PI3K signalling: the path to discovery and understanding

被引:838
作者
Vanhaesebroeck, Bart [1 ]
Stephens, Len [2 ]
Hawkins, Phillip [2 ]
机构
[1] Univ London, Ctr Cell Signalling, Barts Canc Inst, London EC1M 6BQ, England
[2] Babraham Inst, Inositide Lab, Cambridge CB22 3AT, England
基金
英国生物技术与生命科学研究理事会;
关键词
PROTEIN-KINASE-B; PLECKSTRIN HOMOLOGY DOMAINS; PHOSPHATIDYLINOSITOL 3-KINASE ACTIVATION; HUMAN PHOSPHOINOSITIDE 3-KINASE; GLYCOGEN-SYNTHASE KINASE-3; TUMOR-SUPPRESSOR GENE; PDGF RECEPTOR; 1-PHOSPHATIDYLINOSITOL; 3-KINASE; MEDIATED PHOSPHORYLATION; SELECTIVE INHIBITOR;
D O I
10.1038/nrm3290
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Over the past two decades, our understanding of phospoinositide 3-kinases (PI3Ks) has progressed from the identification of an enzymatic activity associated with growth factors, GPCRs and certain oncogene products to a disease target in cancer and inflammation, with PI3K inhibitors currently in clinical trials. Elucidation of PI3K-dependent networks led to the discovery of the phosphoinositide-binding PH, PX and FYVE domains as conduits of intracellular lipid signalling, the determination of the molecular function of the tumour suppressor PTEN and the identification of AKT and mTOR protein kinases as key regulators of cell growth. Here we look back at the main discoveries that shaped the PI3K field.
引用
收藏
页码:195 / 203
页数:9
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