半胱天冬酶抑制剂而非c-Jun氨基末端激酶抑制剂疗法可预防顺铂诱导的听力损失。
Caspase inhibitors, but not c-Jun NH2-terminal kinase inhibitor treatment, prevent cisplatin-induced hearing loss.
作者信息
Wang Jing, Ladrech Sabine, Pujol Remy, Brabet Philippe, Van De Water Thomas R, Puel Jean-Luc
机构信息
Institut National de la Santé et de la Recherche Medicale-UMR 583 and Université de Montpellier 1, Physiopathologie et thérapie des déficits sensoriels et moteurs, Montpellier, France.
出版信息
Cancer Res. 2004 Dec 15;64(24):9217-24. doi: 10.1158/0008-5472.CAN-04-1581.
Cisplatin (CDDP) is a highly effective chemotherapeutic agent but with significant ototoxic side effects. Apoptosis is an important mechanism of cochlear hair cell loss following exposure to an ototoxic level of CDDP. This study examines intracellular pathways involved in hair cell death induced by CDDP exposure in vivo to develop effective therapeutic strategies to protect the auditory receptor from CDDP-initiated hearing loss. Guinea pigs were treated with systemic administration of CDDP. Cochlear hair cells from CDDP-treated animals exhibited classic apoptotic alterations in their morphology. Several important signaling events that regulate the death of CDDP-injured cochlear hair cells were identified. CDDP treatment induced the activation and redistribution of cytosolic Bax and the release of cytochrome c from injured mitochondria. Activation of caspase-9 and caspase-3, but not caspase-8, was detected after treatment with CDDP, and the cleavage of fodrin by activated caspase-3 was observed within damaged hair cells. Intracochlear perfusions with caspase-3 inhibitor (z-DEVD-fmk) and caspase-9 inhibitor (z-LEHD-fmk) prevent hearing loss and loss of sensory cells, but caspase-8 inhibitor (z-IETD-fmk) and cathepsin B inhibitor (z-FA-fmk) do not. Although the stress-activated protein kinase/c-Jun NH(2)-terminal kinase (JNK) signaling pathway is activated in response to CDDP toxicity, intracochlear perfusion of d-JNKI-1, a JNK inhibitor, did not protect against CDDP ototoxicity but instead potentiated the ototoxic effects of CDDP. The results of the present study show that blocking a critical step in apoptosis may be a useful strategy to prevent harmful side effects of CDDP ototoxicity in patients having to undergo chemotherapy.
顺铂(CDDP)是一种高效的化疗药物,但具有显著的耳毒性副作用。细胞凋亡是暴露于耳毒性水平的顺铂后耳蜗毛细胞损失的重要机制。本研究考察体内顺铂暴露诱导毛细胞死亡所涉及的细胞内信号通路,以制定有效的治疗策略来保护听觉感受器免受顺铂引发的听力损失。豚鼠接受全身顺铂给药治疗。来自顺铂处理动物的耳蜗毛细胞在形态上表现出典型的凋亡改变。确定了几个调节顺铂损伤的耳蜗毛细胞死亡的重要信号事件。顺铂处理诱导胞质Bax的激活和重新分布以及细胞色素c从受损线粒体的释放。顺铂处理后检测到caspase-9和caspase-3的激活,但未检测到caspase-8的激活,并且在受损毛细胞内观察到活化的caspase-3对血影蛋白的切割。耳蜗内灌注caspase-3抑制剂(z-DEVD-fmk)和caspase-9抑制剂(z-LEHD-fmk)可预防听力损失和感觉细胞损失,但caspase-8抑制剂(z-IETD-fmk)和组织蛋白酶B抑制剂(z-FA-fmk)则不能。尽管应激激活蛋白激酶/c-Jun氨基末端激酶(JNK)信号通路在响应顺铂毒性时被激活,但耳蜗内灌注JNK抑制剂d-JNKI-1并不能预防顺铂耳毒性,反而增强了顺铂的耳毒性作用。本研究结果表明,阻断凋亡中的关键步骤可能是预防必须接受化疗的患者顺铂耳毒性有害副作用的有用策略。