Progress in the Preclinical Discovery and Clinical Development of Class I and Dual Class I/IV Phosphoinositide 3-Kinase (PI3K) Inhibitors

被引:0
|
作者
Shuttleworth, S. J. [1 ]
Silva, F. A. [1 ]
Cecil, A. R. L. [1 ]
Tomassi, C. D. [1 ]
Hill, T. J. [1 ]
Raynaud, F. I. [2 ]
Clarke, P. A. [2 ]
Workman, P. [2 ]
机构
[1] Karus Therapeut Ltd, Southampton SO16 7NP, Hants, England
[2] Inst Canc Res, Haddow Labs, Canc Res UK Canc Therapeut Unit, Div Canc Therapeut, Sutton SM2 5NG, Surrey, England
关键词
PI3K; inhibitor; p110; alpha; beta; delta; gamma; mTOR; cancer; inflammation; cardiovascular; BREAST-CANCER; BIOLOGICAL EVALUATION; PI3K/MTOR INHIBITOR; KINASE INHIBITORS; PHOSPHATIDYLINOSITIDE; 3-KINASES; 3-KINASE/MAMMALIAN TARGET; P110-ALPHA INHIBITORS; RHEUMATOID-ARTHRITIS; ANTITUMOR-ACTIVITY; PROTEOMIC ANALYSIS;
D O I
暂无
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
The phosphoinositide 3-kinases (PI3Ks) constitute an important family of lipid kinase enzymes that control a range of cellular processes through their regulation of a network of signal transduction pathways, and have emerged as important therapeutic targets in the context of cancer, inflammation and cardiovascular diseases. Since the mid-late 1990s, considerable progress has been made in the discovery and development of small molecule ATP-competitive PI3K inhibitors, a number of which have entered early phase human trials over recent years from which key clinical results are now being disclosed. This review summarizes progress made to date, primarily on the discovery and characterization of class I and dual class I/IV subtype inhibitors, together with advances that have been made in translational and clinical research, notably in cancer.
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收藏
页码:2686 / 2714
页数:29
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