Structure and biological properties of mixed-ligand Cu(II) Schiff base complexes as potential anticancer agents

被引:104
作者
Gou, Yi [1 ]
Li, Jinlong [1 ]
Fan, Boyi [1 ]
Xu, Bohui [1 ]
Zhou, Min [1 ]
Yang, Feng [1 ,2 ]
机构
[1] Nantong Univ, Sch Pharm, Nantong, Jiangsu, Peoples R China
[2] Guangxi Normal Univ, State Key Lab Chem & Mol Engn Med Resources, Minist Sci & Technol China, Guilin, Guangxi, Peoples R China
关键词
Aroylhydrazone Cu(II) complexes; Anti-metastatic activity; Anticancer activity; Anticancer mechanism; COPPER(II) COMPLEXES; ANTITUMOR-ACTIVITY; DNA-BINDING; POLYPYRIDYL COMPLEXES; CRYSTAL-STRUCTURES; CANCER-CELLS; CLEAVAGE; CYTOTOXICITY; IDENTIFICATION; MECHANISMS;
D O I
10.1016/j.ejmech.2017.04.026
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We synthesized two mixed-ligand Cu(II) complexes containing different aroylhydrazone ligands and a pyridine co-ligand, namely, [Cu(L1)(Py)] (Cl) and [Cu(L2)(Py)(Br)] (C2) (L1 = (E)-2-hydroxy-W-((2-hydroxynaphthalen-1-yl)methylene)benzohydrazide, Py = pyridine, L2 = (E)-2-hydroxy-W-(phenyl(pyridin-2-yl)methylene)benzohydrazide), and assessed their chemical and biological properties to understand their marked activity. C2 showed better anticancer activity than Cl in various human cancer cell lines, including the cisplatin-resistant lung cancer cell line A549cisR. Both Cu(II) complexes, especially C2, displayed promising anti-metastatic activity against HepG2 cells. Spectroscopic titration and agarose gel electrophoresis experiments indicated that C2 exhibited binding affinity toward calf-thymus DNA and efficient pBR322 DNA-cleaving ability. Further mechanistic studies showed that C2 effectively induced DNA damage and thus led to cell cycle arrest at the G2/M phase, and also stimulated mitochondrial dysfunction mediated by reactive oxygen species and caspase-dependent apoptosis. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:207 / 217
页数:11
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