顺铂
膀胱癌
医学
癌症研究
抗性(生态学)
癌症
药理学
肿瘤科
内科学
化疗
生物
生态学
作者
Linjin Li,Chengpeng Li,Feilong Miao,Wu Chen,Xianghui Kong,R. Ye,Feng Wang
标识
DOI:10.2174/0118715206304668240729093158
摘要
BACKGROUND: Cisplatin is a key therapeutic agent for bladder cancer, yet the emergence of cisplatin resistance presents a significant clinical challenge. OBJECTIVE: This study aims to investigate the potential and mechanisms of cyclanoline (Cyc) in overcoming cisplatin resistance. METHODS: , subcutaneous tumor transplantation models in nude mice were established, assessing tumor volume and weight. Changes in bladder cancer tissues were observed through HE staining, and the p-STAT3 was assessed via WB and IHC. RESULTS: , tumor growth was significantly suppressed, with extensive tumor cell death. IHC and WB consistently showed a substantial downregulation of STAT3 phosphorylation. These changes were more pronounced when cisplatin and Cyc were administered in combination. CONCLUSION: JAK/STAT3 inhibition in bladder cancer, offering a potential clinical strategy to enhance cisplatin efficacy in treating bladder cancer.
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