MOE Key Laboratory of Laser Life Science & Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China; Guangdong Provincial Key Laboratory of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China.
Department of Otorhinolaryngology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
Eur J Pharm Biopharm. 2021 Jun;163:60-71. doi: 10.1016/j.ejpb.2021.03.008. Epub 2021 Mar 26.
Cisplatin is a highly effective antitumor drug generally used in the treatment of solid malignant tumors. However, cisplatin causes severe side effects such as bone marrow depression, nephrotoxicity, and ototoxicity, thus limiting its clinical application. The incidence of ototoxicity induced by cisplatin ranges from 20% to 70%, and it usually manifests as a progressive, bilateral and irreversible hearing loss. Although the etiology of cisplatin-induced ototoxicity remains unclear, an increasing body of evidence suggests that the ototoxicity of cisplatin is mainly related to the production of reactive oxygen species and activation of apoptotic pathway in cochlear tissues. Many drugs have been well proved to protect cisplatin-induced hearing loss in vitro and in vivo. However, the anti-tumor effect of cisplatin is also weakened by systemic administration of those drugs for hearing protection, especially antioxidants. Therefore, establishing a local administration strategy contributes to the otoprotection without affecting the effect of cisplatin. This review introduces the pathology of ototoxicity caused by cisplatin, and focuses on recent developments in the mechanisms and protective strategies of cisplatin-induced ototoxicity.
顺铂是一种高效的抗肿瘤药物,通常用于治疗实体恶性肿瘤。然而,顺铂会引起严重的副作用,如骨髓抑制、肾毒性和耳毒性,从而限制了其临床应用。顺铂引起的耳毒性的发生率为 20%至 70%,通常表现为进行性、双侧和不可逆的听力损失。尽管顺铂诱导的耳毒性的病因尚不清楚,但越来越多的证据表明,顺铂的耳毒性主要与耳蜗组织中活性氧的产生和凋亡途径的激活有关。许多药物已被证明可在体外和体内保护顺铂诱导的听力损失。然而,这些用于听力保护的药物的全身给药也会减弱顺铂的抗肿瘤作用,尤其是抗氧化剂。因此,建立局部给药策略有助于在不影响顺铂疗效的情况下进行耳保护。本文介绍了顺铂引起的耳毒性的病理学,并重点介绍了顺铂诱导的耳毒性的机制和保护策略的最新进展。