Mater Research Institute, The University of Queensland, Brisbane, Queensland, Australia.
The University of Queensland Diamantina Institute, Translational Research Institute, Brisbane, Queensland, Australia.
Mol Cancer Ther. 2017 Sep;16(9):1934-1941. doi: 10.1158/1535-7163.MCT-17-0159. Epub 2017 May 18.
The activity and efficacy of Aurora inhibitors have been reported in a wide range of cancer types. The most prominent Aurora inhibitor is alisertib, an investigational Aurora inhibitor that has been the subject of more than 30 clinical trials. Alisertib has inhibitory activity against both Aurora A and B, although it is considered to be primarily an Aurora A inhibitor Here, we show that alisertib inhibits both Aurora A and B in preclinical models of HPV-driven cervical cancer, and that it is the inhibition of Aurora A and B that provides the selectivity and efficacy of this drug in this disease setting. We also present formal evidence that alisertib requires progression through mitosis for its efficacy, and that it is unlikely to combine with drugs that promote a G DNA damage checkpoint response. This work demonstrates that inhibition of Aurora A and B is required for effective control of HPV-driven cancers by Aurora kinase inhibitors. .
极光激酶抑制剂在多种癌症类型中的活性和疗效已有报道。最突出的极光激酶抑制剂是alisertib,一种研究中的极光激酶抑制剂,已经进行了 30 多项临床试验。Alisertib 对 Aurora A 和 B 都有抑制作用,尽管它被认为主要是 Aurora A 抑制剂。在这里,我们表明 alisertib 抑制 HPV 驱动的宫颈癌的临床前模型中的 Aurora A 和 B,并且抑制 Aurora A 和 B 为这种药物在这种疾病环境中的选择性和疗效提供了依据。我们还提供了正式的证据表明,alisertib 需要通过有丝分裂才能发挥其疗效,而且它不太可能与促进 G 期 DNA 损伤检查点反应的药物结合。这项工作表明,抑制 Aurora A 和 B 是 Aurora 激酶抑制剂有效控制 HPV 驱动型癌症所必需的。