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Brain Pathol. 2011 Jan;21(1):96-104. doi: 10.1111/j.1750-3639.2010.00455.x.

Molecular diagnostics in embryonal brain tumors.

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  • 1Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Md 21205, USA. ceberha@jhmi.edu

Abstract

Embryonal brain tumors are a heterogeneous group of neoplasms united by the presence of poorly differentiated stem-like cells. Molecular details are increasingly being used to separate them into biologically and clinically meaningful groups. For medulloblastoma, integrated mRNA expression profiling and DNA analysis by a number of research groups defines 4-6 distinctive molecular variants. A subset with prominent Wnt activity is associated with good clinical outcomes and classic histology. Medulloblastomas showing a Hedgehog gene expression signature are frequently of the desmoplastic/nodular subtype. Interestingly, Hedgehog activity is found in tumors arising either in infants or older teenagers and adults. The association of clinically aggressive medulloblastoma with MYC expression, large cell/anaplastic change and high levels of photoreceptor differentiation transcripts has also been noted in several studies. Immunohistochemical analysis of just one or two genes per molecular medulloblastoma variant may be sufficient for accurate classification, and this would be of great practical utility if validated. Advances have also been made in the classification of central nervous system (CNS) Primitive Neuroectodermal Tumors (PNET), as several groups have identified an amplicon at chromosome 19q13.41-42, which appears to define a unique PNET subtype associated with prominent true rosettes, young age and very poor outcomes.

© 2010 The Author; Brain Pathology © 2010 International Society of Neuropathology.

PMID:
21129063
[PubMed - indexed for MEDLINE]
PMCID:
PMC3575597
Free PMC Article
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