Synthesis, DNA interaction and cytotoxicity studies of cis-{[1,2-bis(aminomethyl)cyclohexane]dihalo}platinum(II) complexes

被引:20
作者
de Mier-Vinue, Jordi [1 ,2 ]
Lorenzo, Julia [3 ]
Montana, Angel M. [1 ]
Moreno, Virtudes [2 ]
Aviles, Francesc X. [3 ]
机构
[1] Univ Barcelona, Dept Quim Organ, Unidad Quim Ind & Aplicada, Fac Quim, E-08028 Barcelona, Spain
[2] Univ Barcelona, Dept Quim Inorgan, Fac Quim, E-08028 Barcelona, Spain
[3] Univ Autonoma Barcelona, Inst Biotecnol & Biomed, E-08193 Barcelona, Spain
关键词
platinum(II) complexes; circular dichroism; electrophoresis; atomic force microscopy; HL-60 cell line;
D O I
10.1016/j.jinorgbio.2007.12.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of platinum compounds with an analogue structure to cisplatin have been synthesized and their biological activity against HL-60 cancer cell line has been studied. The interaction with DNA was evaluated by circular dichroism (CD), electrophoresis and atomic force microscopy (AFM) techniques showing slight but significant structure-dependent differences among the evaluated complexes. The cytotoxicity assays afforded interesting relationships between the structure and the biological activity, thus, a better antiproliferative activity was observed for the complexes with higher hydrophobicity: the methoxylated complexes showed better activity than the hydroxylated ones (17 versus 20 and 19 versus 21). Especially compound 22 having a fatty acid subunit presented a promising cytotoxic activity. On the other hand, dichloro complexes 12 and 13 had better activities than the diiodo complexes, probably due to their better metabolic stability. Between both dichloro complexes the aromatic one showed much higher activity, which could be rationalized on the basis of the intercalating ability of the benzene ring. The flow cytometry assays indicated that most of the complexes induced the cell death by apoptosis except for aromatic compound 12 and the lipophilic compound 22 that induced preferably a mechanism of necrosis. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:973 / 987
页数:15
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