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Status |
Public on Oct 16, 2012 |
Title |
Gene expression data from glioblastoma tumor samples |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
Glioblastoma (GBM) is an incurable brain tumor carrying a dismal prognosis, which displays considerable heterogeneity. We have recently identified recurrent H3F3A mutations affecting two critical positions of histone H3.3 (K27, G34) in one-third of pediatric GBM. Here we show that each of these H3F3A mutations defines an epigenetic subgroup of GBM with a distinct global methylation pattern, and are mutually exclusive with IDH1 mutation (characterizing a CpG-Island Methylator Phenotype (CIMP) subgroup). Three further epigenetic subgroups were enriched for hallmark genetic events of adult GBM (EGFR amplification, CDKN2A/B deletion) and/or known transcriptomic signatures. We also demonstrate that the two H3F3A mutations give rise to GBMs in separate anatomic compartments, with differential regulation of OLIG1/2 and FOXG1, possibly reflecting different cellular origins. To further dissect the biological differences between epigenetic glioblastoma subgroups, we looked at the transcriptomic profiles of glioblastoma samples.
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Overall design |
46 glioblastoma samples from patients of various ages were selected for RNA extraction and hybridization on Affymetrix Affymetrix Human Genome U133 Plus 2.0 Arrays.
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Contributor(s) |
Sturm D, Witt H, Hovestadt V, Khuong Quang D, Plass C, Jabado N, Pfister SM |
Citation(s) |
23079654 |
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Submission date |
Mar 02, 2012 |
Last update date |
Mar 25, 2019 |
Contact name |
Marcel Kool |
E-mail(s) |
[email protected]
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Phone |
00496221424636
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Organization name |
German Cancer Research Center
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Department |
Pediatric Neuro Oncology
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Street address |
Im Neuenheimer Feld 580
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City |
Heidelberg |
ZIP/Postal code |
69120 |
Country |
Germany |
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Platforms (1) |
GPL570 |
[HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array |
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Samples (46)
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Relations |
BioProject |
PRJNA153165 |