Suppr超能文献

靶向铁死亡的具有抗癌作用的中药研究进展综述

A review on the research progress of traditional Chinese medicine with anti-cancer effect targeting ferroptosis.

作者信息

Wang Longyan, Huang Huiming, Li Xingxing, Ouyang Lishan, Wei Xuejiao, Xie Jinxin, Liu Dongxiao, Tan Peng, Hu Zhongdong

机构信息

Modern Research Center for Traditional Chinese Medicine, Beijing Research Institute of Chinese Medicine, Beijing University of Chinese Medicine, No. 11 North 3Rd Ring East Road, Chaoyang District, Beijing, 100029, People's Republic of China.

Dongfang Hospital, Beijing University of Chinese Medicine, Beijing, 100078, China.

出版信息

Chin Med. 2023 Oct 13;18(1):132. doi: 10.1186/s13020-023-00838-1.

Abstract

Ferroptosis is a non-apoptotic form of regulated cell death characterized by iron-dependent lipid peroxidation. It can be triggered by various mechanisms, including the glutathione peroxidase 4 (GPX4)-glutathione (GSH) axis, iron metabolism, lipid metabolism, the GTP cyclohydrolase 1 (GCH1)-tetrahydrobiopterin (BH4) pathway, and the ferroptosis suppressor protein 1 (FSP1)-coenzyme Q10 axis. The redox balance is disrupted when ferroptosis occurs in cells, which is fatal to cancer cells. Additionally, some tumor-associated genes are involved in ferroptosis. Hence, targeting ferroptosis might be an effective strategy for treating cancer. Several small-molecule compounds exhibit anti-tumor effects through ferroptosis, including sorafenib and altretamine, which induce ferroptosis by inhibiting System-Xc and GPX4 respectively, but many problems, such as poor druggability, still exist. Some studies have shown that many traditional Chinese medicine (TCM) induce ferroptosis by inhibiting GPX4, solute carrier family 7 member 11 (SLC7A11), and nuclear factor (erythroid-derived 2)-like 2 (Nrf2), or by increasing the expression of Acyl-CoA synthetase long-chain family member 4 (ACSL4), transferrin (TF), and transferrin receptor 1 (TFR1). These changes can lead to the lysosomal degradation of ferritin, accumulation of iron, lipid peroxidation and the production of reactive oxygen species (ROS), which in turn can promote anti-tumor activities or synergistic effects with chemotherapeutic drugs. In this study, we elucidated the underlying mechanisms of ferroptosis, and the anti-tumor pharmacology of TCM targeting ferroptosis including prescriptions, Chinese herbs, extracts, and natural compounds. Our findings might act as valuable reference for research on anti-tumor drugs targeting ferroptosis, especially those drugs developed from TCM.

摘要

铁死亡是一种非凋亡形式的程序性细胞死亡,其特征是铁依赖性脂质过氧化。它可由多种机制触发,包括谷胱甘肽过氧化物酶4(GPX4)-谷胱甘肽(GSH)轴、铁代谢、脂质代谢、GTP环水解酶1(GCH1)-四氢生物蝶呤(BH4)途径以及铁死亡抑制蛋白1(FSP1)-辅酶Q10轴。当细胞发生铁死亡时,氧化还原平衡被破坏,这对癌细胞是致命的。此外,一些肿瘤相关基因也参与铁死亡。因此,靶向铁死亡可能是治疗癌症的有效策略。几种小分子化合物通过铁死亡发挥抗肿瘤作用,包括索拉非尼和六甲蜜胺,它们分别通过抑制Xc系统和GPX4诱导铁死亡,但仍存在许多问题,如成药性能差。一些研究表明,许多中药通过抑制GPX4、溶质载体家族7成员11(SLC7A11)和核因子(红系衍生2)样2(Nrf2),或通过增加酰基辅酶A合成酶长链家族成员4(ACSL4)、转铁蛋白(TF)和转铁蛋白受体1(TFR1)的表达来诱导铁死亡。这些变化可导致铁蛋白的溶酶体降解、铁的积累、脂质过氧化和活性氧(ROS)的产生,进而促进抗肿瘤活性或与化疗药物产生协同作用。在本研究中,我们阐明了铁死亡的潜在机制,以及靶向铁死亡的中药的抗肿瘤药理学,包括方剂、中药材、提取物和天然化合物。我们的发现可能为靶向铁死亡的抗肿瘤药物研究,尤其是从中药开发的药物研究提供有价值的参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e83d/10571466/e5e18ebd6f2f/13020_2023_838_Fig1_HTML.jpg

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