细胞周期蛋白依赖激酶5
细胞周期蛋白依赖激酶
化学
药物发现
药物开发
临床试验
激酶
药理学
药品
蛋白激酶A
生物信息学
细胞周期
细胞周期蛋白依赖激酶2
生物化学
医学
细胞
生物
作者
Wentao Tang,Congcong Lin,Quanwei Yu,Dan Zhang,Yun Liu,Lele Zhang,Zhilan Zhou,Jifa Zhang,Liang Ouyang
标识
DOI:10.1021/acs.jmedchem.3c00566
摘要
Cyclin-dependent kinase 5 (CDK5) protein plays an important role not only in the central nervous system but also in the periphery, including immune response, regulation of insulin secretion, and cancer development and progression. Consequently, targeting the CDK5 protein is a potential strategy for the treatment of many diseases, especially cancer and neurodegenerative diseases. To date, numerous pan-CDK inhibitors have entered clinical trials. Nevertheless, limited clinical efficacy and severe adverse effects have prompted the application of new techniques to optimize clinical efficacy and minimize adverse events. In this Perspective, we highlight the protein properties, biofunctions, relevant signaling pathways, and associations with cancer development and proliferation of CDK5, and analyze the clinical status of pan-CDK inhibitors and the preclinical status of CDK5-specific inhibitors. In addition, CDK5-selective inhibitors, protein–protein interaction inhibitors, proteolytic-targeting chimera (PROTAC) degraders, and dual-target CDK5 inhibitors are discussed.
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