Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/67545

TítuloA distinct spectrum of copy number aberrations in pediatric high-grade gliomas
Autor(es)Bax, Dorine A.
Mackay, Alan
Little, Suzanne E.
Carvalho, Diana
Pereira, Marta Sofia Carvalho Ribeiro Viana
Tamber, Narinder
Grigoriadis, Anita E.
Ashworth, Alan
Reis, R. M.
Ellison, David W.
Al-Sarraj, Safa
Hargrave, Darren
Jones, Chris
Palavras-chaveAdolescent
Adult
Brain Neoplasms
Child
Child, Preschool
Comparative Genomic Hybridization
Gene Amplification
Gene Deletion
Glioblastoma
Glioma
Humans
DNA Copy Number Variations
DataJul-2010
EditoraAmerican Association for Cancer Research
RevistaClinical Cancer Research
CitaçãoBax, D. A., Mackay, A., Little, S. E., Carvalho, D., et. al. (2010). A distinct spectrum of copy number aberrations in pediatric high-grade gliomas. Clinical cancer research, 16(13), 3368-3377
Resumo(s)As genome-scale technologies begin to unravel the complexity of the equivalent tumors in adults, we can attempt detailed characterization of high-grade gliomas in children, that have until recently been lacking. Toward this end, we sought to validate and extend investigations of the differences between pediatric and adult tumors. Purpose: As genome-scale technologies begin to unravel the complexity of the equivalent tumors in adults, we can attempt detailed characterization of high-grade gliomas in children, that have until recently been lacking. Toward this end, we sought to validate and extend investigations of the differences between pediatric and adult tumors. Experimental Design: We carried out copy number profiling by array comparative genomic hybridization using a 32K bacterial artificial chromosome platform on 63 formalin-fixed paraffin-embedded cases of high-grade glioma arising in children and young people (<23 years). Results: The genomic profiles of these tumors could be subclassified into four categories: those with stable genomes, which were associated with a better prognosis; those with aneuploid and those with highly rearranged genomes; and those with an amplifier genotype, which had a significantly worse clinical outcome. Independent of this was a clear segregation of cases with 1q gain (more common in children) from those with concurrent 7 gain/10q loss (a defining feature of adults). Detailed mapping of all the amplification and deletion events revealed numerous low-frequency amplifications, including IGF1R, PDGFRB, PIK3CA, CDK6, CCND1, and CCNE1, and novel homozygous deletions encompassing unknown genes, including those at 5q35, 10q25, and 22q13. Despite this, aberrations targeting the “core signaling pathways” in adult glioblastomas are significantly underrepresented in the pediatric setting. Conclusions: These data highlight that although there are overlaps in the genomic events driving gliomagenesis of all ages, the pediatric disease harbors a distinct spectrum of copy number aberrations compared with adults.
TipoArtigo
URIhttps://hdl.handle.net/1822/67545
DOI10.1158/1078-0432.CCR-10-0438
ISSN1078-0432
e-ISSN1557-3265
Versão da editorahttps://clincancerres.aacrjournals.org/content/16/13/3368.short
Arbitragem científicayes
AcessoAcesso aberto
Aparece nas coleções:ICVS - Artigos em revistas internacionais / Papers in international journals

Ficheiros deste registo:
Ficheiro Descrição TamanhoFormato 
Bax-2010-A-distinct-spectrum-of-copy-number-.pdf602,58 kBAdobe PDFVer/Abrir

Partilhe no FacebookPartilhe no TwitterPartilhe no DeliciousPartilhe no LinkedInPartilhe no DiggAdicionar ao Google BookmarksPartilhe no MySpacePartilhe no Orkut
Exporte no formato BibTex mendeley Exporte no formato Endnote Adicione ao seu ORCID