PI3K/Akt/mTOR inhibitors in cancer: At the bench and bedside

被引:697
|
作者
Alzahrani, Ali S. [1 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Div Mol Endocrinol, Dept Mol Oncol, POB 3354,Res Ctr MBC 03, Riyadh 11211, Saudi Arabia
关键词
PI3K; Akt; mTOR; Cancer; Inhibitors; PHASE-II TRIAL; AKT INHIBITOR; AROMATASE INHIBITORS; SELECTIVE INHIBITOR; ACQUIRED-RESISTANCE; MTOR INHIBITORS; PI3K PATHWAY; COMBINATION; MUTATIONS; RAPAMYCIN;
D O I
10.1016/j.semcancer.2019.07.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Phosphatidylinositol 3-kinase (PI3K)/Akt/mammalian target of rapamycin (mTOR) signaling pathway is one of the major cellular signaling pathways that plays an important role in basic intracellular functions. The PI3K/ Akt/mTOR pathway regulates cell proliferation, growth, cell size, metabolism, and motility. Component genes of this pathway have been extensively studied and found to be commonly activated in human cancer. Inhibition of this pathway has been shown to lead to regression of human tumors and has been studied in preclinical setup and evaluated in many clinical trials at various levels. Some inhibitors of this pathway are approved by the Food and Drug Administration after their potency and safety have been shown in clinical trials. This review discusses the recent trends in exploiting the PI3K/Akt/mTOR pathway towards the molecular targeted therapy using small molecule inhibitors in human cancer.
引用
收藏
页码:125 / 132
页数:8
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