合成致死
效应器
遗传筛选
小型GTPase
生物
突变体
RNA干扰
GTP酶
合成生物学
激酶
基因
计算生物学
癌症研究
遗传学
细胞生物学
信号转导
核糖核酸
出处
期刊:The Enzymes
日期:2013-01-01
卷期号:: 201-219
被引量:8
标识
DOI:10.1016/b978-0-12-420146-0.00009-3
摘要
Mutations in the Ras family of small GTPases are among the most frequent oncogenic events in human cancer. Difficulties in targeting Ras itself and the limited efficacy in targeting its effector kinases have spurred the search for Ras synthetic lethal genes that could shed new light on the biology of Ras-driven cancer and lead to new therapeutic strategies. Advances in mammalian RNAi technology have enabled high-throughput functional screens for Ras synthetic lethal interactions. In this chapter, we summarize the strategies and findings from these screens and discuss future improvement for Ras synthetic lethality studies.
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