The DNA damage-induced cell death response: a roadmap to kill cancer cells

被引:221
作者
Matt, Sonja [1 ]
Hofmann, Thomas G. [1 ]
机构
[1] DKFZ ZMBH Alliance, German Canc Res Ctr Dkfz, Cellular Senescence Grp, Neuenheimer Feld 280, D-69120 Heidelberg, Germany
关键词
Adriamycin; ATM; ATR; Axin; c-Abl; BAX; Cancer therapy; Caspase; 2; Chk1; Chk2; Doxorubicin; FOXO3; HIPK2; Hippo pathway; Ionizing radiation; Yap1; MLKL; p53; Serine; 46; p73; PML; PIDD; Pin1; PUMA; RIPK1; RIPK3; SUMO; XAF1; NF-KAPPA-B; INTERACTING PROTEIN KINASE-2; DOUBLE-STRAND BREAKS; PROLYL-ISOMERASE PIN1; MITOCHONDRIAL PERMEABILITY TRANSITION; OUTER-MEMBRANE PERMEABILIZATION; C-ABL; GENOTOXIC STRESS; APOPTOTIC RESPONSE; P53-DEPENDENT APOPTOSIS;
D O I
10.1007/s00018-016-2130-4
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
Upon massive DNA damage cells fail to undergo productive DNA repair and trigger the cell death response. Resistance to cell death is linked to cellular transformation and carcinogenesis as well as radio- and chemoresistance, making the underlying signaling pathways a promising target for therapeutic intervention. Diverse DNA damage-induced cell death pathways are operative in mammalian cells and finally culminate in the induction of programmed cell death via activation of apoptosis or necroptosis. These signaling routes affect nuclear, mitochondria- and plasma membrane-associated key molecules to activate the apoptotic or necroptotic response. In this review, we highlight the main signaling pathways, molecular players and mechanisms guiding the DNA damage-induced cell death response.
引用
收藏
页码:2829 / 2850
页数:22
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