Targeting the DNA damage response for cancer therapy

被引:66
|
作者
Powell, Simon N. [1 ]
Bindra, Ranjit S. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, New York, NY 10065 USA
关键词
DNA damage response; Double-strand break repair; Single-strand break repair; Homologous recombination; Non-homologous end joining; Checkpoints; Tumor suppressor gene; Chromatin; Hypoxia; Tumor micro-environment; DOUBLE-STRAND BREAK; HISTONE DEACETYLASE INHIBITOR; DEPENDENT PROTEIN-KINASE; INTRACHROMOSOMAL HOMOLOGOUS RECOMBINATION; CAFFEINE-INDUCED RADIOSENSITIZATION; H3; LYSINE-56; ACETYLATION; REPAIR GENE-EXPRESSION; BRCA1 PROMOTER REGION; CELL LUNG-CANCER; MAMMALIAN-CELLS;
D O I
10.1016/j.dnarep.2009.04.011
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Human tumors frequently have defects in the maintenance of genomic integrity, which involve a loss of the appropriate response to DNA damage. These pathways of genome integrity include key proteins involved in cell cycle checkpoints, histone modifications, and DNA repair. In this review, we discuss opportunities for therapeutic intervention by exploiting these defects, with an emphasis on those processes which are primarily associated with the repair of double-strand breaks. As these defects are specific to tumor cells, the development of new anti-cancer agents targeting these pathways may have an enhanced therapeutic window, with limited normal tissue toxicity. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1153 / 1165
页数:13
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