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Status |
Public on Aug 09, 2018 |
Title |
Bivalent chromatin domains in ovarian tumours at initial presentation identify genes predisposed to DNA hypermethylation during acquired resistance to chemotherapy [gene expression] |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
We have used ChIP-seq to characterize genome-wide positioning of H3K4me3 and H3K27me3 associated chromatin in primary high-grade serous ovarian carcinoma and normal ovarian surface and fallopian tube tissue. Sets of genes with proximal bivalent marks were defined using this data and subsequently evaluated as signatures of systematic change in DNA methylation and gene expression between pairs of tissue samples taken from patients at primary presentation and relapse following chemotherapy. Gene expression microarrays from primary tumours were used to assess transcriptional associations of chromatin marks identified in tumours through ChIP-seq
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Overall design |
RNA was extracted from four primary tumours and hybridized to Affymetrix microarrays. For each tumour, distribution of mas5 detection calls was compared for gene sets with H3K4me3 or H3K27me3 marks.
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Contributor(s) |
Curry EW, Brown R |
Citation missing |
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Submission date |
Dec 11, 2017 |
Last update date |
Mar 25, 2019 |
Contact name |
Ed Curry |
E-mail(s) |
e.curry@imperial.ac.uk
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Organization name |
Imperial College London
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Street address |
Hammersmith Hospital, Du Cane Road
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City |
London |
ZIP/Postal code |
W12 0NN |
Country |
United Kingdom |
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Platforms (1) |
GPL570 |
[HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array |
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Samples (4)
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GSM2883486 |
Patient 1 serous epithelial ovarian carcinoma |
GSM2883487 |
Patient 2 serous epithelial ovarian carcinoma |
GSM2883488 |
Patient 3 serous epithelial ovarian carcinoma |
GSM2883489 |
Patient 4 serous epithelial ovarian carcinoma |
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This SubSeries is part of SuperSeries: |
GSE107931 |
Bivalent chromatin domains in ovarian tumours at initial presentation identify genes predisposed to DNA hypermethylation during acquired resistance to chemotherapy |
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Relations |
BioProject |
PRJNA434271 |