DNA repair dysregulation from cancer driver to therapeutic target

被引:927
作者
Curtin, Nicola J. [1 ]
机构
[1] Newcastle Univ, No Inst Canc Res, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
基金
英国工程与自然科学研究理事会;
关键词
DEPENDENT PROTEIN-KINASE; DOUBLE-STRAND BREAKS; BASE EXCISION-REPAIR; HOMOLOGOUS RECOMBINATION REPAIR; POLY(ADP-RIBOSE) POLYMERASE INHIBITOR; SMALL-MOLECULE INHIBITOR; REFRACTORY SOLID TUMORS; CROSS-LINK REPAIR; MISMATCH-REPAIR; PHASE-I;
D O I
10.1038/nrc3399
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Dysregulation of DNA damage repair and signalling to cell cycle checkpoints, known as the DNA damage response (DDR), is associated with a predisposition to cancer and affects responses to DNA-damaging anticancer therapy. Dysfunction of one DNA repair pathway may be compensated for by the function of another compensatory DDR pathway, which may be increased and contribute to resistance to DNA-damaging chemotherapy and radiotherapy. Therefore, DDR pathways make an ideal target for therapeutic intervention; first, to prevent or reverse therapy resistance; and second, using a synthetic lethal approach to specifically kill cancer cells that are dependent on a compensatory DNA repair pathway for survival in the context of cancer-associated oxidative and replicative stress. These hypotheses are currently being tested in the laboratory and are being translated into clinical studies
引用
收藏
页码:801 / 817
页数:17
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