Apoptosis and autophagy: Regulation of apoptosis by DNA damage signalling - roles of p53, p73 and HIPK2

被引:80
作者
Bitomsky, Nadja [1 ]
Hofmann, Thomas G. [1 ]
机构
[1] DKFZ ZMBH Alliance, German Canc Res Ctr, Cellular Senescence Grp A210, D-69120 Heidelberg, Germany
关键词
apoptosis; ataxia-telangiectasia mutated (ATM); ataxia-telangiectasia mutated and Rad3-related (ATR); DNA damage; homeodomain-interacting protein kinase 2 (HIPK2); nuclear bodies; p53; p73; promyelocytic leukaemia (PML); HOMEODOMAIN-INTERACTING PROTEIN-KINASE-2; DOUBLE-STRAND BREAKS; C-ABL; P53-DEPENDENT APOPTOSIS; PROTEIN KINASE-2; NUCLEAR-BODIES; DEPENDENT PHOSPHORYLATION; SELECTIVE ACTIVATION; JNK PHOSPHORYLATION; MEDIATES APOPTOSIS;
D O I
10.1111/j.1742-4658.2009.07331.x
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
Genomic stability is constantly threatened by DNA damage, caused by numerous environmental and intrinsic sources, including radiation, chemicals and oncogene expression. Consequently, cells have evolved a sophisticated signal transduction network to sense DNA damage and to mount an appropriate DNA damage response. Dysregulation of the DNA damage response leads to genomic instability and cancer. Dependent on the cellular background and extent of DNA damage, the DNA damage response triggers cell cycle arrest and DNA repair, or in the case of irreparable damage, inactivation of the cells by senescence or apoptosis. In this minireview, we concentrate on the apoptotic response to DNA damage and signalling pathways linked to the cell nucleus and nuclear bodies, with a particular focus on the molecular players p53 and p73 and on the DNA damage-activated kinase homeodomain-interacting protein kinase 2 (HIPK2).
引用
收藏
页码:6074 / 6083
页数:10
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