医学
极光激酶
极光抑制剂
激酶
极光激酶B
临床试验
极光A激酶
肿瘤科
癌症
内科学
癌症研究
细胞周期
生物
基因
动细胞
细胞生物学
生物化学
染色体
化学
作者
Gerald S. Falchook,Christel C. Bastida,Razelle Kurzrock
标识
DOI:10.1053/j.seminoncol.2015.09.022
摘要
The Aurora kinase family of kinases (Aurora A, B, and C) are involved in multiple mitotic events, and aberrant expression of these kinases is associated with tumorigenesis. Aurora A and Aurora B are validated anticancer targets, and the development of Aurora kinase inhibitors has progressed from preclinical to clinical studies. A variety of Aurora A, B and pan-Aurora kinase inhibitors have entered the clinic. The main side effects include febrile neutropenia, stomatitis, gastrointestinal toxicity, hypertension, and fatigue. Responses including complete remissions have been described in diverse, advanced malignancies, most notably ovarian cancer and acute myelogenous leukemia. This review highlights the biologic rationale for Aurora kinase as a target, and clinical trials involving Aurora kinase inhibitors, with particular emphasis on published early phase studies, and the observed anti-tumor activity of these agents.
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