Zinc-binding compounds induce cancer cell death via distinct modes of action

被引:60
作者
Ding, Wei-Qun [1 ]
Yu, Hai-Jun [3 ]
Lind, Stuart E. [2 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Pathol, Oklahoma City, OK 73104 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Med, Aurora, CO 80045 USA
[3] Wuhan Univ, Zhongnan Hosp, Dept Radiochemotherapy, Wuhan, Peoples R China
关键词
Clioquinol; PDTC; TPEN; Chemotherapeutic; A2780;
D O I
10.1016/j.canlet.2008.06.011
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Metal-binding compounds have been shown to have anticancer activity and are being evaluated clinically as anticancer agents. We have recently found that a zinc-binding compound, 5-chloro-7-iodo-8-hydroxyquinoline (clioquinol), kills cancer cells by transporting zinc into the cells. We therefore compared the action of clioquinol with two other cytotoxic zinc-binding compounds, N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) and pyrrolidine dithiocarbamate (PDTC). We demonstrate that metal-binding compounds can be subclassified based upon the reversibility of their cytotoxicity by metal supplementation and their modes of action. Understanding the mechanisms whereby metal-binding compounds affect cell behavior may aid in their optimization for clinical use. (c) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:251 / 259
页数:9
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