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Patient-derived orthotopic xenografts of pediatric brain tumors: a St. Jude resource.

Authors :
Smith KS
Xu K
Mercer KS
Boop F
Klimo P
DeCupyere M
Grenet J
Robinson S
Dunphy P
Baker SJ
Ellison DW
Merchant TE
Upadayaya SA
Gajjar A
Wu G
Orr BA
Robinson GW
Northcott PA
Roussel MF
Source :
Acta neuropathologica [Acta Neuropathol] 2020 Aug; Vol. 140 (2), pp. 209-225. Date of Electronic Publication: 2020 Jun 10.
Publication Year :
2020

Abstract

Pediatric brain tumors are the leading cause of cancer-related death in children. Patient-derived orthotopic xenografts (PDOX) of childhood brain tumors have recently emerged as a biologically faithful vehicle for testing novel and more effective therapies. Herein, we provide the histopathological and molecular analysis of 37 novel PDOX models generated from pediatric brain tumor patients treated at St. Jude Children's Research Hospital. Using a combination of histopathology, whole-genome and whole-exome sequencing, RNA-sequencing, and DNA methylation arrays, we demonstrate the overall fidelity and inter-tumoral molecular heterogeneity of pediatric brain tumor PDOX models. These models represent frequent as well as rare childhood brain tumor entities, including medulloblastoma, ependymoma, atypical teratoid rhabdoid tumor, and embryonal tumor with multi-layer rosettes. PDOX models will be valuable platforms for evaluating novel therapies and conducting pre-clinical trials to accelerate progress in the treatment of brain tumors in children. All described PDOX models and associated datasets can be explored using an interactive web-based portal and will be made freely available to the research community upon request.

Details

Language :
English
ISSN :
1432-0533
Volume :
140
Issue :
2
Database :
MEDLINE
Journal :
Acta neuropathologica
Publication Type :
Academic Journal
Accession number :
32519082
Full Text :
https://doi.org/10.1007/s00401-020-02171-5