Targeting the PI3K/AKT/mTOR Signaling Pathway in the Treatment of Human Diseases: Current Status, Trends, and Solutions

被引:75
|
作者
Huang, Jindi [1 ]
Chen, Liye [1 ]
Wu, Jiangxia [1 ]
Ai, Daiqiao [1 ]
Zhang, Ji-Quan [2 ]
Chen, Tie-Gen [3 ]
Wang, Ling [1 ]
机构
[1] Univ Technol, Guangdong Prov Engn & Technol Res Ctr Biopharmaceu, Guangdong Prov Key Lab Fermentat & Enzyme Engn, Sch Biol & Biol Engn,Joint Int Res Lab Synthet Bio, Guangzhou 510006, Peoples R China
[2] Guizhou Med Univ, Coll Pharm, Guiyang 550004, Peoples R China
[3] Chinese Acad Sci, Zhongshan Inst Drug Discovery, Shanghai Inst Mat Med, Zhongshan 528400, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
ADVANCED SOLID TUMORS; 1ST-IN-HUMAN PHASE-I; PHOSPHATIDYLINOSITOL 3-KINASE PI3K; SELECTIVE PI3K-DELTA INHIBITOR; ORALLY BIOAVAILABLE INHIBITOR; RAPAMYCIN KINASE INHIBITOR; ATP-COMPETITIVE INHIBITOR; MAMMALIAN TARGET; HIGHLY POTENT; BIOLOGICAL EVALUATION;
D O I
10.1021/acs.jmedchem.2c01070
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) pathway is one of the most important intracellular pathways involved in cell proliferation, growth, differentiation, and survival. Therefore, this route is a prospective biological target for treating various human diseases, such as tumors, neurodegenerative diseases, pulmonary fibrosis, and diabetes. An increasing number of clinical studies emphasize the necessity of developing novel molecules targeting the PI3K/AKT/mTOR pathway. This review focuses on recent advances in ATP-competitive inhibitors, allosteric inhibitors, covalent inhibitors, and proteolysis-targeting chimeras against the PI3K/AKT/mTOR pathway, and highlights possible solutions for overcoming the toxicities and acquired drug resistance of currently available drugs. We also provide recommendations for the future design and development of promising drugs targeting this pathway.
引用
收藏
页码:16033 / 16061
页数:29
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