Cyclin D3 and c-MYC control glucocorticoid-induced cell cycle arrest but not apoptosis in lymphoblastic leukemia cells

被引:46
作者
Ausserlechner, MJ [1 ]
Obexer, P
Böck, G
Geley, S
Kofler, R
机构
[1] Univ Innsbruck, Sch Med, Inst Pathophysiol, Div Mol Pathophysiol, A-6020 Innsbruck, Austria
[2] Univ Innsbruck, Tyrolean Canc Res Inst, A-6020 Innsbruck, Austria
基金
奥地利科学基金会;
关键词
programmed cell death; dexamethasone; cyclin E; p(27Kip1); Cdk2;
D O I
10.1038/sj.cdd.4401328
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
Glucocorticoids (GC) induce cell cycle arrest and apoptosis in lymphoblastic leukemia cells. To investigate cell cycle effects of GC in the absence of obscuring apoptotic events, we used human CCRF-CEM leukemia cells protected from cell death by transgenic bcl-2. GC treatment arrested these cells in the G1 phase of the cell cycle due to repression of cyclin D3 and c-myc. Cyclin E and Cdk2 protein levels remained high, but the kinase complex was inactive due to increased levels of bound p27(Kip1). Conditional expression of cyclin D3 and/or c-myc was sufficient to prevent GC-induced G1 arrest and p27(Kip1) accumulation but, importantly, did not interfere with the induction of apoptosis. The combined data suggest that repression of both, c-myc and cyclin D3, is necessary to arrest human leukemia cells in the G1 phase of the cell division cycle, but that neither one is required for GC-induced apoptosis.
引用
收藏
页码:165 / 174
页数:10
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