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Sample GSM658202 Query DataSets for GSM658202
Status Public on Jun 02, 2011
Title siAP-2γ (First Base)-transfected MCF-7, 12h E2
Sample type RNA
 
Source name MCF-7 breast cancer cells
Organism Homo sapiens
Characteristics cell line: MCF-7
condition: siAP-2γ (First Base)-transfected MCF-7, E2
Treatment protocol ~400,000 cells were seeded in phenol red-free DMEM/F12 containing 5% charcoal stripped FBS (Hyclone) with penicillin, streptomycin and gentamycin. Within 24h after seeding, cells were transfected with NC or siRNA targeting AP-2γ (from Dharmacon and First Base). Transfection was repeated the next day to achieve double knockdown. After 96h from the first transfection, hormone-depleted cells were treated with E2 to a final concentration of 10 nM for 12h before harvesting for RNA. Cells treated with an equal volume vehicle, ETOH (ethanol) for 12h are used as controls.
Growth protocol MCF-7 breast cancer cells were maintained in DMEM (Invitrogen/Gibco) supplemented with 5% fetal bovine serum (FBS), penicillin, streptomycin, and gentamycin in a 37°C incubator with 5% CO2.
Extracted molecule total RNA
Extraction protocol RNA was harvested using Trizol reagent (Sigma) and purified according to manufacturer protocol in PureLink RNA Mini Kit (Invitrogen).
Label biotin
Label protocol Biotinylated cRNA were prepared from 500ng total RNA using Illumina TotalPrep-96 RNA Amplification Kit (Ambion).
 
Hybridization protocol 750ng of cRNA were hybridized to the Sentrix HumanRef-8 v3 Expression BeadChip Kit (Illumina) according to the manufacturer protocol.
Scan protocol BeadChips were scanned using the BeadArray Reader.
Description 4671881066_A, 4671881068_A, 4671881069_A
Data processing Raw data was analyzed using GeneSpring GX 11.0 software. Dataset was normalized using percentile shift normalization and baseline transformed to median of control samples.
Triplicates were generated for the experiment and analyses were performed using the average of the triplicates (after normalization). Raw data provided as supplementary file (filename: GSE26740_non-normalized.txt.gz)
 
Submission date Jan 20, 2011
Last update date Jun 02, 2011
Contact name SI KEE TAN
E-mail(s) tansk99@gis.a-star.edu.sg
Organization name Genomic Institute of Singapore
Department Cancer biology and Pharmacology
Street address 60 Biopolis Street #02-01 Genome
City Singapore
ZIP/Postal code Singapore 138672
Country Singapore
 
Platform ID GPL6883
Series (2)
GSE26740 Activator protein-2γ is a critical determinant of estrogen receptor interactome formation and gene transcription in breast cancer [expression]
GSE26741 Activator protein-2γ is a critical determinant of estrogen receptor interactome formation and gene transcription in breast cancer

Data table header descriptions
ID_REF
VALUE Averaged normalized intensity values derived from GeneSpring GX software

Data table
ID_REF VALUE
ILMN_1722532 0.09561475
ILMN_1708805 -0.33067313
ILMN_1672526 -0.110854626
ILMN_1703284 -0.44328165
ILMN_2185604 -0.06624484
ILMN_1785107 -0.032873154
ILMN_1689711 -0.070723616
ILMN_1782551 0.4285682
ILMN_1656040 0.00201726
ILMN_1715540 0.06267214
ILMN_2371280 -0.027218023
ILMN_1777550 -0.16082041
ILMN_1788239 0.047519524
ILMN_2148679 -0.14298718
ILMN_1656792 -0.022949615
ILMN_1803590 0.10508617
ILMN_1730765 0.054206926
ILMN_1671809 0.022711357
ILMN_1750625 -0.10464629
ILMN_1689814 -0.1810809

Total number of rows: 24526

Table truncated, full table size 599 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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