Synthetic lethality and cancer

被引:0
作者
Nigel J. O'Neil
Melanie L. Bailey
Philip Hieter
机构
[1] Michael Smith Laboratories,
[2] University of British Columbia,undefined
来源
Nature Reviews Genetics | 2017年 / 18卷
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摘要
Synthetic lethal genetic interactions with tumour-specific mutations may be exploited to develop anticancer therapeutics.Synthetic dosage lethality and conditional synthetic lethality can expand the scope of conventional synthetic lethal studies.Genetic interaction networks in model organisms provide a framework for screening cancer-relevant candidate synthetic lethal interactions in human cells.Large-scale screening for cancer gene-specific synthetic lethal candidates in human cells has progressed through advances in RNA interference and the CRISPR–Cas9 system.The CRISPR–Cas9 technology is a versatile platform for exploring genetic networks and synthetic lethal interaction phenotypes.The search for synthetic lethality-based therapeutic strategies could be enhanced by integrating synthetic lethal interactions from three distinct sources: model organism genetic networks, human high-throughput screening and synthetic lethal predictions from statistical genetics.
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页码:613 / 623
页数:10
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