Division of Hematology and Oncology, Department of Medicine, Indiana University School of Medicine, 840 Westr Walnut St., Indianapolis, IN 46202, USA.
Br J Haematol. 2011 Dec;155(5):561-79. doi: 10.1111/j.1365-2141.2011.08898.x. Epub 2011 Oct 8.
Aurora kinases play an important role in the control of the cell cycle and have been implicated in tumourigenesis in a number of cancers. Among the haematological malignancies, overexpression of Aurora kinases has been reported in acute myeloid leukaemia, chronic myeloid leukaemia, acute lymphoblastic leukaemia, multiple myeloma, aggressive non-Hodgkin lymphoma and Hodgkin lymphoma. A large number of Aurora kinase inhibitors are currently in different stages of clinical development. In addition to varying in their selectivity for the different Aurora kinases, some also have activity directed at other cellular kinases involved in important molecular pathways in cancer cells. This review summarizes the biology of Aurora kinases and discusses why they may be good therapeutic targets in different haematological cancers. We describe preclinical data that has served as the rationale for investigating Aurora kinase inhibitors in different haematological malignancies, and summarize published results from early phase clinical trials. While the anti-tumour effects of Aurora kinase inhibitors appear promising, we highlight important issues for future clinical research and suggest that the optimal use of these inhibitors is likely to be in combination with cytotoxic agents already in use for the treatment of various haematological cancers.
极光激酶在细胞周期的控制中发挥着重要作用,并与多种癌症的肿瘤发生有关。在血液恶性肿瘤中,已经报道在急性髓系白血病、慢性髓系白血病、急性淋巴细胞白血病、多发性骨髓瘤、侵袭性非霍奇金淋巴瘤和霍奇金淋巴瘤中过表达极光激酶。目前有大量的极光激酶抑制剂处于不同的临床开发阶段。除了对不同的极光激酶具有选择性外,一些抑制剂还针对癌细胞中参与重要分子途径的其他细胞激酶具有活性。这篇综述总结了极光激酶的生物学特性,并讨论了它们为什么可能成为不同血液癌症的良好治疗靶点。我们描述了作为在不同血液恶性肿瘤中研究极光激酶抑制剂的基础的临床前数据,并总结了早期临床试验的发表结果。虽然极光激酶抑制剂的抗肿瘤作用很有前景,但我们强调了未来临床研究的重要问题,并建议这些抑制剂的最佳使用可能是与已经用于治疗各种血液癌症的细胞毒性药物联合使用。