Li Fei, Zheng Zaosong, Chen Wei, Li Dongqing, Zhang Henghui, Zhu Yuanchao, Mo Qixin, Zhao Xinlei, Fan Qin, Deng Fan, Han Conghui, Tan Wanlong
Department of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Department of Urology, Institute of Precision Medicine, Zigong Forth People's Hospital, Zigong, Sichuan, China.
Drug Resist Updat. 2023 May;68:100938. doi: 10.1016/j.drup.2023.100938. Epub 2023 Feb 9.
Bladder cancer is one of the most common malignancies in the world. Cisplatin is one of the most potent and widely used anticancer drugs and has been employed in several malignancies. Cisplatin-based combination chemotherapies have become important adjuvant therapies for bladder cancer patients. Cisplatin-based treatment often results in the development of chemoresistance, leading to therapeutic failure and limiting its application and effectiveness in bladder cancer. To develop improved and more effective cancer therapy, research has been conducted to elucidate the underlying mechanism of cisplatin resistance. Epigenetic modifications have been demonstrated involved in drug resistance to chemotherapy, and epigenetic biomarkers, such as urine tumor DNA methylation assay, have been applied in patients screening or monitoring. Here, we provide a systematic description of epigenetic mechanisms, including DNA methylation, noncoding RNA regulation, m6A modification and posttranslational modifications, related to cisplatin resistance in bladder cancer.
膀胱癌是世界上最常见的恶性肿瘤之一。顺铂是最有效的且广泛使用的抗癌药物之一,已被用于多种恶性肿瘤的治疗。基于顺铂的联合化疗已成为膀胱癌患者重要的辅助治疗方法。基于顺铂的治疗常常导致化疗耐药的发生,从而导致治疗失败,并限制了其在膀胱癌治疗中的应用和疗效。为了开发改进的、更有效的癌症治疗方法,人们开展了相关研究以阐明顺铂耐药的潜在机制。表观遗传修饰已被证明与化疗耐药有关,并且表观遗传生物标志物,如尿液肿瘤DNA甲基化检测,已被应用于患者筛查或监测。在此,我们系统地描述了与膀胱癌顺铂耐药相关的表观遗传机制,包括DNA甲基化、非编码RNA调控、m6A修饰和翻译后修饰。