Regulation of phosphoinositide 3-kinase expression in health and disease

被引:182
|
作者
Kok, Klaartje [1 ,2 ]
Geering, Barbara [3 ]
Vanhaesebroeck, Bart [1 ]
机构
[1] Queen Mary Univ London, Barts & London Sch Med & Dent, Ctr Cell Signalling, Inst Canc, London EC1M 6BQ, England
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Cell Biol, NL-9713 AV Groningen, Netherlands
[3] Univ Bern, Inst Pharmacol, CH-3010 Bern, Switzerland
关键词
ACTIVATED RECEPTOR-GAMMA; HUMAN PHOSPHATIDYLINOSITOL 3-KINASE; INCREASED INSULIN SENSITIVITY; IMPAIRED B-CELL; SKELETAL-MUSCLE; GENE-EXPRESSION; MICE LACKING; ADIPOSE-TISSUE; CATALYTIC SUBUNIT; BINDING-SITE;
D O I
10.1016/j.tibs.2009.01.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Both the biology and the therapeutic potential of the phosphoinositide 3-kinase (PI3K) signalling axis have been the subject of intense investigation; however, little is known about the regulation of PI3K expression. Emerging evidence indicates that PI3K levels change in response to cellular stimulation with insulin and nuclear receptor ligands, and during various physiological and pathological processes including differentiation, regeneration, hypertension and cancer. Recently identified mechanisms that control PI3K production include increased gene copy number in cancer, and transcriptional regulation of the p110 alpha PI3K gene by FOXO3a, NF-kappa B and p53, and of the PI3K regulatory subunits by STAT3, EBNA-2 and SREBP. In most instances, however, the impact of alterations in PI3K expression on PI3K signalling and disease remains to be established.
引用
收藏
页码:115 / 127
页数:13
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