INACTIVATION OF CDC2 INCREASES THE LEVEL OF APOPTOSIS INDUCED BY DNA-DAMAGE

被引:0
|
作者
ONGKEKO, W
FERGUSON, DJP
HARRIS, AL
NORBURY, C
机构
[1] UNIV OXFORD, INST MOLEC MED, IMPERIAL CANC RES FUND, MOLEC ONCOL LAB, OXFORD OX3 9DU, ENGLAND
[2] JOHN RADCLIFFE HOSP, NUFFIELD DEPT PATHOL, OXFORD OX3 9DU, ENGLAND
基金
英国惠康基金;
关键词
APOPTOSIS; CDC2; CELL CYCLE; CHECKPOINT; MITOXANTRONE; OLOMOUCINE;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A number of lines of evidence have suggested a possible involvement of the mitosis-promoting protein kinase Cdc2 in the process of apoptotic cell death, and one recent study concluded that premature activation of Cdc2 is required for apoptosis. Here we have used a temperature-sensitive murine Cdc2 mutant cell line and Cdc2 inhibitor compounds to study the effect of inhibition of this protein kinase on apoptosis induced by DNA-damaging drugs. Inhibition of Cdc2 activity before or during exposure to DNA strand break-inducing drugs had the effect of increasing the level of subsequent apoptosis, as assessed by electron microscopy and flow cytometry. We conclude that, far from being required for cell death, a form of mammalian Cdc2 suppresses apoptosis induced by DNA damage. This form of Cdc2 appears to be active in G(2)-arrested cells and is therefore presumably distinct from the mitosis-promoting Cdc2-cyclin B heterodimer.
引用
收藏
页码:2897 / 2904
页数:8
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