DNA damage signalling and NF-κB:: implications for survival and death in mammalian cells

被引:17
作者
Boland, MP [1 ]
机构
[1] Univ Cambridge, Dept Pathol, Cambridge CB2 1QP, England
关键词
apoptosis; ataxia telangiectasia mutated; checkpoint; DNA damage repair; p53; signal transducer and activator of transcription;
D O I
10.1042/0300-5127:0290674
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
Nuclear factor kappaB (NF-kappaB), p53 and signal transducer and activator of transcription (STAT) proteins are transcription factors that are known to regulate cell fate in response to apoptotic stimuli. They may, therefore, represent components of drug responses that determine drug efficacy. This review will describe data illustrating some recent progress in our understanding of the mechanism of NF-KB activation after treatment of cells with DNA-damaging anti-cancer drugs. Furthermore, it will discuss how this and other transcriptional events, including STAT transcription factor activation, may effect the promotion or attenuation of apoptosis in target cells. In this regard, certain STAT family members may lie downstream of signalling pathways that are activated after DNA damage. Finally, it will be discussed how proteins normally linked with DNA damage signalling such as p53 may be regulated in response to physiological signals, revealing their role in developmental checkpoints such as differentiation commitment.
引用
收藏
页码:674 / 678
页数:5
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