Almasan Alexandru, Ashkenazi Avi
Department of Cancer Biology, Lerner Research Institute, The Cleveland Clinic Foundation, Cleveland, OH 44195, USA.
Cytokine Growth Factor Rev. 2003 Jun-Aug;14(3-4):337-48. doi: 10.1016/s1359-6101(03)00029-7.
Apo2 ligand or tumor necrosis factor (TNF)-related apoptosis-inducing ligand (Apo2L/TRAIL) is one of several members of the TNF gene superfamily that induce apoptosis through engagement of death receptors. Apo2L/TRAIL is unusual as compared to any other cytokine as it interacts with a complex system of receptors: two pro-apoptotic death receptors and three anti-apoptotic decoys. This protein has generated tremendous excitement as a potential tumor-specific cancer therapeutic because, as a stable soluble trimer, it selectively induces apoptosis in many transformed cells but not in normal cells. Transcriptional activation of Apo2L/TRAIL by interferons (IFNs) through specific regulatory elements in its promoter, and possibly by a number of other cytokines, reveals its possible involvement in the activation of natural killer cells, cytotoxic T lymphocytes, and dendritic cells. In this review, we focus on the apoptosis signaling pathways stimulated by Apo2L/TRAIL, summarize what is known to date about the physiological role of this ligand and the potential for its application to cancer therapy.
Apo2配体或肿瘤坏死因子(TNF)相关凋亡诱导配体(Apo2L/TRAIL)是TNF基因超家族的几个成员之一,它通过与死亡受体结合来诱导细胞凋亡。与任何其他细胞因子相比,Apo2L/TRAIL不同寻常,因为它与一个复杂的受体系统相互作用:两个促凋亡死亡受体和三个抗凋亡诱饵受体。这种蛋白质作为一种潜在的肿瘤特异性癌症治疗药物引起了极大的关注,因为作为一种稳定的可溶性三聚体,它能在许多转化细胞中选择性地诱导凋亡,而在正常细胞中则不会。干扰素(IFN)通过其启动子中的特定调控元件,可能还通过许多其他细胞因子对Apo2L/TRAIL进行转录激活,这揭示了它可能参与自然杀伤细胞、细胞毒性T淋巴细胞和树突状细胞的激活。在这篇综述中,我们重点关注Apo2L/TRAIL刺激的细胞凋亡信号通路,总结目前已知的该配体的生理作用及其在癌症治疗中的应用潜力。