PI3K/AKT/mTOR通路
mTORC2型
mTORC1型
RPTOR公司
蛋白激酶B
激酶
癌症研究
磷脂酰肌醇
化学
药理学
磷酸化
信号转导
生物
生物化学
作者
Dima A. Sabbah,Michael G. Brattain,Haizhen A. Zhong
标识
DOI:10.2174/092986711798347298
摘要
The phosphatidylinositol-3-kinase (PI3K)/AKT/mTOR signaling pathway is a central regulator in cell proliferation, growth, and angiogenesis. Inhibition of this pathway therefore is a major strategy for cancer chemotherapy. In order to induce the maximal therapeutic outcome in cancer treatment, vertical inhibition of the PI3K/AKT/mTOR pathway or horizontal inhibition of PI3K/AKT/mTOR and other kinases has been reported. In this review, we discuss the drug design and clinical development of dual inhibitors of PI3K and mTOR as well as the mTOR-selective inhibitors, classified based on the mechanism of action and the chemical structures. Structural determinants for increasing selectivity toward PI3Kα or mTOR are revealed from the structure-activity relationship of the reported inhibitors. Current clinical development in combination therapy of inhibitors involving in the PI3K/AKT/mTOR pathway is also discussed.
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