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Sample GSM1070626 Query DataSets for GSM1070626
Status Public on Jan 30, 2013
Title MCF-7aro (AD + Letrozole) replicate 1
Sample type RNA
 
Source name cell population of MCF-7 stably transfected with the human placental aromatase gene sensitive to letrozole (MCF-7aro cells)
Organism Homo sapiens
Characteristics cell line: MCF-7
Treatment protocol Prior to experiment, cells were purged in Dulbecco’s Modified Eagle Medium without phenol red, supplemented with 3% steroid-depleted, dextran-coated and charcoal-treated fetal calf serum (DCC medium) for 4 days. MCF-7aro and Res-Let cells were then grown for 4 days in the presence of 25 nM of androstenedione combined or not with 10-6 M of letrozole. Media and treatment were changed every 2 days.
Growth protocol Cells were grown in DMEM medium supplemented with 10% fetal bovine serum
Extracted molecule total RNA
Extraction protocol Total RNA from cell culture was prepared using the miRNeasy Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer’s recommendations and subsequently quantified on a Nanodrop ND1000 spectrophotometer (Nanodrop Technologies, Wilmington, DE, USA). RNA integrity was checked using the BioAnalyzer 2100 (Agilent Technologies, Palo Alto, CA, USA).
Label biotin
Label protocol Complex probes were produced from total RNA using the FlashTag™ Biotin HSR RNA labeling kit (Affymetrix, Santa Clara, CA, USA)
 
Hybridization protocol Complex probes were hybridized to each GeneChip® miRNA 3.0 array according to the manufacturer's recommendations (Affymetrix).
Scan protocol GeneChips were scanned using the GeneChip Scanner 3000.
Description miRNA expression data from cell population of MCF-7aro treated in the presence of 25 nM of androstenedione and 10-6M of letrozole, cell culture replicate 1
Data processing Scanned images of microarray chips were analyzed using Expression Console (Affymetrix) with the default settings. Raw data were processed using different algorithms. Detected Above Background algorithm (DABD) and RMA Background Adjustment algorithm were performed in order to remove the background value.
 
Submission date Jan 25, 2013
Last update date Jan 30, 2013
Contact name Julie A Vendrell
E-mail(s) julie.vendrell@univ-lyon1.fr
Organization name ISPBL - Faculté de Pharmacie de Lyon
Department INSERM U1052
Lab Centre de Recherche en Cancérologie de Lyon
Street address 8 avenue Rockefeller
City Lyon
State/province Select a State or Province
ZIP/Postal code 69008
Country France
 
Platform ID GPL16384
Series (1)
GSE43766 identification of miRNA differential expression patterns in a new model of acquired letrozole resistance

Data table header descriptions
ID_REF
VALUE RMA signal intensity

Data table
ID_REF VALUE
14q0_st -0.006210923
14qI-1_st 0.3977267
14qI-1_x_st 0.03140178
14qI-2_st 0.5836163
14qI-3_x_st 0.1333222
14qI-4_st 0.1658944
14qI-4_x_st 0.2560045
14qI-5_st 0.4663513
14qI-6_st 0.3142264
14qI-6_x_st 0.2560045
14qI-7_st 0.4145289
14qI-8_st 0.1900607
14qI-8_x_st 0.1447426
14qI-9_x_st 0.2682035
14qII-10_st 0.4672756
14qII-10_x_st 0.2560045
14qII-11_st 0.1766295
14qII-11_x_st 0.6954959
14qII-12_st 0.2181767
14qII-12_x_st 0.3451503

Total number of rows: 25015

Table truncated, full table size 656 Kbytes.




Supplementary file Size Download File type/resource
GSM1070626_MCF-7aro_AD_Let_1.CEL.gz 760.9 Kb (ftp)(http) CEL
Processed data included within Sample table

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