Yap Timothy A, Garrett Michelle D, Walton Mike I, Raynaud Florence, de Bono Johann S, Workman Paul
Cancer Research UK Centre for Cancer Therapeutics, The Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey, UK.
Curr Opin Pharmacol. 2008 Aug;8(4):393-412. doi: 10.1016/j.coph.2008.08.004. Epub 2008 Aug 27.
The strategy of 'drugging the cancer kinome' has led to the successful development and regulatory approval of several novel molecular targeted agents. The spotlight is now shifting to the phosphatidylinositide 3-kinase (PI3K)-AKT-mammalian target of rapamycin (mTOR) pathway as a key potential target. This review details the role of the pathway in oncogenesis and the rationale for inhibiting its vital components. The focus will be on the progress made in the development of novel therapies for cancer treatment, with emphasis placed on agents that have entered clinical development. Strategies involving horizontal and vertical blockade of the pathway, as well as the use of biomarkers to select appropriate patients and to provide proof of target modulation will also be highlighted. Finally, we discuss the issues and limitations involved with targeting the PI3K-AKT-mTOR pathway, and predict what the future may hold for these novel anticancer therapeutics.
“针对癌症激酶组用药”策略已促成了几种新型分子靶向药物的成功研发及监管批准。目前,聚磷脂酰肌醇3激酶(PI3K)-AKT-雷帕霉素哺乳动物靶点(mTOR)信号通路作为一个关键潜在靶点备受关注。本综述详细阐述了该信号通路在肿瘤发生中的作用以及抑制其关键组分的理论依据。重点将放在癌症治疗新型疗法的研发进展上,尤其侧重于已进入临床开发阶段的药物。还将突出涉及该信号通路横向和纵向阻断的策略,以及利用生物标志物来选择合适患者并提供靶点调控证据的方法。最后,我们将讨论靶向PI3K-AKT-mTOR信号通路所涉及的问题和局限性,并预测这些新型抗癌疗法的未来发展前景。