Papenfuss Kerstin, Cordier Stefanie M, Walczak Henning
Tumour Immunology Unit, Division of Medicine, Imperial College London, United Kingdom.
J Cell Mol Med. 2008 Dec;12(6B):2566-85. doi: 10.1111/j.1582-4934.2008.00514.x.
Human tumour cells are characterized by their ability to avoid the normal regulatory mechanisms of cell growth, division and death. The classical chemotherapy aims to kill tumour cells by causing DNA damage-induced apoptosis. However, as many tumour cells possess mutations in intracellular apoptosis-sensing molecules like p53, they are not capable of inducing apoptosis on their own and are therefore resistant to chemotherapy. With the discovery of the death receptors the opportunity arose to directly trigger apoptosis from the outside of tumour cells, thereby circumventing chemotherapeutic resistance. Death receptors belong to the tumour necrosis factor receptor superfamily, with tumour necrosis factor (TNF) receptor-1, CD95 and TNF-related apoptosis-inducing ligand-R1 and -R2 being the most prominent members. This review covers the current knowledge about these four death receptors, summarizes pre-clinical approaches engaging these death receptors in anti-cancer therapy and also gives an overview about their application in clinical trials conducted to date.
人类肿瘤细胞的特征在于其能够避开细胞生长、分裂和死亡的正常调节机制。传统化疗旨在通过引起DNA损伤诱导的细胞凋亡来杀死肿瘤细胞。然而,由于许多肿瘤细胞在细胞内凋亡传感分子(如p53)中存在突变,它们无法自行诱导细胞凋亡,因此对化疗具有抗性。随着死亡受体的发现,出现了从肿瘤细胞外部直接触发细胞凋亡的机会,从而规避化疗耐药性。死亡受体属于肿瘤坏死因子受体超家族,其中肿瘤坏死因子(TNF)受体-1、CD95以及TNF相关凋亡诱导配体-R1和-R2是最突出的成员。本综述涵盖了关于这四种死亡受体的当前知识,总结了在抗癌治疗中涉及这些死亡受体的临床前方法,并概述了它们在迄今为止进行的临床试验中的应用。