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Status |
Public on Nov 30, 2012 |
Title |
Expression data of EZH2-dependent genes in prostate cancer cell lines |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by array
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Summary |
EZH2 is frequently over-expressed in aggressive and metastatic solid tumors, including castration resistant prostate cancer (CRPC). We sought to determine EZH2-dependent gene expression programmes in prostate cancer progression, and found an intriguing functional switch of EZH2 from a repressor to an activator during CRPC development. We used microarrays to detail the global profiling of gene expression that are differentially regulated upon EZH2 depletion in two different prostate cancer cell lines.
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Overall design |
The androgen-dependent prostate cancer cell line LNCaP and the LNCaP-derived androgen-independent cell line LNCaP-abl (abl) were used for this study, as their transcription profiles strongly resemble that of clinical androgen-dependent and castration resistant prostate tumors, respectively. EZH2 was silenced by specific siRNAs in both cell lines, and total RNA was extracted and hybridized on Affymetrix microarrays.
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Contributor(s) |
Xu K, Wu ZJ |
Citation(s) |
23239736 |
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Submission date |
Jul 18, 2012 |
Last update date |
Mar 25, 2019 |
Contact name |
Kexin Xu |
E-mail(s) |
kxuthscsa@gmail.com
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Organization name |
UT Health Science Center at San Antonio
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Department |
Molecular Medicine
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Street address |
7703 Floyd Curl, MC 8257
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City |
San Antonio |
State/province |
TX |
ZIP/Postal code |
78229 |
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: |
GSE39461 |
Role of PRC2 complex components in prostate cancer cell lines |
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Relations |
BioProject |
PRJNA170907 |