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dc.contributor.authorCavazzana, Andrea
dc.contributor.authorDi Cristofano, Claudio
dc.contributor.authorPerri, Patrizia
dc.contributor.authorGambini, Claudio
dc.contributor.authorLongo, Luca
dc.contributor.authorMazzocco, Katia
dc.contributor.authorMoretti, Stefano
dc.contributor.authorBonassi, Stefano
dc.contributor.authorTonini, Gian Paolo
dc.contributor.authorCoco, Simona
dc.contributor.authorDefferrari, Raffaella
dc.contributor.authorScaruffi, Paola
dc.date.accessioned2010-10-18T10:15:27Z
dc.date.available2010-10-18T10:15:27Z
dc.date.issued2005
dc.identifier.urihttps://basepub.dauphine.fr/handle/123456789/4942
dc.language.isoenen
dc.subjectneuroblastic cellen
dc.subjectSchwann cellen
dc.subjectlaser capture microdissectionen
dc.subjectgene expression profilingen
dc.subjectcomparative genomic hybridisationen
dc.subjectloss of heterozygosityen
dc.subjectneuroblastomaen
dc.subject.ddc515en
dc.titleGenome analysis and gene expression profiling of neuroblastoma and ganglioneuroblastoma reveal differences between neuroblastic and Schwannian stromal cellsen
dc.typeArticle accepté pour publication ou publié
dc.contributor.editoruniversityotherLaboratory of Italian Neuroblastoma Foundation, Advanced Biotechnology Center (ABC);Italie
dc.contributor.editoruniversityotherSection of Molecular Pathology, Division of Oncology, Pisa University Hospital, Via Roma;Italie
dc.contributor.editoruniversityotherUnit of Translational Paediatric Oncology, National Institute for Cancer Research (IST);Italie
dc.contributor.editoruniversityotherDepartment of Pathology, Gaslini Children's Hospital;Italie
dc.contributor.editoruniversityotherUnit of Molecular Epidemiology, National Institute for Cancer Research (IST;Italie
dc.description.abstractenNeuroblastic tumours are a group of paediatric cancers with marked morphological heterogeneity. Neuroblastoma (Schwannian stroma-poor) (NB-SP) is composed of undifferentiated neuroblasts. Ganglioneuroblastoma intermixed (Schwannian stroma-rich) (GNBi-SR) is predominantly composed of Schwannian stromal (SS) and neuroblastic (Nb) cells. There are contrasting reports suggesting that SS cells are non-neoplastic. In the present study, laser capture microdissection (LCM) was employed to isolate SS and Nb cells. Chromosome 1p36 deletion and MYCN gene amplification were found to be associated in two out of seven NB-SPs, whereas no abnormalities were observed in five GNBi-SRs. In some cases, loss of heterozygosity (LOH) at 1p36 loci was detected in Nb cells but not in the bulk tumour by LCM; furthermore, LOH was also identified in both SS and tumour tissue of a GNBi-SR. DNA gain and loss studied by comparative genomic hybridization were observed at several chromosome regions in NB-SP but in few regions of GNBi-SR. Finally, gene expression profiles studied using an oligo-microarray technique displayed two distinct signatures: in the first, 32 genes were expressed in NB-SP and in the second, 14 genes were expressed in GNBi-SR. The results show that NB-SP is composed of different morphologically indistinguishable malignant cell clones harbouring cryptic mutations that are detectable only after LCM. The degree of DNA imbalance is higher in NB-SP than in GNBi-SR. However, when the analysis of chromosome 1p36 is performed at the level of microdissection, LOH is also observed in SS cells. These data provide supportive evidence that SS cells have a less aggressive phenotype and play a role in tumour maturation. Copyright © 2005 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.en
dc.relation.isversionofjnlnameJournal of Pathology
dc.relation.isversionofjnlvol207en
dc.relation.isversionofjnlissue3en
dc.relation.isversionofjnldate2005-11
dc.relation.isversionofjnlpages346-357en
dc.relation.isversionofdoihttp://dx.doi.org/10.1002/path.1843en
dc.description.sponsorshipprivateouien
dc.relation.isversionofjnlpublisherWileyen
dc.subject.ddclabelanalyseen


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