Apoptosis, autophagy, ferroptosis, and pyroptosis in cisplatin-induced ototoxicity and protective agents

Cisplatin is widely used to treat various solid tumors. However, its toxicity to normal tissues limits its clinical application, particularly due to its ototoxic effects, which can result in hearing loss in patients undergoing chemotherapy. While significant progress has been made in preclinical stu...

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Główni autorzy: Dingyuan Dai (Autor), Chao Chen (Autor), Chen Lu (Autor), Yu Guo (Autor), Qi Li (Autor), Chen Sun (Autor)
Format: Książka
Wydane: Frontiers Media S.A., 2024-09-01T00:00:00Z.
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100 1 0 |a Dingyuan Dai  |e author 
700 1 0 |a Dingyuan Dai  |e author 
700 1 0 |a Chao Chen  |e author 
700 1 0 |a Chao Chen  |e author 
700 1 0 |a Chen Lu  |e author 
700 1 0 |a Yu Guo  |e author 
700 1 0 |a Yu Guo  |e author 
700 1 0 |a Qi Li  |e author 
700 1 0 |a Qi Li  |e author 
700 1 0 |a Qi Li  |e author 
700 1 0 |a Chen Sun  |e author 
245 0 0 |a Apoptosis, autophagy, ferroptosis, and pyroptosis in cisplatin-induced ototoxicity and protective agents 
260 |b Frontiers Media S.A.,   |c 2024-09-01T00:00:00Z. 
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520 |a Cisplatin is widely used to treat various solid tumors. However, its toxicity to normal tissues limits its clinical application, particularly due to its ototoxic effects, which can result in hearing loss in patients undergoing chemotherapy. While significant progress has been made in preclinical studies to elucidate the cellular and molecular mechanisms underlying cisplatin-induced ototoxicity (CIO), the precise mechanisms remain unclear. Moreover, the optimal protective agent for preventing or mitigating cisplatin-induced ototoxicity has yet to be identified. This review summarizes the current understanding of the roles of apoptosis, autophagy, ferroptosis, pyroptosis, and protective agents in cisplatin-induced ototoxicity. A deeper understanding of these cell death mechanisms in the inner ear, along with the protective agents, could facilitate the translation of these agents into clinical therapeutics, help identify new therapeutic targets, and provide novel strategies for cisplatin-based cancer treatment. 
546 |a EN 
690 |a cisplatin 
690 |a ototoxicity 
690 |a apoptosis 
690 |a autophagy 
690 |a ferroptosis 
690 |a pyroptosis 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pharmacology, Vol 15 (2024) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fphar.2024.1430469/full 
787 0 |n https://doaj.org/toc/1663-9812 
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