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PMID: 18716556 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Frequent gains at chromosome 7q34 involving BRAF in pilocytic astrocytoma.

Journal of neuropathology and experimental neurology ·Vol. 67 ·No. 9 ·2008-09-00 ·Pages 878-87

Bar EE, Lin A, Tihan T, Burger PC, Eberhart CG

Abstract

Relatively little is known about the molecular changes that promote the formation or growth of pilocytic astrocytomas. We investigated genomic alterations in 25 pilocytic astrocytomas, including 5 supratentorial and 20 posterior fossa tumors, using oligonucleotide array comparative genomic hybridization. Large changes were identified in 7 tumors and included gains of chromosomes 5, 6, and 7 and losses of chromosomes 16, 17, 19, and 22. The most common alteration was a 1.9-MB region of low-level gain at chromosome 7q34 identified in 17 of 20 posterior fossa tumors. In most tumors, the region of gain ended within the BRAF locus and encompassed only exons that encode the BRAF kinase domain. We confirmed copy number increase at the 7q34 locus using quantitative polymerase chain reaction with primers adjacent to the HIPK2, RAB19B, and BRAF genes. Western blot analysis revealed that 3 of 6 pilocytic astrocytomas with 7q34 gain contained high levels of phosphorylated extracellular signal-related kinase (ERK) and nitrogen-activated protein kinase/ERK kinase (MEK), while 1 tumor lacking 7q34 gain and 2 normal brain specimens did not. Immunohistochemical stains of a tissue microarray containing 43 pilocytic astrocytoma identified ERK phosphorylation in 35 (81%). These data indicate that focal gains at chromosome 7q34 and increased BRAF-MEK-ERK signaling are common findings in sporadic pilocytic astrocytomas.

MeSH Terms
Adolescent Adult Astrocytoma/genetics Blotting, Western Brain Neoplasms/genetics Child Child, Preschool Chromosomes, Human, Pair 7/genetics Extracellular Signal-Regulated MAP Kinases/metabolism Female Gene Dosage Humans Immunohistochemistry MAP Kinase Kinase Kinases/metabolism Male Oligonucleotide Array Sequence Analysis Proto-Oncogene Proteins B-raf/genetics Reverse Transcriptase Polymerase Chain Reaction Signal Transduction/physiology Tissue Array Analysis
Chemicals
BRAF protein, human Proto-Oncogene Proteins B-raf Extracellular Signal-Regulated MAP Kinases MAP Kinase Kinase Kinases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Bar Eli E
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA. ebar1@jhmi.edu
Lin Alex
Tihan Tarik
Burger Peter C
Eberhart Charles G
Article Info
Journal
Journal of neuropathology and experimental neurology
Abbr.
J Neuropathol Exp Neurol
ISSN
0022-3069
Published
2008-09-00
Pages
878-87
Language
English
Region
England
NLM ID
2985192R
Subset
IM
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