新生霉素
热休克蛋白90
化学
雄激素受体
生物化学
癌症
前列腺癌
热休克蛋白
生物
基因
遗传学
抗生素
作者
Xiao Yu,Gang Shen,Len Neckers,Helen M. Blake,Jeff M. Holzbeierlein,Benjamin Cronk,Brian S. J. Blagg
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 ( approximately 700 muM), 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 muM A4, several Hsp90 client proteins were degraded, including AKT, Her2, Hif-1alpha, and the androgen receptor.
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