Suppr超能文献

顺铂化疗与耳蜗损伤:多酚的耳保护和化疗增敏作用。

Cisplatin Chemotherapy and Cochlear Damage: Otoprotective and Chemosensitization Properties of Polyphenols.

机构信息

Department of Head and Neck Surgery, Università Cattolica Del Sacro Cuore, Rome, Italy.

Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

出版信息

Antioxid Redox Signal. 2022 Jun;36(16-18):1229-1245. doi: 10.1089/ars.2021.0183. Epub 2021 Dec 17.

Abstract

Cisplatin is an important component of treatment regimens for different cancers. Notwithstanding that therapeutic success often results from partial efficacy or stabilizing the disease, chemotherapy failure is driven by resistance to drug treatment and occurrence of side effects, such as progressive irreversible ototoxicity. Cisplatin's side effects, including ototoxicity, are often dose limiting. Cisplatin ototoxicity results from several mechanisms, including redox imbalance caused by reactive oxygen species production and lipid peroxidation, activation of inflammation, and p53 and its downstream pathways that culminate in apoptosis. Considerable efforts in research have targeted development of molecular interventions that can be concurrently administered with cisplatin or other chemotherapies to reduce side effect toxicities while preserving or enhancing the antineoplastic effects. Evidence from studies has indicated some polyphenols, such as curcumin, can help to regulate redox signaling and inflammatory effects. Furthermore, polyphenols can exert opposing effects in different types of tissues, that is, normal cells undergoing stressful conditions cancer cells. This review article summarizes evidence of curcumin antioxidant effect against cisplatin-induced ototoxicity that is converted to a pro-oxidant activity in cisplatin-treated cancer cells, thus providing an ideal chemosensitivity combined with otoprotection. Polyphenols can modulate the adaptive responses to stress in the cisplatin-exposed cochlea. These adaptive effects can result from the interaction/cross talk between the cell's defenses, inflammatory molecules, and the key signaling molecules of signal transducers and activators of transcription 3 (STAT-3), nuclear factor κ-B (NF-κB), p53, and nuclear factor erythroid 2-related factor 2 (Nrf-2). We provide molecular evidence for alternative strategies for chemotherapy with cisplatin addressing the otoprotection and chemosensitization properties of polyphenols. . 36, 1229-1245.

摘要

顺铂是多种癌症治疗方案的重要组成部分。尽管治疗的成功通常源于部分疗效或稳定疾病,但化疗失败是由于对药物治疗的耐药性和副作用的发生,如进行性不可逆的耳毒性。顺铂的副作用,包括耳毒性,通常是剂量限制的。顺铂耳毒性是由多种机制引起的,包括活性氧(ROS)产生和脂质过氧化引起的氧化还原失衡、炎症激活以及导致细胞凋亡的 p53 及其下游途径。研究人员进行了大量的努力,旨在开发分子干预措施,这些措施可以与顺铂或其他化疗药物同时使用,以减少副作用毒性,同时保留或增强抗肿瘤作用。研究证据表明,一些多酚类物质,如姜黄素,可以帮助调节氧化还原信号和炎症效应。此外,多酚类物质在不同类型的组织中可以发挥相反的作用,即在应激条件下正常细胞和癌细胞。 本文综述了姜黄素抗氧化作用对抗顺铂诱导耳毒性的证据,这种抗氧化作用在顺铂处理的癌细胞中转化为促氧化剂活性,从而提供了理想的化疗敏感性和耳保护作用。多酚类物质可以调节顺铂暴露耳蜗中的应激适应性反应。这些适应性效应可能是由于细胞防御、炎症分子以及信号转导和转录激活因子 3(STAT-3)、核因子 κ-B(NF-κB)、p53 和核因子红细胞 2 相关因子 2(Nrf-2)的关键信号分子之间的相互作用/交叉对话所致。 我们提供了分子证据,证明了用顺铂进行化疗的替代策略,解决了多酚类物质的耳保护和化疗增敏作用。. 36, 1229-1245.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验