Molecular targeting of Gα and Gβγ subunits: a potential approach for cancer therapeutics

被引:54
作者
Smrcka, Alan V. [1 ]
机构
[1] Univ Rochester, Dept Physiol & Pharmacol, Sch Med & Dent, Rochester, NY 14627 USA
关键词
COUPLED RECEPTOR KINASE-2; PROTEIN SIGNALING RGS; CRYSTAL-STRUCTURE; DRUG DISCOVERY; MUTATIONS; RECOGNITION; REGULATORS; INHIBITOR; GENE; DISRUPTION;
D O I
10.1016/j.tips.2013.02.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
G-Protein-coupled receptors (GPCRs) signal through G protein alpha and beta gamma subunit families to regulate a wide range of physiological and pathophysiological processes. As such, GPCRs are major targets for therapeutic drugs. Downstream targets of GPCRs have also gained interest as a therapeutic approach to complex pathologies involving multiple GPCRs. One such approach involves targeting of the G proteins themselves. Several small molecule G alpha and G beta gamma modulators have been developed and been tested in various animal models of disease. Here we will discuss the requirements for targeting G alpha and G beta gamma subunits, the mechanisms of action of currently identified inhibitors, and focus on the potential utility of G alpha and G beta gamma inhibitors in the treatment of various cancers.
引用
收藏
页码:290 / 298
页数:9
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