Rowinsky Eric K
ImClone Systems, Branchburg, NJ 08876, USA.
J Clin Oncol. 2005 Dec 20;23(36):9394-407. doi: 10.1200/JCO.2005.02.2889.
Targeted induction of programmed cell death or apoptosis via the extrinsic apoptotic pathway represents an unexploited therapeutic strategy to destroy cancer cells. The activation of cell surface receptors by the tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) results in direct stimulation of apoptotic signaling pathways (extrinsic stimulation). Molecules that directly activate these receptors, such as agonistic monoclonal antibodies to the TRAIL receptors and recombinant TRAIL, are being developed as monotherapies and as part of combination therapies with existing chemotherapeutic drugs and other therapeutic modalities. This article examines the TRAIL receptors as potential targets for activating the TRAIL-mediated apoptosis pathway and presents the current status of novel therapeutics that exploit this pathway, particularly focusing on agonistic monoclonal antibodies to the TRAIL receptors. The preclinical activity, the status of ongoing evaluations, and the potential clinical impact of these novel agents are reviewed.
通过外源性凋亡途径靶向诱导程序性细胞死亡或凋亡是一种尚未得到充分利用的抗癌治疗策略。肿瘤坏死因子相关凋亡诱导配体(TRAIL)激活细胞表面受体可直接刺激凋亡信号通路(外源性刺激)。直接激活这些受体的分子,如TRAIL受体的激动性单克隆抗体和重组TRAIL,正在被开发为单一疗法以及与现有化疗药物和其他治疗方式联合治疗的一部分。本文探讨了TRAIL受体作为激活TRAIL介导的凋亡途径的潜在靶点,并介绍了利用该途径的新型疗法的现状,特别关注TRAIL受体的激动性单克隆抗体。本文还综述了这些新型药物的临床前活性、正在进行的评估情况以及潜在的临床影响。