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Characterization and treatment of gemcitabine‐ and cisplatin‐resistant bladder cancer cells with a pan‐RAS inhibitor
Combination chemotherapy with gemcitabine and cisplatin (GC) is recommended as the primary treatment for advanced bladder cancer (BC). However, the benefits of this approach are limited owing to the acquisition of drug resistance. Here, we found that gemcitabine‐resistant and cisplatin‐resistant BCs...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240337/ https://www.ncbi.nlm.nih.gov/pubmed/37079001 http://dx.doi.org/10.1002/2211-5463.13616 |
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author | Yoshino, Hirofumi Yokoyama, Seiya Tamai, Motoki Okamura, Shunsuke Iizasa, Sayaka Sakaguchi, Takashi Osako, Yoichi Inoguchi, Satoru Matsushita, Ryosuke Yamada, Yasutoshi Nakagawa, Masayuki Tatarano, Shuichi Tanimoto, Akihide Enokida, Hideki |
author_facet | Yoshino, Hirofumi Yokoyama, Seiya Tamai, Motoki Okamura, Shunsuke Iizasa, Sayaka Sakaguchi, Takashi Osako, Yoichi Inoguchi, Satoru Matsushita, Ryosuke Yamada, Yasutoshi Nakagawa, Masayuki Tatarano, Shuichi Tanimoto, Akihide Enokida, Hideki |
author_sort | Yoshino, Hirofumi |
collection | PubMed |
description | Combination chemotherapy with gemcitabine and cisplatin (GC) is recommended as the primary treatment for advanced bladder cancer (BC). However, the benefits of this approach are limited owing to the acquisition of drug resistance. Here, we found that gemcitabine‐resistant and cisplatin‐resistant BCs do not exhibit cross‐resistance, and that these BCs exhibit different mRNA patterns, as revealed using RNA sequence analysis. To overcome drug resistance, we used the newly developed pan‐RAS inhibitor Compound 3144. Compound 3144 inhibited cell viability through suppression of RAS‐dependent signaling in gemcitabine‐ and cisplatin‐resistant BCs. RNA sequencing revealed that several genes and pathways, particularly those related to the cell cycle, were significantly downregulated in Compound 3144‐treated BCs. These findings provide insights into potential therapeutic strategies for treating BC. |
format | Online Article Text |
id | pubmed-10240337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102403372023-06-06 Characterization and treatment of gemcitabine‐ and cisplatin‐resistant bladder cancer cells with a pan‐RAS inhibitor Yoshino, Hirofumi Yokoyama, Seiya Tamai, Motoki Okamura, Shunsuke Iizasa, Sayaka Sakaguchi, Takashi Osako, Yoichi Inoguchi, Satoru Matsushita, Ryosuke Yamada, Yasutoshi Nakagawa, Masayuki Tatarano, Shuichi Tanimoto, Akihide Enokida, Hideki FEBS Open Bio Research Articles Combination chemotherapy with gemcitabine and cisplatin (GC) is recommended as the primary treatment for advanced bladder cancer (BC). However, the benefits of this approach are limited owing to the acquisition of drug resistance. Here, we found that gemcitabine‐resistant and cisplatin‐resistant BCs do not exhibit cross‐resistance, and that these BCs exhibit different mRNA patterns, as revealed using RNA sequence analysis. To overcome drug resistance, we used the newly developed pan‐RAS inhibitor Compound 3144. Compound 3144 inhibited cell viability through suppression of RAS‐dependent signaling in gemcitabine‐ and cisplatin‐resistant BCs. RNA sequencing revealed that several genes and pathways, particularly those related to the cell cycle, were significantly downregulated in Compound 3144‐treated BCs. These findings provide insights into potential therapeutic strategies for treating BC. John Wiley and Sons Inc. 2023-04-29 /pmc/articles/PMC10240337/ /pubmed/37079001 http://dx.doi.org/10.1002/2211-5463.13616 Text en © 2023 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Yoshino, Hirofumi Yokoyama, Seiya Tamai, Motoki Okamura, Shunsuke Iizasa, Sayaka Sakaguchi, Takashi Osako, Yoichi Inoguchi, Satoru Matsushita, Ryosuke Yamada, Yasutoshi Nakagawa, Masayuki Tatarano, Shuichi Tanimoto, Akihide Enokida, Hideki Characterization and treatment of gemcitabine‐ and cisplatin‐resistant bladder cancer cells with a pan‐RAS inhibitor |
title | Characterization and treatment of gemcitabine‐ and cisplatin‐resistant bladder cancer cells with a pan‐RAS inhibitor |
title_full | Characterization and treatment of gemcitabine‐ and cisplatin‐resistant bladder cancer cells with a pan‐RAS inhibitor |
title_fullStr | Characterization and treatment of gemcitabine‐ and cisplatin‐resistant bladder cancer cells with a pan‐RAS inhibitor |
title_full_unstemmed | Characterization and treatment of gemcitabine‐ and cisplatin‐resistant bladder cancer cells with a pan‐RAS inhibitor |
title_short | Characterization and treatment of gemcitabine‐ and cisplatin‐resistant bladder cancer cells with a pan‐RAS inhibitor |
title_sort | characterization and treatment of gemcitabine‐ and cisplatin‐resistant bladder cancer cells with a pan‐ras inhibitor |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240337/ https://www.ncbi.nlm.nih.gov/pubmed/37079001 http://dx.doi.org/10.1002/2211-5463.13616 |
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