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Series GSE152202 Query DataSets for GSE152202
Status Public on Jun 11, 2020
Title Reduced representation bisulfite sequencing (RRBS) of breast cancer cell lines
Organism Homo sapiens
Experiment type Methylation 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 To identify regulatory regions specific to basal-like breast cancer, reduced representation bisulfite sequencing (RRBS) was performed on 28 breast cancer cell lines (18 basal-like and 10 luminal) in order to measure DNA methylation across the genome.
 
Contributor(s) Varley K
Citation(s) 32816914, 35221336
Submission date Jun 10, 2020
Last update date Mar 30, 2022
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)
GPL10999 Illumina Genome Analyzer IIx (Homo sapiens)
Samples (28)
GSM4608956 2LMP_RRBS
GSM4608957 BT-20_RRBS
GSM4608958 BT-474_RRBS
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 PRJNA638632
SRA SRP266790

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SOFT formatted family file(s) SOFTHelp
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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE152202_BrCa_cell_lines_RRBS.txt.gz 10.1 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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