Characterization and treatment of gemcitabine‐ and cisplatin‐resistant bladder cancer cells with a pan‐RAS inhibitor

Author:

Yoshino Hirofumi1ORCID,Yokoyama Seiya2,Tamai Motoki1,Okamura Shunsuke1,Iizasa Sayaka1,Sakaguchi Takashi1,Osako Yoichi1,Inoguchi Satoru1,Matsushita Ryosuke1,Yamada Yasutoshi1,Nakagawa Masayuki1,Tatarano Shuichi1,Tanimoto Akihide2,Enokida Hideki1ORCID

Affiliation:

1. Department of Urology, Graduate School of Medical and Dental Sciences Kagoshima University Japan

2. Department of Pathology, Graduate School of Medical and Dental Sciences Kagoshima University Japan

Abstract

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.

Funder

Japan Society for the Promotion of Science

Takeda Science Foundation

Publisher

Wiley

Subject

General Biochemistry, Genetics and Molecular Biology

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