摘要
细胞周期蛋白依赖性激酶(cyclin-dependent kinase, CDK)4/6通过与细胞周期蛋白D结合,参与DNA的复制和细胞分裂,控制细胞从第一个生长阶段转变至合成阶段,在细胞周期控制中起着关键作用。细胞周期蛋白D-CDK4/6-视网膜母细胞瘤蛋白信号通路的激活有助于肿瘤细胞增殖,因此CDK4/6成为抗肿瘤药物的重要作用靶点之一。本文概要介绍CDK4/6抑制剂的作用机制及其临床研究进展。
Cyclin-dependent kinase(CDK) 4/6 plays a pivotal role in the G1 to S phase of cell cycle by associating with cyclin D, participating in DNA replication and cell division. The activation of cyclin D-CDK4/6-retinoblastoma protein signaling pathway helps tumor cell proliferation, so CDK4/6 has become an important target for clinical treatment of tumors. This article mainly reviews the mechanism of action and clinical research progress of CDK4/6 inhibitors.
作者
张文歆
陈海飞
戚慧洁
王天笑
李群益
ZHANG Wenxin;CHEN Haifei;QI Huijie;WANG Tianxiao;LI Qunyi(Department of Pharmacy,Northern Division of Huashan Hospital,Fudan University,Shanghai 201907,China;Department of Pharmacy,Huashan Hospital,Fudan University,Shanghai 200040,China)
出处
《上海医药》
CAS
2020年第15期13-17,共5页
Shanghai Medical & Pharmaceutical Journal
基金
国家自然科学基金面上项目(81973399)
上海市“医苑新星”青年医学人才培养资助计划(临床药师项目)。