Cancer Center, Medical Research Institute, Southwest University, Chongqing 400716, China.
Department of Neurosurgery, Children's Hospital of Chongqing Medical University, Chongqing 400014, China.
Biomolecules. 2021 Apr 14;11(4):572. doi: 10.3390/biom11040572.
The tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) shows a promising therapeutic potential in cancer treatment as it exclusively causes apoptosis in a broad spectrum of cancer cells through triggering the extrinsic apoptosis pathway via binding to cognate death receptors, with negligible toxicity in normal cells. However, most cancers, including glioblastoma multiforme (GBM), display TRAIL resistance, hindering its application in clinical practice. Recent studies have unraveled novel mechanisms in regulating TRAIL-induced apoptosis in GBM and sought effective combinatorial modalities to sensitize GBM to TRAIL treatment, establishing pre-clinical foundations and the reasonable expectation that the TRAIL/TRAIL death receptor axis could be harnessed to treat GBM. In this review, we will revisit the status quo of the mechanisms of TRAIL resistance and emerging strategies for sensitizing GBM to TRAIL-induced apoptosis and also discuss opportunities of TRAIL-based combinatorial therapies in future clinical use for GBM treatment.
肿瘤坏死因子(TNF)相关凋亡诱导配体(TRAIL)在癌症治疗中具有广阔的应用前景,因为它通过与同源死亡受体结合,通过触发外在凋亡途径,在广泛的癌细胞中特异性诱导凋亡,而对正常细胞几乎没有毒性。然而,大多数癌症,包括多形性胶质母细胞瘤(GBM),表现出对 TRAIL 的耐药性,阻碍了其在临床实践中的应用。最近的研究揭示了调节 GBM 中 TRAIL 诱导凋亡的新机制,并寻求有效的联合方式使 GBM 对 TRAIL 治疗敏感,为临床前基础和合理预期奠定了基础,即 TRAIL/TRAIL 死亡受体轴可用于治疗 GBM。在这篇综述中,我们将重新审视 TRAIL 耐药性的机制现状和使 GBM 对 TRAIL 诱导凋亡敏感的新策略,并讨论基于 TRAIL 的联合治疗在未来 GBM 治疗中的临床应用机会。