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Status |
Public on Dec 04, 2007 |
Title |
Response to estradiol-ERalpha |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
In addition to the estrogen responsive element (ERE)-dependent gene expression, E2-ERalpha regulates transcription through functional interactions with transfactors bound to their cognate regulatory elements on DNA, hence the ERE-independent signaling pathway. However, the relative importance of the ERE-independent pathway in E2-ERalpha signaling is unclear. Our studies in infected ER-negative cell models with an ERalpha demonstrated that genomic responses assessed by microarrays from the alter cellular growth, death or motility. Keywords: MDA-MB-231 cells
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Overall design |
Cells were infected with the recombinant adenovirus bearing no cDNA (CMV) or cDNA for ERalpha for 48h. Infected cells were then treated with 1 nM Estradiol 17beta for 6h. All experiments were repeated six independent times conducted at at six different days
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Contributor(s) |
Muyan M, Nott S, Huang Y |
Citation(s) |
19321454 |
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Submission date |
Dec 03, 2007 |
Last update date |
Mar 25, 2019 |
Contact name |
Stephen Welle |
E-mail(s) |
[email protected]
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Organization name |
University of Rochester
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Street address |
601 Elmwood Avenue
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City |
Rochester |
State/province |
NY |
ZIP/Postal code |
14642 |
Country |
USA |
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Platforms (1) |
GPL570 |
[HG-U133_Plus_2] Affymetrix Human Genome U133 Plus 2.0 Array |
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Samples (12)
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This SubSeries is part of SuperSeries: |
GSE9761 |
Response to estradiol-ERalpha, estradiol-Erbeta, and ERE Binding defective mutants |
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Relations |
BioProject |
PRJNA105105 |