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Series GSE152203 Query DataSets for GSE152203
Status Public on Jun 11, 2020
Title STAT3 and GR cooperate to drive basal-like triple negative breast cancer gene expression and proliferation
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Breast cancers can be divided into subtypes with different prognoses and treatment responses based on global gene expression differences. This study utilized integrated analysis of DNA methylation, chromatin accessibility, transcription factor binding, and gene expression in large collections of breast cancer cell lines and patient tumors to identify transcription factors responsible for the basal-like gene expression program. The results of this study indicate that glucocorticoid receptor (GR) and signal transducer and activator of transcription 3 (STAT3) bind to the same genomic regulatory regions that are specifically open and unmethylated in basal-like breast cancer. These transcription factors cooperate to regulate expression of hundreds of genes in the basal-like gene expression signature and these downstream genes are associated with poor prognosis in patients.
 
Overall design Transcription factor ChIP-seq for GR and STAT3 was performed in TNBC cell lines, SUM159, MDA-MB-231, HCC1937, HCC70, HCC1187, and luminal cell lines MDA-MB-361, BT-474, MDA-MB-453, and MCF-7. STAT3 and GR ChIP-seq was performed after 1hr vehicle control induction (ethanol) and 100nM Dexamethasone induction respectively.
 
Contributor(s) Varley K
Citation(s) 32816914
Submission date Jun 10, 2020
Last update date Nov 05, 2020
Contact name Katherine E Varley
E-mail(s) kt.varley@hci.utah.edu
Organization name Huntsman Cancer Institute University of Utah
Department Department of Oncological Sciences
Lab Varley Lab
Street address 2000 Circle of Hope, Room 3719
City Salt Lake City
State/province UT
ZIP/Postal code 84112
Country USA
 
Platforms (1)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (18)
GSM4608984 BT474_STAT3_ChIP-seq
GSM4608985 HCC1187_STAT3_ChIP-seq
GSM4608986 HCC1937_STAT3_ChIP-seq
This SubSeries is part of SuperSeries:
GSE152205 Integrated analysis of DNA methylation, chromatin accessibility, transcription factor binding, and gene expression in large collections of breast cancer cell lines and patient tumors
Relations
BioProject PRJNA638631
SRA SRP266791

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Supplementary file Size Download File type/resource
GSE152203_ForGEO_STAT3_GR_ChIP_SharedPeakCounts.txt.gz 2.9 Mb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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