钌
细胞凋亡
钌红
诱导剂
内质网
化学
细胞生物学
合理设计
DNA损伤
体外
体内
线粒体
DNA
信号转导
生物化学
生物
钙
基因
催化作用
遗传学
有机化学
作者
Kangdi Zheng,Qiong Wu,Chengxi Wang,Tan Wei-jun,Wenjie Mei
出处
期刊:Anti-cancer Agents in Medicinal Chemistry
[Bentham Science]
日期:2017-01-01
卷期号:17 (1): 29-39
被引量:20
标识
DOI:10.2174/1871520616666160622085441
摘要
Herein, the development of ruthenium complexes as potential apoptosis inducers, as well as their underlying mechanism has been reviewed. In recent years, various ruthenium complexes have been designed and their in vitro and in vivo inhibitory activities against various types of tumor cells have been evaluated extensively. It’s demonstrated that ruthenium complexes can induce apoptosis of tumor cells through the signal pathway of mitochondria-mediated, death receptor-mediated, and/or endoplasmic reticulum (ER) stress pathways. Alternately, the binding behavior of these ruthenium(II) complexes with DNA, especially with Gquadruplex DNA may play a key role in the DNA damage of tumor cells, and thus provides a versatile tool to rational design novel ruthenium complexes with high activity and selectivity.
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