Home > Institute Collections > W500 > Ewing Sarcoma PDX Models |
Contribution to a book | DKFZ-2024-02250 |
; ; ; ; ;
2021
Springer US
New York, NY
ISBN: 978-1-0716-1019-0 (print), 978-1-0716-1020-6 (electronic)
Please use a persistent id in citations: doi:10.1007/978-1-0716-1020-6_18
Abstract: Ewing sarcoma (EWS) is a rare malignant pediatric tumor and patient derived xenografts (PDXs) could represent a possibility to increase the number of available models to study this disease. Compared to cell derived xenografts (CDX), PDXs are reported to better recapitulate tumor microenvironment, heterogeneity, genetic and epigenetic features and are considered reliable models for their better predictive value when comparing preclinical efficacy and treatment response in patients. In this chapter, we extensively describe a method for generating Ewing sarcoma PDX models, for their validation and molecular characterization.
![]() |
The record appears in these collections: |