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Status |
Public on Jun 12, 2018 |
Title |
ChIP-Seq analysis of estrogen deprived MCF7 cells treated with H3B-5942 and standards of care compounds |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
The goal of this experiment was to interrogate the potential transcriptional impact of H3B-5942 by investigating its influence on genome-wide DNA-binding modes of ERa in MCF7 cells using chromatin immunoprecipitation followed by high-throughput DNA sequencing (ChIP-Seq). Affects of H3B-5942 on chromatin recruitment were compared to results from treatment with E2, 4-OHT, and fulvestrant.
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Overall design |
A total of 5 treatments were analyzed. These included H3B-5942, E2, reference compounds 4-OHT and fulvestrant, and DMSO as control. Material from two plates per treatment were pooled and then analyzed.
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Contributor(s) |
Furman C, Wu ZJ |
Citation missing |
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Submission date |
Jun 11, 2018 |
Last update date |
Mar 26, 2019 |
Contact name |
Zhenhua Wu |
E-mail(s) |
zhenhuawu75@gmail.com
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Phone |
6179592279
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Organization name |
H3 Biomedicine
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Street address |
300 Technology Square floor 5
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City |
Cambridge |
State/province |
MA |
ZIP/Postal code |
02139 |
Country |
USA |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (11)
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This SubSeries is part of SuperSeries: |
GSE115611 |
Discovery of Selective Estrogen Receptor Covalent Antagonists (SERCAs) for the treatment of ERa(WT) and ERa(MUT) breast cancer. |
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Relations |
BioProject |
PRJNA475564 |
SRA |
SRP150236 |