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Series GSE27671 Query DataSets for GSE27671
Status Public on Jul 01, 2011
Title Genomic Aberrations in Paediatric Gliomas and Embryonal Tumours
Organism Homo sapiens
Experiment type Genome variation profiling by genome tiling array
Summary The pathogenesis of paediatric central nervous system tumours is still poorly understood. In an attempt to increase the knowledge of the genetic mechanisms underlying these tumours, we performed genome-wide screening of 17 paediatric gliomas and embryonal tumours using a combination of G-band karyotyping and array comparative genomic hybridisation (aCGH). G-banding revealed abnormal karyotypes in 56% of tumour samples (9 of 16; one failed in culture), whereas aCGH analysis found copy number aberrations in all 13 tumours that could be examined. Pilocytic astrocytomas (n=3) showed normal karyotypes or simple non-recurrent translocations by karyotyping, but revealed the now well-established recurrent gain of 7q34 by aCGH. Our series included one anaplastic oligoastrocytoma, tumours that have not previously been characterised genomically in children, and an anaplastic neuroepithelial tumour (probably an oligoastrocytoma); both tumours showed losses of chromosomes 14 by G-banding as well as structural aberrations of the long arm of chromosome 6, and loss of 14q, 17p, and 22q by aCGH. Three supratentorial primitive neuroectodermal tumours (n=5) showed aberrant karyotypes; two near-diploid with mainly structural changes and one near-triploid with several trisomies including gains of one copy of chromosomes 1, 2, and 7. aCGH confirmed these findings and revealed additional recurrent gains of 1q21-44, 3p21, and 3q29. We also describe cytogenetically for the first time a cribriform neuroepithelial tumour, a recently identified variant of atypical teratoid/rhabdoid tumour with a favourable prognosis, which showed loss of 1p33, 4q13.2, 10p12.31, 10q11.22, and 22q by aCGH.
 
Overall design Tumour sample analysed with control DNA (supplied by Agilent)
 
Contributor(s) Dahlback HS, Brandal P, Gorunova L, Meling TR, Krossnes BK, Heim S
Citation(s) 21717527
Submission date Mar 03, 2011
Last update date Dec 06, 2012
Contact name Hanne-Sofie S Dahlback
E-mail(s) h.s.s.dahlback@medisin.uio.no
Organization name The Norwegian Radium Hospital
Department Section for Cancer Cytogenetics
Street address Montebello
City Oslo
ZIP/Postal code 0310
Country Norway
 
Platforms (1)
GPL10123 Agilent-022060 SurePrint G3 Human CGH Microarray 4x180K (Feature Number version)
Samples (13)
GSM685387 Pilocytic astrocytoma 05-0129
GSM685388 Pilocytic astrocytoma 05-0270
GSM685389 Glioblastoma 07-0705
Relations
BioProject PRJNA138183

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE27671_RAW.tar 399.4 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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