Department of Molecular & Human Genetics, Cancer Genetics Laboratory, Institute of Science, Banaras Hindu University, Varanasi, 221005, India.
Department of Surgical Oncology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, 221005, India.
Future Oncol. 2021 Feb;17(5):581-596. doi: 10.2217/fon-2020-0727. Epub 2021 Jan 6.
TNF-related apoptosis-inducing ligand (TRAIL), a member of the TNF superfamily, can induce apoptosis in cancer cells, sparing normal cells when bound to its associated death receptors (DR4/DR5). This unique mechanism makes TRAIL a potential anticancer therapeutic agent. However, clinical trials of recombinant TRAIL protein and TRAIL receptor agonist monoclonal antibodies have shown disappointing results due to its short half-life, poor pharmacokinetics and the resistance of the cancer cells. This review summarizes TRAIL-induced apoptotic and survival pathways as well as mechanisms leading to apoptotic resistance. Recent development of methods to overcome cancer cell resistance to TRAIL-induced apoptosis, such as protein modification, combination therapy and TRAIL-based gene therapy, appear promising. We also discuss the challenges and opportunities in the development of TRAIL-based therapies for the treatment of human cancers.
肿瘤坏死因子相关凋亡诱导配体(TRAIL)是肿瘤坏死因子超家族的一员,与相关死亡受体(DR4/DR5)结合后能够诱导癌细胞凋亡,而对正常细胞则无影响。这种独特的机制使 TRAIL 成为一种有潜力的抗癌治疗药物。然而,由于其半衰期短、药代动力学差以及癌细胞的耐药性,重组 TRAIL 蛋白和 TRAIL 受体激动型单克隆抗体的临床试验结果令人失望。本综述总结了 TRAIL 诱导的凋亡和存活途径以及导致凋亡耐药的机制。最近开发的克服癌细胞对 TRAIL 诱导凋亡耐药的方法,如蛋白质修饰、联合治疗和 TRAIL 基因治疗等,似乎很有前途。我们还讨论了基于 TRAIL 的癌症治疗方法的发展所面临的挑战和机遇。