Journal article
The potential for epigenetic analysis of paediatric CNS tumours to improve diagnosis, treatment and prognosis
A Sexton-Oates, D MacGregor, A Dodgshun, R Saffery
Annals of Oncology | ELSEVIER | Published : 2015
Abstract
Tumours of central nervous system (CNS) origin are the second most prevalent group of cancers in children, yet account for the majority of childhood cancer-related deaths. Such tumours show diverse location, cell type of origin, disease course and long-term outcome, both across and within tumour types, making treatment problematic and contributing to the relatively modest progress in reducing mortality over recent decades. As technological advances begin to reveal the genetic landscape of all cancers, it is becoming increasingly clear that genetic disruption represents only one 'layer' of molecular disruption associated with disease aetiology. Obtaining a full understanding of tumour behavio..
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Funding Acknowledgements
This work was supported by the National Health and Medical Research Council and the Cancer in Kids Auxillary at the Royal Children's Hospital, Melbourne, Australia (no grant numbers apply). AS-O is supported by an Australian Postgraduate Award and the Murdoch Childrens Research Institute. RS is supported by the National Health and Medical Research Institute, Australia.