Mechanisms of cisplatin-induced ototoxicity and prevention

被引:417
|
作者
Rybak, Leonard P.
Whitworth, Craig A.
Mukherjea, Debashree
Rarakumar, Vickram
机构
[1] So Illinois Univ, Sch Med, Div Otolaryngol, Dept Surg, Springfield, IL 62794 USA
[2] So Illinois Univ, Dept Pharmacol, Carbondale, IL 62901 USA
关键词
cisplatin; reactive oxygen species; apoptosis; NADPH; oxidase;
D O I
10.1016/j.heares.2006.09.015
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
Cisplatin is a widely used chemotherapeutic agent to treat malignant disease. Unfortunately, ototoxicity occurs in a large percentage of patients treated with higher dose regimens. In animal studies and in human temporal bone investigations, several areas of the cochlea are damaged, including outer hair cells in the basal turn, spiral ganglion cells and the stria vascularis, resulting in hearing impairment. The mechanisms appear to involve the production of reactive oxygen species (ROS), which can trigger cell death. Approaches to chemoprevention include the administration of antioxidants to protect against ROS at an early stage in the ototoxic pathways and the application of agents that act further downstream in the cell death cascade to prevent apoptosis and hearing loss. This review summarizes recent data that shed new light on the mechanisms of cisplatin ototoxicity and its prevention. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:157 / 167
页数:11
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