NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE98330 Query DataSets for GSE98330
Status Public on Feb 23, 2018
Title Changes in chromatin state reveal a central role for the transcription factor ARNT2, in the control of glioblastoma stem cell tumorigenicity
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Although a growing body of evidence indicates that the phenotypic plasticity exhibited by glioblastoma cells plays a central role in tumor development and post-therapy recurrence, the master drivers of their aggressiveness remain elusive. Here we mapped the changes in the transcriptionally permissive (H3K4me3) and repressive (H3K27me3) epigenetic histone marks accompanying the repression of glioblastoma stem cells (GSC) tumorigenicity. Genes with changing marks delineated a network of transcription factors related to cancerous behavior, stem state, and neural development, which highlighted a previously unsuspected association between repression of ARNT2 and loss of cell tumorigenicity. Immunohistochemistry confirmed ARNT2 expression in cell sub-populations of patients’ glioblastoma. Its transcriptional repression was consistently found in non-tumorigenic glioblastoma cells, compared to tumorigenic cells. Moreover, ARNT2 expression correlated with a stem signature at both the tissue level within the tumor core and at the single cell level in the patients’ tumors. ARNT2 knockdown decreased expression of the transcription factors SOX9, POU3F2 and OLIG2 known promoters of glioblastoma cell tumorigenicity, and repressed GSC tumorigenic properties in vivo. Our results unveil ARNT2 as a master gene of the glioblastoma tumorigenic cell signature, located at a node of the transcription factor network controlling glioblastoma cell aggressiveness.
 
Overall design Histone modification profiling for two different marks by ChIP-Seq in glioblastoma stem-like cells and glioblastoma stem-like cells transduced with miR-302-367
 
Contributor(s) Bogeas A, Parinello H, Rialle S, Defrance M, Lejeune F, Junier M, Chneiweiss H
Citation(s) 29149419
Submission date Apr 28, 2017
Last update date May 15, 2019
Contact name Alexandra Bogeas
E-mail(s) alexandra.bogeas@inserm.fr
Organization name Inserm U1130, CNRS UMR 8246,University P. & M. Curie
Street address 7 quai St Bernard
City Paris
ZIP/Postal code 75005
Country France
 
Platforms (1)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (6)
GSM2592330 TG1 H3K4me3
GSM2592331 TG1 H3K27me3
GSM2592332 TG1 Input (A)
Relations
BioProject PRJNA384724
SRA SRP105406

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
GSE98330_macs14_A_K27_vs_A_INP_p10e-5_nomodel_shiftsize110_peaks.bed.gz 342.2 Kb (ftp)(http) BED
GSE98330_macs14_A_K4_vs_A_INP_p10e-5_nomodel_shiftsize112_peaks.bed.gz 386.6 Kb (ftp)(http) BED
GSE98330_macs14_B_K27_vs_B_INP_p10e-5_nomodel_shiftsize100_peaks.bed.gz 265.0 Kb (ftp)(http) BED
GSE98330_macs14_B_K4_vs_B_INP_p10e-5_nomodel_shiftsize090_peaks.bed.gz 449.2 Kb (ftp)(http) BED
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap