Michael adducts of ascorbic acid as inhibitors of protein phosphatase 2A and inducers of apoptosis

被引:17
作者
Fathi, AR
Krautheim, A
Kaap, S
Eger, K
Steinfelder, HJ
机构
[1] Univ Gottingen, Inst Pharmakol, D-37075 Gottingen, Germany
[2] Univ Leipzig, Inst Pharm, D-04103 Leipzig, Germany
关键词
D O I
10.1016/S0960-894X(00)00294-8
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Michael adducts of ascorbic acid with alpha,beta-unsaturated carbonyl compounds have been shown to be potent inhibitors of protein phosphatase 1 (PPI) without affecting cell viability at the respective concentrations. Here we were able to show that higher concentrations can partially inhibit PP2A activity and concomitantly induce apoptotic cell death. A nitrostyrene adduct of ascorbic acid proved to be a more potent and effective inhibitor of PP2A as well as a stronger inducer of apoptosis. These adducts only slightly lost their cytotoxic potential in multidrug resistant cells that were 10-fold less sensitive to apoptosis induction by okadaic acid and vinblastine. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1605 / 1608
页数:4
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