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Status |
Public on Nov 22, 2011 |
Title |
Proteasome inhibition blocks estrogen-dependent gene transcription by decreasing histone H2B monoubiquitination in human breast cancer cells |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
The estrogen receptor-alpha (ERα) determines breast cancer cell phenotype and is a prognostic indicator. A better understanding of the mechanisms controlling ERα function may uncover improved strategies for the treatment of breast cancer. Proteasome inhibition was previously reported to regulate estrogen-induced transcription but the mechanisms by which it influences ERα function remain controversial. In this study we investigated the transcriptome-wide effects of the proteasome inhibitor Velcade on estrogen-regulated transcription in MCF7 human breast cancer cells and demonstrate a specific global decrease in estrogen-induced transcription.
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Overall design |
This set contains 12 microarray samples. 3 controls, 3 estrogen stimulated, 3 Bortezomib stimulated, 3 Bortezomib + estrogen stimulated
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Contributor(s) |
Prenzel T, Begus-Nahrmann Y, Kramer F, Hennion M, Hsu C, Gorsler T, Hintermayr C, Eick D, Kremmer E, Simons M, Beissbarth T, Johnsen SA |
Citation(s) |
21862633 |
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Submission date |
Jul 25, 2011 |
Last update date |
Aug 13, 2018 |
Contact name |
Frank Kramer |
E-mail(s) |
frank.kramer@med.uni-goettingen.de
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Organization name |
University Medical Center Göttingen
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Department |
Department of Medical Statistics
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Street address |
Humboldtallee 32
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City |
Goettingen |
ZIP/Postal code |
37073 |
Country |
Germany |
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Platforms (1) |
GPL10558 |
Illumina HumanHT-12 V4.0 expression beadchip |
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Samples (12)
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Relations |
BioProject |
PRJNA146281 |