State Key Laboratory of Genetic Engineering, Institute of Genetics, Fudan University School of Life Sciences, Shanghai, PR China.
Curr Med Chem. 2010;17(29):3309-17. doi: 10.2174/092986710793176285.
Tumor necrosis factor-related apoptosis inducing ligand (TRAIL) is a promising anticancer agent that selectively triggers apoptosis in various cancer cells by interacting with its proapoptotic receptors DR4 and KILLER/DR5. The intensive studies of TRAIL signaling pathways over the past decade have provided clues for understanding the molecular mechanisms of TRAIL-induced apoptosis in carcinogenesis and identified an array of therapeutic responses elicited by TRAIL and its receptor agonists. Preclinical and clinical studies have shown that recombinant TRAIL and the agonistic mono-antibodies targeting TRAIL receptors exhibit potent tumoricidal activities as monotherapies and that the combinatorial therapies of these agents in conjunction with other anticancer modalities such as chemo or radiotherapy amplify the activities of anticancer agents and widen the therapeutic window by overcoming tumor resistance to apoptosis and driving cancer cells to self-destruction. The identification of a number of biomarkers that predict tumor sensitivity of patients to TRAIL-based therapy shed a new light on the personalized therapeutic strategies targeting the TRAIL/TRAIL receptor pathway.
肿瘤坏死因子相关凋亡诱导配体(TRAIL)是一种很有前途的抗癌药物,通过与促凋亡受体 DR4 和 KILLER/DR5 相互作用,选择性地触发各种癌细胞凋亡。在过去十年中对 TRAIL 信号通路的深入研究为理解 TRAIL 诱导的细胞凋亡在致癌作用中的分子机制提供了线索,并确定了 TRAIL 和其受体激动剂引发的一系列治疗反应。临床前和临床研究表明,重组 TRAIL 和针对 TRAIL 受体的单克隆抗体具有作为单一疗法的强大抗肿瘤活性,并且这些药物与其他抗癌方式(如化疗或放疗)联合使用的组合疗法通过克服肿瘤对凋亡的抵抗并促使癌细胞自我毁灭,增强了抗癌药物的活性并拓宽了治疗窗口。许多生物标志物的鉴定表明,患者对基于 TRAIL 的治疗的肿瘤敏感性,为针对 TRAIL/TRAIL 受体途径的个体化治疗策略提供了新的思路。