NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM512565 Query DataSets for GSM512565
Status Public on Jun 01, 2010
Title histologically normal breast epithelium from ER+ breast cancer patient sample 9
Sample type RNA
 
Source name Histologically Normal Epithelium from ER+ Breast Cancer Patient
Organism Homo sapiens
Characteristics specimen: ER+ Breast Cancer
disease state: breast cancer
tissue: breast epithelium
Treatment protocol Tissues were snap frozen, embedded in OCT, sectioned at 10μm, stained with diluted hematoxylin and eosin (H&E) and then NlEpi – both TDLUs and ducts - was microdissected. Most HN samples were “tumor-adjacent” (i.e., located 1-2 cm from the tumor, on blocks lacking malignant cells. Some HN lay further away, but still in the same quadrant as the tumor, since most surgeries were lumpectomies. Great care was taken to avoid microdissecting any proliferative cells, even simple hyperplastic lesions.
Extracted molecule total RNA
Extraction protocol RNA was extracted from the microdissected cells using the PicoPure extraction kit (Molecular Devices, Sunnyvale, CA).
Label Biotin
Label protocol T7-based RNA amplification was performed on 100 ng of RNA using the MessageAmp aRNA kit from Ambion (Austin, TX). For second round amplification, cDNA for each sample was in vitro transcribed (IVT) to biotin-labeled cRNA with the IVT labeling kit (Affymetrix, Santa Clara, CA).
 
Hybridization protocol 10 µg of fragmented cRNA and hybridization controls were hybridized to each U133A GeneChip (Affymetrix) for 16 hours and then washed and stained according to the standard antibody amplification for eukaryotic targets protocol (Affymetrix)
Scan protocol The stained arrays were scanned using a G2500 Scanner (Agilent)
Description Gene Expression data from case 232H:Histologically Normal Epithelium from ER+ Breast Cancer Patient
Data processing .cel files were processed with MAS 5.0 using standard procedures for quality control and normalization was limited to rescaling each sample to a mean intensity of 200.
 
Submission date Feb 19, 2010
Last update date May 31, 2013
Contact name Kelly Graham
Organization name Boston University School of Medicine
Department Hematology/Oncology
Lab Rosenberg
Street address 650 Albany Street
City Boston
State/province MA
ZIP/Postal code 02118
Country USA
 
Platform ID GPL96
Series (2)
GSE20437 Histologically normal epithelium from breast cancer patients and cancer-free prophylactic mastectomy patients
GSE21947 Gene expression profiles of breast cancer subtypes are detectable in histologically normal breast epithelium
Relations
Reanalyzed by GSE47561

Data table header descriptions
ID_REF
VALUE MAS 5.0 signal intensity
ABS_CALL
DETECTION P-VALUE

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
1007_s_at 3233.1 P 0.000388
1053_at 47.6 A 0.150527
117_at 107.6 A 0.081337
121_at 877.4 P 0.006532
1255_g_at 82.1 A 0.089405
1294_at 980.8 P 0.000468
1316_at 176.3 P 0.00418
1320_at 8.8 A 0.781017
1405_i_at 26.5 A 0.216313
1431_at 58 A 0.162935
1438_at 25.8 A 0.621816
1487_at 370.5 P 0.039365
1494_f_at 263.9 P 0.003067
1598_g_at 2172 P 0.000322
160020_at 345.1 P 0.031336
1729_at 509.5 P 0.000562
177_at 87.7 A 0.107301
1773_at 20.8 A 0.660442
179_at 373.2 P 0.024711
1861_at 94.7 A 0.127645

Total number of rows: 22283

Table truncated, full table size 593 Kbytes.




Supplementary file Size Download File type/resource
GSM512565_232H.CEL.gz 2.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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