Targeting the apoptosis pathway to treat tumours of the paediatric nervous system

被引:18
作者
Fitzgerald, Marie-Claire [1 ,2 ]
O'Halloran, Philip J. [2 ,3 ]
Connolly, Niamh M. C. [1 ,4 ]
Murphy, Brona M. [1 ,2 ,4 ]
机构
[1] Royal Coll Surgeons Ireland, Dept Physiol & Med Phys, 31A York St, Dublin D02 YN77, Ireland
[2] Childrens Hlth Ireland Crumlin, Natl Childrens Res Ctr, Dublin D12 N512, Ireland
[3] Queen Elizabeth Hosp, Dept Neurosurg, Birmingham, W Midlands, England
[4] Royal Coll Surgeons Ireland, Ctr Syst Med, 31A York St, Dublin D02 YN77, Ireland
关键词
TRAIL-INDUCED APOPTOSIS; BCL-X-L; SENSITIVE RESPONSE ELEMENT; MCL-1; DOWN-REGULATION; NEUROBLASTOMA-CELLS; INTERFERON-GAMMA; CYTOCHROME-C; INTRACRANIAL EPENDYMOMAS; DIFFERENTIAL EXPRESSION; SURVIVIN EXPRESSION;
D O I
10.1038/s41419-022-04900-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
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页数:10
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