Fulda Simone
University Children's Hospital, Eythstr.24, 89075 Ulm, Germany.
Curr Cancer Drug Targets. 2008 Mar;8(2):132-40. doi: 10.2174/156800908783769355.
Triggering apoptosis, the cell's intrinsic death program, is a promising approach for cancer therapy. TNF-related apoptosis-inducing ligand (TRAIL), a member of the TNF superfamily of death inducing ligands, is of special interest for cancer therapy, since TRAIL has been shown to predominantly kill cancer cells, while sparing normal cells. However, since many cancers fail to undergo apoptosis in response to TRAIL treatment, TRAIL-based combination therapies have been developed for cancer-cell specific sensitization towards TRAIL. Chromatin remodelling plays an important role in gene regulation and aberrant architecture of the chromatin has been implicated in tumor formation and progression. In recent years, HDAC inhibitors (HDACI) that reverse aberrant epigenetic changes have emerged as a potential strategy to sensitize cancer cells for TRAIL-induced apoptosis. Synergistic tumor cell death has been reported in a variety of human cancers using different HDACI together with TRAIL. Here, recent advances in the understanding of the molecular events that underlie the synergistic interaction of HDACI and TRAIL are discussed as well as how this knowledge can be translated into the design of cancer-selective novel therapeutics.
触发细胞的内在死亡程序——凋亡,是一种很有前景的癌症治疗方法。肿瘤坏死因子相关凋亡诱导配体(TRAIL)是死亡诱导配体的肿瘤坏死因子超家族成员,因其已被证明主要杀死癌细胞而对正常细胞无损害,故而在癌症治疗中备受关注。然而,由于许多癌症对TRAIL治疗无凋亡反应,基于TRAIL的联合疗法已被开发用于使癌细胞对TRAIL特异性敏感。染色质重塑在基因调控中起重要作用,染色质的异常结构与肿瘤形成和进展有关。近年来,逆转异常表观遗传变化的组蛋白去乙酰化酶抑制剂(HDACi)已成为使癌细胞对TRAIL诱导的凋亡敏感的潜在策略。使用不同的HDACi与TRAIL一起,在多种人类癌症中均报道了协同肿瘤细胞死亡。本文讨论了对HDACi与TRAIL协同相互作用背后分子事件理解的最新进展,以及如何将这些知识转化为癌症选择性新型疗法的设计。