极光抑制剂
极光激酶
胞质分裂
有丝分裂
细胞生物学
极光A激酶
生物
细胞周期
极光激酶B
中心体
蛋白激酶结构域
癌症研究
Polo样激酶
激酶
遗传学
细胞
细胞分裂
基因
突变体
作者
Vassilios Bavetsias,Spiros Linardopoulos
标识
DOI:10.3389/fonc.2015.00278
摘要
The Aurora kinase family comprises of cell cycle-regulated serine/threonine kinases important for mitosis. Their activity and protein expression are cell cycle regulated, peaking during mitosis to orchestrate important mitotic processes including centrosome maturation, chromosome alignment, chromosome segregation, and cytokinesis. In humans, the Aurora kinase family consists of three members; Aurora-A, Aurora-B, and Aurora-C, which each share a conserved C-terminal catalytic domain but differ in their sub-cellular localization, substrate specificity, and function during mitosis. In addition, Aurora-A and Aurora-B have been found to be overexpressed in a wide variety of human tumors. These observations led to a number of programs among academic and pharmaceutical organizations to discovering small molecule Aurora kinase inhibitors as anti-cancer drugs. This review will summarize the known Aurora kinase inhibitors currently in the clinic, and discuss the current and future directions.
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