Overlay analysis of the oligonucleotide array gene expression profiles and copy number abnormalities as determined by array comparative genomic hybridization in medulloblastomas

Combined analysis of gene expression array data and array‐based comparative genomic hybridization data have been used in a series of 26 pediatric brain tumors to define up‐ and downregulated genes that coincide with losses, gains, and amplifications involving specific chromosome regions. Frequent lo...

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Bibliographic Details
Published inGenes chromosomes & cancer Vol. 46; no. 1; pp. 53 - 66
Main Authors Lo, Ken C., Rossi, Michael R., Burkhardt, Tania, Pomeroy, Scott L., Cowell, John K.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.01.2007
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Summary:Combined analysis of gene expression array data and array‐based comparative genomic hybridization data have been used in a series of 26 pediatric brain tumors to define up‐ and downregulated genes that coincide with losses, gains, and amplifications involving specific chromosome regions. Frequent losses were defined in chromosome arms 3q, 6q, 8p, 10q, 16q, 17p, and gains were identified in chromosome 7, and chromosome arms 9p and 17q. Amplification of a 2p region was seen in only one tumor, which corresponded to increased expression of the MYCN and DDX1 genes. To facilitate the analysis of the two data sets, we have developed a custom overlay tool that defines genes that are underexpressed in regions of deletions and overexpressed in regions of gain, across the genome and specifically within regions showing recurrent involvement in medulloblastomas. © 2006 Wiley‐Liss, Inc.
Bibliography:National Cancer Institute Roswell Park Cancer Center - No. CA 16056
ark:/67375/WNG-SS2SDVK5-K
NIH - No. CA104504; No. CA109467; No. CA105607
istex:AEB6C85DB0DAEDD3CA3A9D8878B3D6FBC1E5B6EC
ArticleID:GCC20388
Thrasher Research Foundation
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1045-2257
1098-2264
DOI:10.1002/gcc.20388