Limami Y, Pinon A, Riaz A, Simon A
Faculté de Pharmacie EA 1069 Laboratoire de Chimie des Substances Naturelles Limoges France limami@hotmail.com.
Faculté de Pharmacie EA 1069 Laboratoire de Chimie des Substances Naturelles Limoges France.
Cell Mol Biol (Noisy-le-grand). 2015 Oct 30;61(6):33-8.
Targeting cancer cells is one of the challenges of current treatment strategies. TRAIL represents a promising therapeutic approach and over the past decades there was an increased interest in targeting TRAIL signaling to treat cancer. Indeed, TRAIL can specifically target cancer cells and exhibits very low cytotoxicity towards normal cells. However, rapidly accumulating experimental evidence has started to shed light on multiple factors which induce resistance against TRAIL in cancer cells. This resistance consists of various mechanisms including downregulation of death receptors and caspase-8 and overexpression of decoy receptors as well as antiapoptotic factors such as members of Bcl-2 family. Even if several studies focused on elucidating those resistance mechanisms, there still remain gray areas that need to be fully elucidated. Thus, therapeutic approaches could consist of targeting both resistance signaling pathways and TRAIL signaling to enhance TRAIL therapy efficiency.
靶向癌细胞是当前治疗策略面临的挑战之一。肿瘤坏死因子相关凋亡诱导配体(TRAIL)是一种很有前景的治疗方法,在过去几十年里,人们对靶向TRAIL信号通路治疗癌症的兴趣与日俱增。事实上,TRAIL可以特异性地靶向癌细胞,并且对正常细胞表现出极低的细胞毒性。然而,迅速积累的实验证据开始揭示多种导致癌细胞对TRAIL产生抗性的因素。这种抗性由多种机制组成,包括死亡受体和半胱天冬酶-8的下调、诱饵受体的过表达以及抗凋亡因子(如Bcl-2家族成员)的过表达。即使有几项研究专注于阐明这些抗性机制,但仍存在一些需要充分阐明的灰色地带。因此,治疗方法可以包括靶向抗性信号通路和TRAIL信号通路,以提高TRAIL治疗的效率。