Defective cell cycle checkpoints as targets for anti-cancer therapies

被引:62
作者
Gabrielli, Brian [1 ]
Brooks, Kelly [1 ]
Pavey, Sandra [1 ]
机构
[1] Univ Queensland, Princess Alexandra Hosp, Diamantina Inst, Brisbane, Qld 4102, Australia
关键词
checkpoint; targeted therapies; synthetic lethality; DNA-DAMAGE CHECKPOINT; SYNTHETIC LETHALITY; KINASE; CANCER; INHIBITOR; CYTOTOXICITY; CHEMOTHERAPY; PF-00477736; ABROGATION; REGULATOR;
D O I
10.3389/fphar.2012.00009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Conventional chemotherapeutics target the proliferating fraction of cells in the patient's body, which will include the tumor cells, but are also toxic to actively proliferating normal tissues. Cellular stresses, such as those imposed by chemotherapeutic drugs, induce cell cycle checkpoint arrest, and currently approaches targeting these checkpoints are being explored to increase the efficacy and selectivity of conventional chemotherapeutic treatments. Loss of a checkpoint may also make cancer cells more reliant on other mechanisms to compensate for the loss of this function, and these compensatory mechanisms may be targeted using synthetic lethal approaches. Here we will discuss the utility of targeting checkpoint defects as novel anti-cancer therapies.
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页数:6
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