Pediatric Ependymoma: Biological Perspectives

Kilday, J.-P.; Rahman, R.; Dyer, S.; Ridley, L.; Lowe, J.; Coyle, B.; Grundy, R.

Abstract

Pediatric ependymomas are enigmatic tumors that continue to present a clinical management challenge despite advances in neurosurgery, neuroimaging techniques, and radiation therapy. Difficulty in predicting tumor behavior from clinical and histological factors has shifted the focus to the molecular and cellular biology of ependymoma in order to identify new correlates of disease outcome and novel therapeutic targets. This article reviews our current understanding of pediatric ependymoma biology and includes a meta-analysis of all comparative genomic hybridization (CGH) studies done on primary ependymomas to date, examining more than 300 tumors. From this meta-analysis and a review of the literature, we show that ependymomas in children exhibit a different genomic profile to those in adults and reinforce the evidence that ependymomas from different locations within the central nervous system (CNS) are distinguishable at a genomic level. Potential biological markers of prognosis in pediatric ependymoma are assessed and the ependymoma cancer stem cell hypothesis is highlighted with respect to tumor resistance and recurrence. We also discuss the shifting paradigm for treatment modalities in ependymoma that target molecular alterations in tumor-initiating cell populations. (Mol Cancer Res 2009;7(6):765–86)

Citation

Kilday, J.-P., Rahman, R., Dyer, S., Ridley, L., Lowe, J., Coyle, B., & Grundy, R. (2009). Pediatric Ependymoma: Biological Perspectives. Molecular Cancer Research, 7(6), 765-786. https://doi.org/10.1158/1541-7786.mcr-08-0584

• Journal Article Type: Article
• Acceptance Date: Mar 19, 2009
• Online Publication Date: Jun 16, 2009
• Publication Date: Jun 1, 2009
• Deposit Date: Dec 5, 2018
• Journal: Molecular Cancer Research
• Print ISSN: 1541-7786
• Electronic ISSN: 1557-3125
• Publisher: American Association for Cancer Research
• Peer Reviewed: Peer Reviewed
• Volume: 7
• Issue: 6
• Pages: 765-786
• DOI: https://doi.org/10.1158/1541-7786.mcr-08-0584
• Public URL: https://nottingham-repository.worktribe.com/output/1370711
• Publisher URL: https://mcr.aacrjournals.org/content/7/6/765