Two novel silver(I) phenanthroline derivative complexes induce G2/M phase cycle arrest and apoptosis of MDA-MB-231 cancer cells by multiple mechanisms

被引:2
|
作者
Niu, Zong-ling [1 ]
Wu, Tian-Tian [1 ]
Wu, Yuan-yuan [1 ]
Zhou, Si-Han [1 ]
Li, Zhe [2 ,3 ]
Guo, Ji-Chao [1 ]
Zhou, Shu-Min [1 ]
Deng, Shi-Hui [1 ]
Xu, Jing-Yuan [2 ,3 ]
Xie, Ming-Jin [1 ]
机构
[1] Yunnan Univ, Sch Chem Sci & Technol, Kunming 650091, Yunnan, Peoples R China
[2] Tianjin Med Univ, Sch Pharm, Dept Chem Biol, Tianjin, Peoples R China
[3] Tianjin Med Univ, Sch Pharm, Tianjin Key Lab Technol Enabling Dev Clin Therapeu, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
anticancer; apoptosis; drugs; human breast cancer cells; silver complexes; CYTOTOXICITY;
D O I
10.1002/aoc.7123
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two novel silver(I) phenanthroline derivative complexes (P-235 and P-239) have been synthesized and characterized by IR, HPLC-MS, and (HNMR)-H-1. The cytotoxicity of two complexes exhibited significant cytotoxicity against human breast cancer (MDA-MB-231) cell line (IC50 = 0.48 +/- 0.01 and 0.12 +/- 0.01 mu M) and less toxicity than cisplatin by MTT assays. Furthermore, anticancer mechanistic studies showed that P-235 and P-239 induced G2/M phase cell cycle arrest to inhibit the growth of MDA-MB-231 cells. Flow cytometry analysis showed that MDA-MB-231 cells could be significantly induced to undergo apoptosis by P-235 and P-239. And P-235- and P-239-induced apoptosis was linked with reactive oxygen species (ROS) production. Further study revealed that P-235 and P-239 cause mitochondrial membrane potential depolarization and destroy mitochondrial membrane potential.
引用
收藏
页数:9
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