[Au2(phen2Me)2(μ-O)2](PF6)2, a Novel Dinuclear Gold(III) Complex Showing Excellent Antiproliferative Properties

被引:75
|
作者
Cinellu, Maria A. [1 ]
Maiore, Laura [1 ]
Manassero, Mario [2 ]
Casini, Angela [3 ]
Arca, Massimiliano [4 ]
Fiebig, Heinz-Herbert [5 ]
Kelter, Gerhard [5 ]
Michelucci, Elena [6 ]
Pieraccini, Giuseppe [6 ]
Gabbiani, Chiara [7 ]
Messori, Luigi [7 ]
机构
[1] Univ Sassari, Dept Chem, I-07100 Sassari, Italy
[2] Univ Milan, Dept Struct Chem & Inorgan Stereochem, I-20133 Milan, Italy
[3] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
[4] Univ Cagliari, Dept Inorgan & Analyt Chem, I-09042 Monserrato, CA, Italy
[5] Oncotest GmbH, Inst Expt Oncol, D-79108 Freiburg, Germany
[6] Univ Florence, Mass Spectrometry Ctr CISM, I-50019 Florence, Italy
[7] Univ Florence, Dept Chem Ugo Schiff, I-50019 Florence, Italy
来源
ACS MEDICINAL CHEMISTRY LETTERS | 2010年 / 1卷 / 07期
基金
瑞士国家科学基金会;
关键词
Cytotoxic gold compounds; COMPARE analysis; protein targets; anticancer agents; ANTICANCER AGENTS; PROTEIN INTERACTIONS; SOLUTION CHEMISTRY; DRUGS; CISPLATIN; DNA;
D O I
10.1021/ml100097f
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A novel dioxo-bridged dinuclear gold(III) complex with two 2,9-dimethylphenanthroline ligands was synthesized and thoroughly characterized. Its crystal structure was solved, and its solution behavior assessed. Remarkably, this compound revealed excellent antiproliferative properties in vitro against a wide panel of 36 cancer cell lines, combining a high cytotoxic potency to pronounced tumor selectivity. Very likely, these properties arise from an innovative mode of action (possibly involving histone deacetylase inhibition), as suggested by COMPARE analysis. In turn, electrospray ionization-mass spectrometry studies provided valuable insight into its molecular mechanisms of activation and of interaction with protein targets. Gold (III) reduction, dioxo bridge-disruption, coordinative gold(I) binding to the protein, and concomitant release of the phenanthroline ligand were proposed to occur upon interaction with superoxide dismutase, used here as a model protein. Because of the reported results, this new gold(III) compund qualifies itself as an optimal candidate for further pharmocological testing.
引用
收藏
页码:336 / 339
页数:4
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