PI3K/AKT/mTOR通路
蛋白激酶B
药物开发
药物发现
信号转导
药理学
临床试验
癌症研究
药品
计算生物学
生物信息学
生物
细胞生物学
作者
Dima A. Sabbah,Rima Hajjo,Sanaa K. Bardaweel,Haizhen A. Zhong
标识
DOI:10.1080/13543776.2024.2338100
摘要
Introduction Recent years have witnessed great achievements in drug design and development targeting the phosphatidylinositol 3-kinase/protein kinase-B (PI3K/AKT) signaling pathway, a pathway central to cell growth and proliferation. The nearest neighbor protein-protein interaction networks for PI3K and AKT show the interplays between these target proteins which can be harnessed for drug discovery. In this review, we discuss the drug design and clinical development of inhibitors of PI3K/AKT in the past three years. We review in detail the structures, selectivity, efficacy, and combination therapy of thirty-five inhibitors targeting these proteins, classified based on the target proteins. Approaches to overcoming drug resistance and to minimizing toxicities are discussed. Future research directions for developing combinational therapy and PROTACs of PI3K and AKT inhibitors are also discussed.
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