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Status |
Public on Apr 08, 2016 |
Title |
Characterization of chromatin accessibility through the DNaseI hypersensitivity assay in breast cancer cells treated with either Dex or E2 |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
The estrogen receptor (ER), glucocorticoid receptor (GR), and forkhead box protein 1 (FoxA1) are significant factors in breast cancer progression. FoxA1 is well-established as a pioneer factor for steroid receptor recruitment to chromatin. Here we show that ER and GR have the ability to alter the genomic response of FoxA1 to specific binding sites within the genome. These findings alter the classical understood mechanism of FoxA1 establishing a dynamic transcription factor that can be regulated by hormones.
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Overall design |
We examined the ER and GR mediated affects on FoxA1 binding patterms
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Contributor(s) |
Swinstead EE, Baek S, Hager GL |
Citation(s) |
27062924 |
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Submission date |
Aug 20, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Songjoon Baek |
Organization name |
NCI / NIH
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Department |
CCR
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Lab |
LRBGE
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Street address |
41 Library Drive
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City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892 |
Country |
USA |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (12)
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This SubSeries is part of SuperSeries: |
GSE72252 |
DNaseI hypersensitivity assay and ER, GR, and FoxA1 binding patterns in breast cancer cells |
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Relations |
BioProject |
PRJNA293470 |
SRA |
SRP062678 |