Targeting cancer cells by synthetic lethality

被引:23
作者
Chan, Denise A. [1 ]
Giaccia, Amato J. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Radiat Oncol, Div Radiat & Canc Biol, Stanford, CA 94305 USA
关键词
drug discovery; hypoxia; renal cell carcinoma; synthetic lethality; targeted therapy; von Hippel-Lindau;
D O I
10.4161/cc.7.19.6776
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Standard cytotoxic agents for treating cancer were developed based on their effectiveness to kill rapidly dividing cells, not on their ability to selectively kill cancer cells and spare normal tissue. Much of contemporary cancer research is aimed at identifying specific molecular features of cancers to directly target tumor cells with the hope of reducing or eliminating unwanted side effects. Targeted therapy for the treatment of cancer can be divided into two main categories: monoclonal antibodies and small molecules. In this Perspective, we review the approach of synthetic lethality to target cancer, specifically renal cell carcinoma. The concept of synthetic lethality is used to describe a genetic interaction of two non-allelic and non-lethal genes that when mutated simultaneously results in cell death. Recently, we identified a compound, STF-62247, that functions in a synthetic lethal manner to the loss of VHL, a mutation found in the majority of renal cell carcinomas.
引用
收藏
页码:2987 / 2990
页数:4
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