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Published in: Child's Nervous System 4/2012

01-04-2012 | Review Paper

Matching mice to malignancy: molecular subgroups and models of medulloblastoma

Authors: Jasmine Lau, Christin Schmidt, Shirley L. Markant, Michael D. Taylor, Robert J. Wechsler-Reya, William A. Weiss

Published in: Child's Nervous System | Issue 4/2012

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Abstract

Introduction

Medulloblastoma, the largest group of embryonal brain tumors, has historically been classified into five variants based on histopathology. More recently, epigenetic and transcriptional analyses of primary tumors have subclassified medulloblastoma into four to six subgroups, most of which are incongruous with histopathological classification.

Discussion

Improved stratification is required for prognosis and development of targeted treatment strategies, to maximize cure and minimize adverse effects. Several mouse models of medulloblastoma have contributed both to an improved understanding of progression and to developmental therapeutics. In this review, we summarize the classification of human medulloblastoma subtypes based on histopathology and molecular features. We describe existing genetically engineered mouse models, compare these to human disease, and discuss the utility of mouse models for developmental therapeutics. Just as accurate knowledge of the correct molecular subtype of medulloblastoma is critical to the development of targeted therapy in patients, we propose that accurate modeling of each subtype of medulloblastoma in mice will be necessary for preclinical evaluation and optimization of those targeted therapies.
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Metadata
Title
Matching mice to malignancy: molecular subgroups and models of medulloblastoma
Authors
Jasmine Lau
Christin Schmidt
Shirley L. Markant
Michael D. Taylor
Robert J. Wechsler-Reya
William A. Weiss
Publication date
01-04-2012
Publisher
Springer-Verlag
Published in
Child's Nervous System / Issue 4/2012
Print ISSN: 0256-7040
Electronic ISSN: 1433-0350
DOI
https://doi.org/10.1007/s00381-012-1704-1

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