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Series GSE95386 Query DataSets for GSE95386
Status Public on Feb 23, 2018
Title TRIM24 is an oncogenic transcriptional co-activator of STAT3 in glioblastoma
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Aberrant amplication and mutations of epidermal growth factor receptor (EGFR) are the most common oncogenic events in glioblastoma (GBM), but the mechanisms by which they promote aggressive pathogenesis are not well understood. Here, we determined that non-canonical histone signature acetylated H3 lysine 23 (H3K23ac)-binding protein tripartite motif-containing 24 (TRIM24) is upregulated in clinical specimens of glioblastoma and is required for EGFR-driven tumorigenesis.
 
Overall design Examination of effects of TRIM24 knockdown or EGFRvIII on differential gene expression in glioma cells.
 
Contributor(s) Feng H
Citation(s) 29129908
Submission date Feb 27, 2017
Last update date May 15, 2019
Contact name Haizhong Feng
E-mail(s) fenghaizhong@sjtu.edu.cn
Phone 862168383921
Organization name Shanghai Jiao Tong University
Department Ren Ji Hospital
Street address Pujian Road 160
City Shanghai
State/province Shanghai
ZIP/Postal code 200127
Country China
 
Platforms (1)
GPL20795 HiSeq X Ten (Homo sapiens)
Samples (8)
GSM2509626 LN229/shControl (WGC090194)
GSM2509627 LN229/EGFRvIII/shControl (WGC090195)
GSM2509628 LN229/EGFRvIII/shTRIM24-1# (WGC090200)
Relations
BioProject PRJNA376867
SRA SRP100743

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
GSE95386_RAW.tar 9.4 Mb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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