Fulda Simone
Institute for Experimental Cancer Research in Pediatrics, Goethe-University Frankfurt, Komturstr. 3a, 60528, Frankfurt, Germany,
Eur J Clin Pharmacol. 2015 May;71(5):525-7. doi: 10.1007/s00228-015-1823-1. Epub 2015 Feb 24.
Targeting the death receptor pathway of apoptosis represents a promising approach for the development of novel cancer therapeutics, since death receptors on the cell surface are directly linked to the apoptotic machinery. The tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) receptor/ligand system is of particular interest among the death receptor superfamily for therapeutic targeting in cancer, since TRAIL has been reported to preferentially induce apoptosis in cancer cells, while sparing non-malignant cells. Evaluation of TRAIL receptor agonists in clinical trials has revealed that they are, in principle, well-tolerated but exert limited efficacy in unselective patient populations. Currently, the challenge resides in the development of rational TRAIL-based combination therapies with potent TRAIL receptor agonists in order to exploit the potential of death receptor targeting for cancer therapy.
靶向细胞凋亡的死亡受体途径是开发新型癌症治疗方法的一种有前景的途径,因为细胞表面的死亡受体与凋亡机制直接相关。肿瘤坏死因子(TNF)相关凋亡诱导配体(TRAIL)受体/配体系统在死亡受体超家族中对于癌症治疗靶向特别受关注,因为据报道TRAIL优先诱导癌细胞凋亡,同时不影响非恶性细胞。在临床试验中对TRAIL受体激动剂的评估表明,原则上它们耐受性良好,但在非选择性患者群体中疗效有限。目前,挑战在于开发合理的基于TRAIL的联合疗法以及有效的TRAIL受体激动剂,以便利用死亡受体靶向治疗癌症的潜力。