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Stepwise molecular mechanisms responsible for chemoresistance in bladder cancer cells

Chemotherapy resistance is an obstacle to cancer therapy and is considered a major cause of recurrence. Thus, understanding the mechanisms of chemoresistance is critical to improving the prognosis of patients. Here, we have established a stepwise gemcitabine-resistant T24 bladder cancer cell line to...

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Autores principales: Mun, Jeong-Yeon, Baek, Seung-Woo, Jeong, Mi-So, Jang, In-Hwan, Lee, Se-Ra, You, Jae-Young, Kim, Jeong-Ah, Yang, Gi-Eun, Choi, Yung-Hyun, Kim, Tae-Nam, Chu, In-Sun, Leem, Sun-Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640638/
https://www.ncbi.nlm.nih.gov/pubmed/36344487
http://dx.doi.org/10.1038/s41420-022-01242-8
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author Mun, Jeong-Yeon
Baek, Seung-Woo
Jeong, Mi-So
Jang, In-Hwan
Lee, Se-Ra
You, Jae-Young
Kim, Jeong-Ah
Yang, Gi-Eun
Choi, Yung-Hyun
Kim, Tae-Nam
Chu, In-Sun
Leem, Sun-Hee
author_facet Mun, Jeong-Yeon
Baek, Seung-Woo
Jeong, Mi-So
Jang, In-Hwan
Lee, Se-Ra
You, Jae-Young
Kim, Jeong-Ah
Yang, Gi-Eun
Choi, Yung-Hyun
Kim, Tae-Nam
Chu, In-Sun
Leem, Sun-Hee
author_sort Mun, Jeong-Yeon
collection PubMed
description Chemotherapy resistance is an obstacle to cancer therapy and is considered a major cause of recurrence. Thus, understanding the mechanisms of chemoresistance is critical to improving the prognosis of patients. Here, we have established a stepwise gemcitabine-resistant T24 bladder cancer cell line to understand the molecular mechanisms of chemoresistance within cancer cells. The characteristics of the stepwise chemoresistance cell line were divided into 4 phases (parental, early, intermediate, and late phases). These four phase cells showed increasingly aggressive phenotypes in vitro and in vivo experiments with increasing phases and revealed the molecular properties of the biological process from parent cells to phased gemcitabine-resistant cell line (GRC). Taken together, through the analysis of gene expression profile data, we have characterized gene set of each phase indicating the response to anticancer drug treatment. Specifically, we identified a multigene signature (23 genes including GATA3, APOBEC3G, NT5E, MYC, STC1, FOXD1, SMAD9) and developed a chemoresistance score consisting of that could predict eventual responsiveness to gemcitabine treatment. Our data will contribute to predicting chemoresistance and improving the prognosis of bladder cancer patients.
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spelling pubmed-96406382022-11-15 Stepwise molecular mechanisms responsible for chemoresistance in bladder cancer cells Mun, Jeong-Yeon Baek, Seung-Woo Jeong, Mi-So Jang, In-Hwan Lee, Se-Ra You, Jae-Young Kim, Jeong-Ah Yang, Gi-Eun Choi, Yung-Hyun Kim, Tae-Nam Chu, In-Sun Leem, Sun-Hee Cell Death Discov Article Chemotherapy resistance is an obstacle to cancer therapy and is considered a major cause of recurrence. Thus, understanding the mechanisms of chemoresistance is critical to improving the prognosis of patients. Here, we have established a stepwise gemcitabine-resistant T24 bladder cancer cell line to understand the molecular mechanisms of chemoresistance within cancer cells. The characteristics of the stepwise chemoresistance cell line were divided into 4 phases (parental, early, intermediate, and late phases). These four phase cells showed increasingly aggressive phenotypes in vitro and in vivo experiments with increasing phases and revealed the molecular properties of the biological process from parent cells to phased gemcitabine-resistant cell line (GRC). Taken together, through the analysis of gene expression profile data, we have characterized gene set of each phase indicating the response to anticancer drug treatment. Specifically, we identified a multigene signature (23 genes including GATA3, APOBEC3G, NT5E, MYC, STC1, FOXD1, SMAD9) and developed a chemoresistance score consisting of that could predict eventual responsiveness to gemcitabine treatment. Our data will contribute to predicting chemoresistance and improving the prognosis of bladder cancer patients. Nature Publishing Group UK 2022-11-07 /pmc/articles/PMC9640638/ /pubmed/36344487 http://dx.doi.org/10.1038/s41420-022-01242-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mun, Jeong-Yeon
Baek, Seung-Woo
Jeong, Mi-So
Jang, In-Hwan
Lee, Se-Ra
You, Jae-Young
Kim, Jeong-Ah
Yang, Gi-Eun
Choi, Yung-Hyun
Kim, Tae-Nam
Chu, In-Sun
Leem, Sun-Hee
Stepwise molecular mechanisms responsible for chemoresistance in bladder cancer cells
title Stepwise molecular mechanisms responsible for chemoresistance in bladder cancer cells
title_full Stepwise molecular mechanisms responsible for chemoresistance in bladder cancer cells
title_fullStr Stepwise molecular mechanisms responsible for chemoresistance in bladder cancer cells
title_full_unstemmed Stepwise molecular mechanisms responsible for chemoresistance in bladder cancer cells
title_short Stepwise molecular mechanisms responsible for chemoresistance in bladder cancer cells
title_sort stepwise molecular mechanisms responsible for chemoresistance in bladder cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640638/
https://www.ncbi.nlm.nih.gov/pubmed/36344487
http://dx.doi.org/10.1038/s41420-022-01242-8
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