Overcoming cisplatin resistance using gold(III) mimics: Anticancer activity of novel gold(III) polypyridyl complexes

被引:32
|
作者
Palanichamy, Kamalakannan [2 ]
Sreejayan, Nair [3 ,4 ]
Ontko, Allyn C. [1 ]
机构
[1] Arkansas State Univ, Dept Chem & Phys, State Univ, AR 72467 USA
[2] Ohio State Univ, Med Ctr, Dept Radiat Oncol, Columbus, OH 43210 USA
[3] Univ Wyoming, Sch Pharm, Div Pharmaceut Sci, Laramie, WY 82071 USA
[4] Univ Wyoming, Ctr Cardiovasc Res & Alternat Med, Laramie, WY 82071 USA
关键词
Gold(III); Au(III); Polypyridyl; Cellular uptake; DNA binding affinity; Anticancer; HUMAN OVARIAN-CANCER; DNA-BINDING PROPERTIES; SOLUTION CHEMISTRY; P53-DEPENDENT APOPTOSIS; BASE MISMATCHES; CARCINOMA CELLS; CYTOTOXICITY; P53; AGENTS; DEATH;
D O I
10.1016/j.jinorgbio.2011.08.013
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
Gold(III) compounds have been recognized as anticancer agents due to their structural and electronic similarities with currently employed platinum(II) species. An added benefit to gold(III) agents is the ability to overcome cisplatin resistance. This work identified four gold(III) compounds, [Au(Phen)Cl-2]PF6, [Au(DPQ) Cl-2]PF6, [Au(DPPZ)Cl-2]PF6, and [Au(DPQC)Cl-2]PF6, (Phen = 1,10-phenanthroline, DPQ = dipyrido[3,2d:2',3'-f]quinoxaline. DPPZ = dipyrido[3,2-a:2',3'-c] phenazine, DPQC = dipyrido[3,2-d:2',3'-f] cyclohexyl quinoxaline) that exhibited anticancer activity in both cisplatin sensitive and cisplatin resistant ovarian cancer cells. Two of these compounds, [Au(DPQ)Cl-2]PF6 (AQ) and [Au(DPPZ)Cl-2]PF6 (AZ), displayed exceptional anticancer activity and were the focus of more intensive mechanistic study. At the molecular level, AQand AZ formed DNA adducts, generated free radicals, and upregulated pro-apoptotic signaling molecules (p53, caspases, PARP, death effectors). Taken together, these two novel gold(III) polypyridyl complexes exhibit potent antitumor activity in cisplatin resistant cancer cells. These activities may be mediated, in part, by the activation of apoptotic signaling. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:32 / 42
页数:11
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