Department of Physiology & Medical Physics, Royal College of Surgeons in Ireland, 31A York Street, Dublin, D02 YN77, Ireland.
National Children's Research Centre at Children's Health Ireland at Crumlin, Dublin, D12 N512, Ireland.
Cell Death Dis. 2022 May 14;13(5):460. doi: 10.1038/s41419-022-04900-y.
New, more effective therapeutics are required for the treatment of paediatric cancers. Current treatment protocols of cytotoxic treatments including chemotherapy trigger cancer-cell death by engaging the apoptosis pathway, and chemotherapy efficacy is frequently impeded by apoptosis dysregulation. Apoptosis dysregulation, through genetic or epigenetic mechanisms, is a feature of many cancer types, and contributes to reduced treatment response, disease progression and ultimately treatment resistance. Novel approaches are required to overcome dysregulated apoptosis signalling, increase the efficacy of cancer treatment and improve patient outcomes. Here, we provide an insight into current knowledge of how the apoptosis pathway is dysregulated in paediatric nervous system tumours, with a focus on TRAIL receptors, the BCL-2 proteins and the IAP family, and highlight preclinical evidence demonstrating that pharmacological manipulation of the apoptosis pathway can restore apoptosis signalling and sensitise cancer cells to treatment. Finally, we discuss the potential clinical implications of these findings.
需要新的、更有效的治疗方法来治疗儿科癌症。目前的细胞毒性治疗方案,包括化疗,通过激活细胞凋亡途径来诱导癌细胞死亡,而化疗的疗效经常受到细胞凋亡失调的阻碍。凋亡失调是许多癌症类型的一个特征,通过遗传或表观遗传机制,导致治疗反应降低、疾病进展,并最终导致治疗耐药。需要新的方法来克服失调的细胞凋亡信号,提高癌症治疗的疗效,并改善患者的预后。在这里,我们深入了解了细胞凋亡途径在小儿神经系统肿瘤中失调的机制,重点介绍了 TRAIL 受体、BCL-2 蛋白和 IAP 家族,并强调了临床前证据表明,对细胞凋亡途径的药理学干预可以恢复细胞凋亡信号,使癌细胞对治疗敏感。最后,我们讨论了这些发现的潜在临床意义。