Targeting heat-shock-protein 90 (Hsp90) by natural products: geldanamycin, a show case in cancer therapy

被引:70
作者
Franke, Jana [1 ,2 ]
Eichner, Simone [1 ,2 ]
Zeilinger, Carsten [3 ]
Kirschning, Andreas [1 ,2 ]
机构
[1] Leibniz Univ Hannover, Inst Organ Chem, D-30167 Hannover, Germany
[2] Leibniz Univ Hannover, Zentrum Biomol Wirkstoffchem BMWZ, D-30167 Hannover, Germany
[3] Leibniz Univ Hannover, Inst Biophys, D-30419 Hannover, Germany
关键词
ENZYME-SPECIFIC ACTIVATION; ATP-BINDING DOMAIN; MOLECULAR CHAPERONE; CRYSTAL-STRUCTURE; IN-VIVO; TRANSCRIPTIONAL ACTIVITY; CONFORMATIONAL DYNAMICS; PLASMODIUM-FALCIPARUM; BIOLOGICAL EVALUATION; STRUCTURAL DIVERSITY;
D O I
10.1039/c3np70012g
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
In this review recent progress in the development of heat shock proteins (Hsp90) in oncogenesis is illuminated. Particular emphasis is put on inhibitors such as geldanamycin and analogues that serve as a natural product show case. Hsp90 has emerged as an important target in cancer therapy and/or against pathogenic cells which elicit abnormal Hsp patterns. Competition for ATP by geldanamycin and related compounds abrogate the chaperone function of Hsp90. In this context, this account pursues three topics in detail: a) Hsp90 and its biochemistry, b) Hsp90 and its role in oncogenesis and c) strategies to create compound libraries of structurally complex inhibitors like geldanamycin on which SAR studies and the development of drugs that are currently in different stages of clinical testing rely.
引用
收藏
页码:1299 / 1323
页数:25
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