Two novel chiral tetranucleate copper-based complexes: syntheses, crystal structures, inhibition of angiogenesis and the growth of human breast cancer in vitro and in vivo

被引:11
|
作者
Hou, Xiao-Xiao [1 ]
Ren, Ya-Ping [1 ]
Luo, Zhao-Hui [1 ]
Jiang, Bing-Li [1 ]
Lu, Tian-Tian [1 ]
Huang, Fu-Ping [2 ]
Qin, Xiu-Ying [1 ,2 ]
机构
[1] Guilin Med Univ, Coll Pharm, Dept Histol & Embryol, Guilin 541004, Guangxi, Peoples R China
[2] Guangxi Normal Univ, Sch Chem & Pharm, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Guangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
ANTICANCER ACTIVITY; TUMOR ANGIOGENESIS; DNA-BINDING; CYTOTOXICITY; CARBOPLATIN;
D O I
10.1039/d1dt02033a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The single crystals of two novel chiral tetranucleate copper(ii)-based complexes (TNCu-A and TNCu-B) containing l-methioninol-derived Schiff-bases were obtained. Their single structures were characterized by X-ray single crystal diffraction, infrared (IR) rays, elemental analysis, and liquid chromatography-mass spectrometry analysis. TNCu-A can effectively inhibit human umbilical vein endothelial cells (HUVECs) to form a tubular structure and it induces apoptosis of human triple-negative breast cancer MDA-MB-231 cells and HUVECs in vitro in a mitochondria dependent manner. Moreover, in vivo TNCu-A can remarkably inhibit the growth of triple-negative breast cancer from which MDA-MB-231 cells were xenografted into severely immunodeficient nude mice by inhibiting proliferation, inducing apoptosis of MDA-MB-231 cells by dramatically inhibiting the expression of the anti-apoptotic protein Bcl-2 and up-regulating the expressions of proapoptotic proteins caspase-9 and Bax, and simultaneously inhibiting tumor angiogenesis by decreasing the density of vascular endothelial cells and suppressing migration and even partially inducing apoptosis.
引用
收藏
页码:14684 / 14694
页数:11
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