Glycogen synthase kinase-3 (GSK-3) inhibition induces apoptosis in leukemic cells through mitochondria-dependent pathway

被引:30
|
作者
Mirlashari, Mohammad Reza [1 ]
Randen, Ingrid [1 ,2 ]
Kjeldsen-Kragh, Jens [1 ,2 ]
机构
[1] Oslo Univ Hosp, Dept Immunol & Transfus Med, N-0407 Oslo, Norway
[2] Univ Oslo, Inst Clin Med, Oslo, Norway
关键词
Glycogen synthase kinase-3; Leukemia; Apoptosis; Mitochondria membrane potential; beta-Catenin; SMALL-MOLECULE INHIBITORS; DRUG-INDUCED APOPTOSIS; COLON-CANCER CELLS; BETA-CATENIN; NEURONAL APOPTOSIS; GENE-TRANSCRIPTION; CASPASE ACTIVATION; DNA-DAMAGE; LITHIUM; EXPRESSION;
D O I
10.1016/j.leukres.2011.11.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The roles of glycogen synthase kinase-3 (GSK-3) in cell survival and apoptosis are controversial. We examined the effect of a specific GSK-3 inhibitor (SB-415286) on the regulation of leukemic cells proliferation and apoptosis. SB-415286 (40 mu M) induced cell growth inhibition, beta-catenin stabilization, cell cycle arrest in G(2)/M phase, cyclin B1 downregulation, and apoptosis in leukemic cell lines KG1a, K562, and CMK. Blocking the death receptor pathway by using a specific inhibitor of caspase-8, did not inhibit SB-415286-induced apoptosis. This indicates that activation of caspase-8 is part of the intrinsic apoptotic pathway and occurs downstream of mitochondria membrane potential depolarization mediated by other caspases. Furthermore, we found that depolarization of mitochondria membrane caused by GSK-3 inhibition is regulated by dephosphorylation of anti-apoptotic protein Bcl-2 and downregulation of Bcl-xL. Thus, inhibition of GSK-3-induced apoptosis of leukemic cells could be an attractive target for treatment of leukemia. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:499 / 508
页数:10
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