NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM602660 Query DataSets for GSM602660
Status Public on Sep 26, 2011
Title MCF-7ADR_multi-step_doxorubicin_selected_subline_rep_1
Sample type RNA
 
Source name MCF 7 cell line drug resistant cell subline
Organism Homo sapiens
Characteristics cell line: MCF7-ADR
treatment: Multi-step doxorubicin-selected subline
Biomaterial provider Dr. Kapil Mehta (MD Anderson Cancer Center, Houston, TX)
Treatment protocol MCF-7 cells were maintained in DMEM supplemented with 10 percent fetal calf serum, penicillin (100 units/mL), and streptomycin (100 ug/ml)
Extracted molecule total RNA
Extraction protocol RNA was isolated from approximately 1 million MCF-7 and MCF-7/ADR cells grown in two six-well plates. The medium and any detached cells were first removed from the wells, and total RNA was isolated from the cells that remained attached to the culture dish by use of the Qiagen RNeasy kit (Valencia, CA) by the manufacturers protocol. RNA was quantitated by use of a NanoDrop micro-volume spectrophotometer (Thermo Scientific, Wilmington, DE) and then the integrity of the mRNA was verified with an Agilent BioAnalyzer (Santa Clara, CA).
Label Biotin
Label protocol Isolated total RNA from the MCF-7 parental cells and MCF-7/ADR cells was used with the GeneChip Sample Cleanup Module to prepare biotinylated eukaryotic complementary RNA to hybridize to the GeneChip expression probe arrays, according to the manufacturers protocol (Qiagen).
 
Hybridization protocol The biotinylated complementary RNA was fragmented for 35 minutes at 94C in fragmentation buffer from the labelling kit (Enzo, Farmingdale, NY) and then hybridized to the Affymetrix GeneChip U133A 2.0 arrays (Santa Clara, CA) for 16 hours at 45C. Each probe array was then washed and stained before being scanned.
Scan protocol Each probe array was scanned twice with the GeneArray Scanner, according to the manufacturers procedures (Affymetrix, Santa Clara, CA).
Description Doxorubicin-selected subline biological replicate 1
Data processing The CEL files for hybridizations of the MCF-7/ADR cells and the MCF-7 cells were log2-transformed by use of RMA Express (Bioinformatics 2003 19(2):185-193 and Biostatistics 2003 4(2):249-264). Microarray data for the expression of 14,500 genes from MCF-7 and MCF-7/ADR were filtered with BRB-ArrayTools (version 3.8.0) (developed by Dr. Richard Simon and BRB-ArrayTools Development Team from the Biometric Research Branch at the National Cancer Institute, NIH, Bethesda, MD). The array data were filtered by use of the exclusion parameters, spot intensities that were less than 10 and genes with a P value for the log-ratio variation that was greater than .01, and a total of 4976 genes were identified for further analysis. These 4976 genes were clustered by use of the Euclidean distance and complete linkage (Supplementary Figure 1, available online). The resulting dendrogram indicated that, for all experimental conditions, the duplicate microarrays form clusters, suggesting that the results were reproducible. A two-sample t test (with random variance model) was used to perform a class comparison and determine the statistically significant genes expressed between the MCF-7 and MCF-7/ADR cells. The univariate test random variance model parameters were a equals 1.68165, b equals 14.3422, and Kolmogorov–Smirnov statistic equals 0.03998. The nominal statistical significance level of each univariate test was .001. The first 419 genes listed were statistically significant at the nominal .001 level in the univariate test with a spot intensity fold change of 10. Genes with a spot intensity fold increase of greater than 10 are shown in Supplementary Table 1 (available online), and genes with spot intensity fold decrease of greater than –10 are shown in Supplementary Table 2 (available online).
 
Submission date Sep 30, 2010
Last update date Sep 26, 2011
Contact name Suresh V. Ambudkar
E-mail(s) ambudkar@helix.nih.gov
Organization name National Cancer Institute, NIH
Lab Laboratory of Cell Biology
Street address 37 Convent Dr., Room 2120
City Bethesda
State/province MD
ZIP/Postal code 20892
Country USA
 
Platform ID GPL571
Series (1)
GSE24460 Prolonged Drug Selection of Breast Cancer Cells and Enrichment of Cancer Stem Cell Characteristics.

Data table header descriptions
ID_REF
VALUE RMA signal

Data table
ID_REF VALUE
1007_s_at 7.793519
1053_at 8.569627
117_at 4.424183
121_at 7.946599
1255_g_at 3.433884
1294_at 4.235847
1316_at 4.52995
1320_at 4.760158
1405_i_at 3.617245
1431_at 3.71242
1438_at 5.635629
1487_at 6.477438
1494_f_at 4.883353
1598_g_at 8.016233
160020_at 6.358207
1729_at 6.938977
1773_at 5.299346
177_at 4.537672
179_at 7.279217
1861_at 7.465649

Total number of rows: 22277

Table truncated, full table size 432 Kbytes.




Supplementary file Size Download File type/resource
GSM602660_MCF7226ng.CEL.gz 1.8 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap