Comparison of medulloblastoma and normal neural transcriptomes identifies a restricted set of activated genes
Comparison of medulloblastoma and normal neural transcriptomes identifies a restricted set of activated genes"
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ABSTRACT Over 1.4 million transcript tags expressed in 20 different human medulloblastomas were counted using serial analysis of gene expression. Digital gene expression profiles in the
medulloblastoma were compared to multiple regions of the normal human brain, revealing 30 transcripts with high expression in multiple tumors and little or no expression in the normal
cerebellum and other adult and pediatric brain regions. Using independent medulloblastoma samples and normal tissue, real-time PCR verified eight of nine selected genes as candidate
tumor-associated antigens. Differential protein expression for CD24, prolactin and Topo2A was further confirmed by immunohistochemical analysis using medulloblastoma and normal brain
sections and a tissue microarray. The genes highly expressed in the medulloblastoma include PRAME, a cancer-testis antigen and potential targets for immunotherapy. Access through your
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_Science_, 270, 484–487. Download references ACKNOWLEDGEMENTS Medulloblastoma samples were provided by the Duke Brain Tumor Bank and the Pediatric Oncology Group via the NIH Collaborative
Human Tissue Network. We thank Jennifer Shoemaker for statistics consulting, Dr Roger McLendon (Duke University Medical Center) for expert histopathology, Drs Anita Lal, Robert Beaty, Brian
Fee, Keith Killian and Janete Cerutti for providing SAGE data on normal tissues, Dennis W Rickman for expert immunohistochemistry assistance, and Dr Steven Jones, Jacquie Schein and members
of the BCGSC sequencing team for expert technical assistance. Funding was provided by the Cancer Genome Anatomy Project (NCI contract S98-146), NCI Grant U01 CA88128 and the Pediatric Brain
Tumor Foundation of the United States. AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Department of Pathology, Duke University Medical Center, Box 3156, Durham, 27710, NC, USA Kathy Boon,
Jennifer B Edwards, I-Mei Siu, Deric Olschner & Gregory J Riggins * Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, 21205, MD, USA Charles G Eberhart *
Sequencing Center, BC Cancer Agency, Vancouver, Canada Marco A Marra * Office of Cancer Genomics, National Cancer Institute, Bethesda, 20892, MD, USA Robert L Strausberg Authors * Kathy Boon
View author publications You can also search for this author inPubMed Google Scholar * Jennifer B Edwards View author publications You can also search for this author inPubMed Google
Scholar * I-Mei Siu View author publications You can also search for this author inPubMed Google Scholar * Deric Olschner View author publications You can also search for this author
inPubMed Google Scholar * Charles G Eberhart View author publications You can also search for this author inPubMed Google Scholar * Marco A Marra View author publications You can also search
for this author inPubMed Google Scholar * Robert L Strausberg View author publications You can also search for this author inPubMed Google Scholar * Gregory J Riggins View author
publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to Gregory J Riggins. RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS
ARTICLE CITE THIS ARTICLE Boon, K., Edwards, J., Siu, IM. _et al._ Comparison of medulloblastoma and normal neural transcriptomes identifies a restricted set of activated genes. _Oncogene_
22, 7687–7694 (2003). https://doi.org/10.1038/sj.onc.1207043 Download citation * Received: 24 June 2003 * Revised: 25 July 2003 * Accepted: 25 July 2003 * Published: 23 October 2003 * Issue
Date: 23 October 2003 * DOI: https://doi.org/10.1038/sj.onc.1207043 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a
shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative KEYWORDS * medulloblastoma *
tumor-associated antigens * SAGE * bioinformatics
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