Elafibranor 成为治疗非肌层浸润性膀胱癌的潜在化疗药物

Wang Wang , Danni Shan , Guanyi Wang , Xiongmin Mao , Wenjie You , Xiaolong Wang , Zijian Wang
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引用次数: 0

摘要

在治疗非肌层浸润性膀胱癌(NMIBC)时,一些临床指南强烈推荐进行膀胱内灌注化疗。然而,细胞毒性化疗药物会产生一系列副作用,极大地限制了其应用范围。在此,研究人员提出了一种饥饿疗法策略,并验证了依拉非尼(ELA)是一种治疗非肌层浸润性膀胱癌的安全化疗药物。结果表明,20 μM ELA足以抑制膀胱癌细胞的增殖和迁移,并增加细胞内活性氧(ROS)的水平。此外,2 毫克/千克 ELA 治疗通过抑制增殖和诱导凋亡阻断了免疫缺陷模型中原发性肿瘤的生长,并改善了免疫功能正常模型小鼠的存活时间。ELA 10 mg/kg 以下的治疗符合一般安全性要求。我们还建立了一个源自患者的条件重编程细胞(CRC)模型,以评估ELA的临床转化潜力。ELA的抗肿瘤效果和抗肿瘤特异性得到了证实。这项工作不仅为 NMIBC 找到了一种有前景的化疗药物,还为药物发现提供了一个潜在的方法体系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Elafibranor emerged as a potential chemotherapeutic drug for non-muscle invasive bladder cancer

Intravesical infusion of chemotherapeutics is highly recommended by several clinical guidelines for treating nonmuscle invasive bladder cancer (NMIBC). However, cytotoxic chemotherapeutics can cause a series of side effects, which greatly limits their application. Herein, a starvation therapy strategy was proposed, and elafibranor (ELA) was validated as a safe chemotherapeutic for NMIBC. The results showed that 20 μM ELA was sufficient to inhibit the proliferation and migration of bladder cancer cells and increase the level of intracellular reactive oxygen species (ROS). Furthermore, 2 mg/kg ELA treatment blocked the growth of primary tumors in an immunodeficient model by inhibiting proliferation and inducing apoptosis and improved the survival time of immunocompetent model mice. ELA treatment up to 10 mg/kg met the general safety requirements. We also established a patient-derived conditional reprogramming cell (CRC) model to assess the clinical translational potential of ELA. The antitumor effect and antitumor specificity of ELA treatment were confirmed. This work not only identified a promising chemotherapeutic for NMIBC but also provided a potential methodological system for drug discovery.

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来源期刊
Cell insight
Cell insight Neuroscience (General), Biochemistry, Genetics and Molecular Biology (General), Cancer Research, Cell Biology
CiteScore
2.70
自引率
0.00%
发文量
0
审稿时长
35 days
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