Hsp90 inhibitors identified from a library of novobiocin analogues

被引:162
作者
Yu, XM
Shen, G
Neckers, L
Blake, H
Holzbeierlein, J
Cronk, B
Blagg, BSJ
机构
[1] Univ Kansas, Dept Med Chem, Lawrence, KS 66045 USA
[2] Univ Kansas, Ctr Prot Struct & Funct, Lawrence, KS 66045 USA
[3] NCI, Urol Oncol Branch, NIH, Rockville, MD 20850 USA
[4] Univ Kansas, Med Ctr, Dept Urol, Kansas City, KS 66103 USA
关键词
D O I
10.1021/ja0535864
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Novobiocin is a C-terminal inhibitor of the Hsp90 protein folding machinery, which is responsible for the conformational maturation of numerous proteins involved in cancer growth and survival. Due to novobiocin's poor inhibitory activity (∼700 μM), very little attention has been paid toward the development of novobiocin analogues for Hsp90 inhibition. In this study, a parallel library of 20 novobiocin derivatives was prepared and the biological activity of each evaluated by Western blot analysis of Hsp90 client proteins. A4 was found to be a potent inhibitor of Hsp90 as determined by its ability to cause the degradation of several Hsp90 client proteins in both breast and prostate cancer cell lines. In the presence of 1 μM A4, several Hsp90 client proteins were degraded, including AKT, Her2, Hif-1α, and the androgen receptor. Copyright © 2005 American Chemical Society.
引用
收藏
页码:12778 / 12779
页数:2
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