硫氧还蛋白还原酶
金化合物
化学
硫氧还蛋白
程序性细胞死亡
作用机理
癌细胞
癌症
活性氧
药理学
酶
生物化学
组合化学
细胞凋亡
体外
生物
遗传学
作者
Yunlong Lu,Xiaoyan Ma,Xingyu Chang,Zhenlin Liang,Lin Lv,Min Shan,Qiuyue Lu,Zhenfan Wen,Ronald Gust,Wukun Liu
摘要
Metal complexes have demonstrated significant antitumor activities and platinum complexes are well established in the clinical application of cancer chemotherapy. However, the platinum-based treatment of different types of cancers is massively hampered by severe side effects and resistance development. Consequently, the development of novel metal-based drugs with different mechanism of action and pharmaceutical profile attracts modern medicinal chemists to design and synthesize novel metal-based agents. Among non-platinum anticancer drugs, gold complexes have gained considerable attention due to their significant antiproliferative potency and efficacy. In most situations, the gold complexes exhibit anticancer activities by targeting thioredoxin reductase (TrxR) or other thiol-rich proteins and enzymes and trigger cell death via reactive oxygen species (ROS). Interestingly, gold complexes were recently reported to elicit biochemical hallmarks of immunogenic cell death (ICD) as an ICD inducer. In this review, the recent progress of gold(I) and gold(III) complexes is comprehensively summarized, and their activities and mechanism of action are documented.
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