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Series GSE237769 Query DataSets for GSE237769
Status Public on Jul 24, 2023
Title Epigenetic therapy targets the 3D epigenome in endocrine-resistant breast cancer [CUT&RUN]
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Here we investigate the impact of epigenetic therapy with Decitabine in endocrine-resistant ER+ breast cancer by using patient-derived xenograft (PDX) models. Decitabine treatment restrained tumour growth, inhibited cell proliferation and resulted in significant loss of DNA methylation, particularly at enhancers and repetitive elements. Systematic integration of matched in situ Hi-C / PCHi-C, EPIC, RNA-seq and ChIP–seq datasets revealed widespread differences in epigenome regulation and enhancer-promoter communication with Decitabine. We find that loss of DNA methylation with Decitabine strongly affects the open (A) and closed (B) compartment structure and TAD boundary insulation. Our study identified and focused on key DNA methylation-dependent, enhancer ER binding sites that are activated in Decitabine-treated PDX tumours, enabling direct interactions between promoters and multiple distal enhancers, inducing expression of ER target genes and pathways. Overall, we demonstrate that epigenetic therapy inhibits tumour progression through to rewiring of ER-mediated 3D chromatin interactions and transcriptome programs. Our findings suggest that targeting the 3D epigenome with epigenetic therapies represents a promising strategy for anti-cancer treatment in ER+ endocrine resistant breast cancer patients.
 
Overall design To understand the Decitabine-induced molecular changes driving tumour regression on a global scale, we used in situ Hi-C to generate genome-wide 3D genome maps of PDX breast tumours treated with Decitabine. At the same time, we examined the genome-wide DNA methylation (EPIC Microarrays), promoter-anchored interactome (Promoter Capture Hi-C (PCHi-C)), transcription factor binding (ER and FOXA1 ChIP-seq) and gene expression (RNA-seq) in the same tumours.
 
Contributor(s) Achinger-Kawecka J
Citation(s) 38448820
Submission date Jul 19, 2023
Last update date Mar 13, 2024
Contact name Joanna Achinger-Kawecka
E-mail(s) [email protected]
Organization name South Australian Immunogenomics Cancer Institute
Street address AHMS Building, North Terrace
City Adelaide
State/province SA
ZIP/Postal code 5005
Country Australia
 
Platforms (1)
GPL18573 Illumina NextSeq 500 (Homo sapiens)
Samples (13)
GSM7648680 Gar15-13 Vehicle 1 CTCF
GSM7648681 Gar15-13 Vehicle 2 CTCF
GSM7648682 Gar15-13 Vehicle 3 CTCF
This SubSeries is part of SuperSeries:
GSE171074 The potential of epigenetic therapy to target the 3D epigenome in endocrine-resistant breast cancer
Relations
BioProject PRJNA996581

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
GSE237769_RAW.tar 8.5 Mb (http)(custom) TAR (of BED)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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