Cell cycle checkpoint signaling: Cell cycle arrest versus apoptosis

被引:411
作者
Pietenpol, JA [1 ]
Stewart, ZA [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Ctr Mol Toxicol, Dept Biochem, Nashville, TN 37232 USA
关键词
p53; G1; checkpoint; G2; override; cancer; anticancer therapeutics;
D O I
10.1016/S0300-483X(02)00460-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although toxicants may initiate cell damage or stress, the cellular proteins that are involved in control of cell cycle and apoptosis are the final arbiters of cell fate. The biochemical pathways that restrain cell cycle transition and/or induce cell death after stress are known as cell cycle checkpoints. These checkpoints maintain the fidelity of DNA replication, repair, and division. Herein, select cell cycle checkpoint signaling pathways will be discussed and how different components of these pathways are regulated by exogenous and endogenous agents, with focus on the p53 tumor suppressor signaling. The p53 protein is known to play a key role in growth arrest and apoptosis after cell stress, primarily through its ability to regulate the transcription of select downstream target genes in the cell. Further elucidation of the signaling pathways that control growth arrest and apoptosis will continue to provide insights to the complex cellular responses to environmental toxicants. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:475 / 481
页数:7
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