Suppr超能文献

紫杉醇诱导的不良反应:对多器官毒性及分子机制的见解

Paclitaxel-induced adverse effects: insights into multi-organ toxicities and molecular mechanisms.

作者信息

Naeem Antoinette G, Fawzi Sylvia F, Elmorsi Radwa M, George Mina Y

机构信息

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Ain Shams University, Cairo, 11566, Egypt.

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Badr University in Cairo (BUC), Cairo, Egypt.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2025 Aug 27. doi: 10.1007/s00210-025-04480-6.

Abstract

Paclitaxel (PTX), a member of the taxane family of anticancer drugs, is considered one of the most effective chemotherapeutic agents used worldwide. It is widely used in the treatment of solid tumors, including non-small-cell lung, colon, breast, ovarian, prostate, and bladder cancers. Its anticancer activity involves multiple mechanisms: mitotic arrest, mitochondrial damage, and apoptosis induction. Hence, being a non-targeted drug, PTX is associated with many types of toxicities, limiting its effectiveness and affecting the patient's quality of life. Unfortunately, this may result in treatment modifications or even discontinuation. The common clinical toxicities encountered with PTX include cognitive impairment, peripheral neuropathy, testicular toxicity, pulmonary toxicity, cardiotoxicity, hepatotoxicity, and nephrotoxicity. However, the underlying mechanisms of these toxicities remain elusive. This review article focuses on PTX-induced toxicities and the suggested detailed pathological mechanisms underlying each one.

摘要

紫杉醇(PTX)是紫杉烷类抗癌药物家族的一员,被认为是全球使用的最有效的化疗药物之一。它广泛用于治疗实体瘤,包括非小细胞肺癌、结肠癌、乳腺癌、卵巢癌、前列腺癌和膀胱癌。其抗癌活性涉及多种机制:有丝分裂停滞、线粒体损伤和凋亡诱导。因此,作为一种非靶向药物,PTX与多种毒性相关,限制了其有效性并影响患者的生活质量。不幸的是,这可能导致治疗调整甚至停药。PTX常见的临床毒性包括认知障碍、周围神经病变、睾丸毒性、肺毒性、心脏毒性、肝毒性和肾毒性。然而,这些毒性的潜在机制仍然难以捉摸。这篇综述文章聚焦于PTX诱导的毒性以及每种毒性背后建议的详细病理机制。

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