-Kyu
Nam, Jong-Kil
Chu, In-Sun
Leem, Sun-Hee
YAP1 activation is associated with the progression and response to immunotherapy of non-muscle invasive bladder cancer
title YAP1 activation is associated with the progression and response to immunotherapy of non-muscle invasive bladder cancer
title_full YAP1 activation is associated with the progression and response to immunotherapy of non-muscle invasive bladder cancer
title_fullStr YAP1 activation is associated with the progression and response to immunotherapy of non-muscle invasive bladder cancer
title_full_unstemmed YAP1 activation is associated with the progression and response to immunotherapy of non-muscle invasive bladder cancer
title_short YAP1 activation is associated with the progression and response to immunotherapy of non-muscle invasive bladder cancer
title_sort yap1 activation is associated with the progression and response to immunotherapy of non-muscle invasive bladder cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9166372/
https://www.ncbi.nlm.nih.gov/pubmed/35665684
http://dx.doi.org/10.1016/j.ebiom.2022.104092
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