极光抑制剂
极光激酶B
生物
极光激酶
极光A激酶
有丝分裂
激酶
磷酸化
细胞生物学
主轴检查点
癌症研究
组蛋白H3
主轴装置
细胞凋亡
癌细胞
乙酰化
细胞周期
生物化学
细胞
癌症
细胞分裂
遗传学
基因
作者
Rebecca K. Tyler,Natalia Shpiro,Rodolfo Márquez,Patrick A. Eyers
出处
期刊:Cell Cycle
[Taylor & Francis]
日期:2007-11-15
卷期号:6 (22): 2846-2854
被引量:118
摘要
VX-680, also known as MK-0457, is a member of a diverse group of small molecules that inhibit the Aurora kinases, and has shown significant potential as an anti-cancer agent. In keeping with many protein kinase inhibitors, this compound is not a monospecific agent, and its cellular specificity remains largely unknown. In cells, VX-680 blocks mitotic Histone H3 phosphorylation and induces polyploidy and apoptosis, consistent with inhibition of the mitotic protein kinase Aurora B. In this study, we have investigated the effects of VX-680 in proliferating human cancer cells, and demonstrate that it blocks the phosphorylation and activation of both Aurora A and B. Additionally, VX-680 suppresses the phosphorylation of specific substrates of each enzyme, including the Aurora A target TACC3 on Ser558. Exposure to VX-680 induces a monopolar spindle phenotype, delays mitotic progression and rapidly overrides the spindle assembly checkpoint in the presence of spindle poisons. VX-680 also exhibits potent cytotoxicity when compared to the well documented Aurora B inhibitor ZM447439. Taken together, these data identify Aurora A and Aurora B as dual intracellular targets of VX-680.
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