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Series GSE45202 Query DataSets for GSE45202
Status Public on Mar 16, 2013
Title Amplitude modulation of androgen signaling by c-MYC [RNA-Seq]
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Androgen-stimulated growth of the molecular apocrine breast cancer is mediated by an androgen receptor (AR)-regulated transcriptional program. Through profiling the genomic licalizations of AR and its co-regulators FOXA1 and TCF7L2 in MDA-MB-453 breast cancer cells, we revealed the molecular details of the AR-centered regulatory network. We further identified that c-MYC is a key downstream target co-regulated by AR, FOXA1 and TCF7L2, and reinforces the transctiopnal activation of androgen-responsive genes in this subtype of breast cancers.
 
Overall design MDA-MB-453 breast cancer cells were transfected with control of MYC siRNA for 48 h, followed by treatment with 10nM DHT or vehicle for 6 h. The cells were subjected to mRNA purification and library praparation for RNA-seq on Illumina HiSeq2000 platform.
 
Contributor(s) Ni M, Fei T, Chen Y, Brown M
Citation(s) 23530127
Submission date Mar 15, 2013
Last update date May 15, 2019
Contact name Yiwen Chen
E-mail(s) ychen26@mdanderson.org
Organization name University of Texas MD Anderson Cancer Center
Department Bioinformatics and Computational Biology
Lab Yiwen Chen
Street address 1400 Pressler Street
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platforms (1)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (3)
GSM1099035 MDA-MB-453 siCtrl-veh
GSM1099036 MDA-MB-453 siCtrl-DHT
GSM1099037 MDA-MB-453 siMYC-DHT
This SubSeries is part of SuperSeries:
GSE45203 Amplitude modulation of androgen signaling by c-MYC
Relations
BioProject PRJNA193203
SRA SRP019498

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Supplementary file Size Download File type/resource
GSE45202_Cuffdiff_on_siCtrl_veh_vs_SiMYC_DHT_transcript_FPKM_tracking.tab.gz 1.2 Mb (ftp)(http) TAB
GSE45202_Cuffdiff_on_siCtrl_veh_vs_siCtrl_DHT_transcript_FPKM_tracking.tab.gz 1.2 Mb (ftp)(http) TAB
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Raw data are available in SRA
Processed data are available on Series record

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