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Series GSE32222 Query DataSets for GSE32222
Status Public on Jan 04, 2012
Title Differential oestrogen receptor binding is associated with clinical outcome in breast cancer
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Oestrogen receptor-a (ER) is the defining and driving transcrip- tion factor in the majority of breast cancers and its target genes dictate cell growth and endocrine response, yet genomic under- standing of ER function has been restricted to model systems1­3. Here we map genome-wide ER-binding events, by chromatin immunoprecipitation followed by high-throughput sequencing (ChIP-seq), in primary breast cancers from patients with different clinical outcomes and in distant ER-positive metastases. We find that drug-resistant cancers still recruit ER to the chromatin, but that ER binding is a dynamic process, with the acquisition of unique ER-binding regions in tumours from patients that are likely to relapse. The acquired ER regulatory regions associated with poor clinical outcome observed in primary tumours reveal gene signatures that predict clinical outcome in ER-positive disease exclusively. We find that the differential ER-binding programme observed in tumours from patients with poor outcome is not due to the selection of a rare subpopulation of cells, but is due to the FOXA1-mediated reprogramming of ER binding on a rapid
time- scale. The parallel redistribution of ER and FOXA1 cis-regulatory elements in drug-resistant cellular contexts is supported by histological co-expression of ER and FOXA1 in metastatic samples. By establishing transcription-factor mapping in primary tumour material, we show that there is plasticity in ER-binding capacity, with distinct combinations of cis-regulatory elements linked with the different clinical outcomes.
 
Overall design Oestrogen receptor alpha (ER) binding was mapped genome wide in 15 primary ER-positive breast tumours and 3 ER-positive distant metastases. As a control, ER binding was also mapped in 2 ER-negative breast tumours. For cell line experiments, ER was mapped, in at least duplicate, in three ER-positive cell lines that respond to tamoxifen treatment, and 2 ER-positive cell lines that are resistant to tamoxifen treatment. Both ER and FOXA1 binding was mapped in MCF-7 cells, in duplicate, before and after treatment with a cocktail of mitogens (i.e. IGF-1, TNF-alpha, EGF and IL-6).
 
Contributor(s) Ross-Innes C, Stark R, Menon S
Citation(s) 22217937
Submission date Sep 19, 2011
Last update date Feb 21, 2019
Contact name Suraj Menon
E-mail suraj.menon@cruk.cam.ac.uk
Organization name Cambridge Research Institute, Cancer Research UK
Street address Li Ka Shing Center, Robinson Way
City Cambridge
ZIP/Postal code CB2 0RE
Country United Kingdom
 
Platforms (1)
GPL10999 Illumina Genome Analyzer IIx (Homo sapiens)
Samples (62)
GSM798383 SLX-1201.250.s_4
GSM798384 SLX-1881.334.s_1
GSM798385 SLX-2626.438.s_4
Relations
BioProject PRJNA147213
SRA SRP032421

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
GSE32222_RAW.tar 35.3 Mb (http)(custom) TAR (of TXT)
Processed data provided as supplementary file
Raw data not provided for this record

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