A mixed-ligand copper(II) complex that inhibits growth and induces apoptosis by DNA targeting in human epithelial cervical cancer cells

被引:4
|
作者
Ma, Zhong-Ying [1 ]
Qiao, Zheng [1 ]
Wang, Dong-Bo [1 ]
Hou, Xuan [1 ]
Qiao, Xin [1 ]
Xie, Cheng-Zhi [1 ]
Qiang, Zhao-Yan [2 ]
Xu, Jing-Yuan [1 ]
机构
[1] Tianjin Med Univ, Sch Pharm, Tianjin Key Lab Technol Enabling Dev Clin Therape, Tianjin 300070, Peoples R China
[2] Tianjin Med Univ, Sch Basic Med, Tianjin 300070, Peoples R China
基金
中国国家自然科学基金;
关键词
anticancer; copper(II) complex; crystal structure; mixed ligand; SCHIFF-BASE COMPLEXES; BOVINE SERUM-ALBUMIN; NUCLEASE ACTIVITY; CLEAVAGE ACTIVITY; DNA/BSA BINDING; METAL-COMPLEXES; CYTOTOXICITY; 1,10-PHENANTHROLINE; DAMAGE; THERAPEUTICS;
D O I
10.1002/aoc.3651
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A new mixed-ligand copper(II) complex, [Cu(L)(phen)]center dot MeOH (L = 4-chloro-2[(2-hydroxyphenyl)iminomethyl]phenol), was synthesized. It belongs to the orthorhombic crystal system and Cu(II) is five-coordinated in a seriously distorted square pyramidal geometry. DNA binding experiments confirmed an intercalative mode of interaction of the complex with calf thymus DNA. In a DNA cleavage experiment with the complex, as hydrogen peroxide was involved, oxidative DNA cleavage occurred and double-stranded breaks even appeared at certain concentration. The strong interaction with bovine serum albumin suggested that the complex might be transported by protein. The complex exhibited more significant cytotoxicity in HeLa cells (IC50 = 0.46 +/- 0.01 mu M) for 48 h, compared with cisplatin (10.61 +/- 0.86 mu M). This work indicated that the complex could induce apoptosis in a dose-dependent manner and was associated with cell cycle arrest to some extent. Being consistent with the results of DNA cleavage experiment, comet assay indicated that the complex induced severe DNA fragmentation. The results showed the production of reactive oxygen species increased with increasing concentration of the complex. The complex was suggested to be capable of promoting HeLa cell apoptosis through an oxidative DNA damage pathway.
引用
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页数:11
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