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Sample GSM425918 Query DataSets for GSM425918
Status Public on Dec 13, 2011
Title G206-lcm
Sample type RNA
 
Source name PS_IB_3_asian_lcm
Organism Homo sapiens
Characteristics race: asian
age (years): unknown
stage: IB
grade: 3
histology: papillary serous
Treatment protocol Laser Capture microscopy was used to dissect cancer cell from tumors or epithelium from normal endometria to provide material for RNA extractions. Approximately 5-8 slides (with tissue samples 10 microns thick) of LCM microdissection were required for each cancer case and 20 slides of LCM were required for each normal. Cancer samples were microdissected to provide >95% purity of cancer. Normal endometria were dissected to provide >95% purity of normal epithelial cells.
Growth protocol Fresh frozen cancer specimens from 91 stage I endometrial patients were examined. Normal endometrial samples from twelve age matched postmenopausal women were used for comparison. All tissues were collected under an IRB approved protocol at the corresponding institutions. Specimens were harvested by pathologists and frozen within one hour of excision and each uterine tumor was frozen until the time of analysis. Tissue specimens were evaluated by one of two board certified gynecologic pathologists using H&E staining to confirm the diagnosis.
Extracted molecule total RNA
Extraction protocol Approximately 50ng of Total RNA was extracted from each sample with the Qiagen RNeasy® Micro Kit (Qiagen, 2003) by the manufacters suggested protocol for Total RNA Isolation from Microdissected Cryosections. See Rneasy® Micro Handbook Qiagen 4/2003.
Label biotin
Label protocol Extracted RNA was processed using the GeneChip two cycle cDNA synthesis kit (Affymetrix), see Chapter 2 of Gene Chip® Expression Technical Manual (2005-2009 Affymetrix, Inc.) for protocol.
 
Hybridization protocol Labeled RNAs were hybridized according to manufacterer's specifications (Affymetrix) for the HG-U133 plus 2.0 Gene Chip system, see Chapter 3 of Gene Chip® Expression Technical Manual (2005-2009 Affymetrix, Inc) for protocol.
Scan protocol Hybridized samples were washed, stained and scanned according to manufacterer's specifications (Affymetrix) for the HG-U133 plus 2.0 Gene Chip system, see protocol in GeneChip® Expression Wash, Stain and Scan User Manual.
Description End Ca_frozen_LCM
Data processing All expression data were normalized to a target intensity of 500 using Affymetrix's MAS5.0 algorithm. Affymetrix .CEL files were processed with the program GCOS to generate signal valuses. All .CEL files were scaled to a global median intensity target intensity of 500. Hieracrchical clustering of samples was performed with Cluster 3.0 and the dendograms were visualized with Tree View (Eisen Lab, University of California, Berkeley). Clustering was performed with the entire gene list (unsupervised) to determine wheter there are groupings of samples and the same software was used to generate heat maps of the most differentially expressed genes. Differential gene expression betweeen groups of samples was performed using BRB array tools from the National Cancer Institute (http://linus.nci.nih.gov/BRB-ArrayTools.html). The biological annotation of differentially expressed gene lists were carried out by a number of methods including DAVID (http://david.abcc.ncifcrf.gov/), IPA (Ingenuity Systems, Redwood City, CA) and MetaCore (GeneGo, San Diego, CA).
 
Submission date Jul 09, 2009
Last update date Dec 13, 2011
Contact name Uma Chandran
E-mail(s) [email protected]
Phone 412-648-9326
Organization name University of Pittsburgh
Department BioMedical Informatics
Street address 5150 Center Ave
City Pittsburgh
State/province PA
ZIP/Postal code 15232
Country USA
 
Platform ID GPL570
Series (1)
GSE17025 Gene Expression Analysis of Stage I Endometrial Cancers

Data table header descriptions
ID_REF
VALUE MAS5.0 Signal

Data table
ID_REF VALUE
1007_s_at 1982.9
1053_at 699.8
117_at 257.1
121_at 22345.7
1255_g_at 76.7
1294_at 462.7
1316_at 283.8
1320_at 33.7
1405_i_at 1337.5
1431_at 50.4
1438_at 65.5
1487_at 430.8
1494_f_at 175.2
1552256_a_at 470.7
1552257_a_at 1155.7
1552258_at 103.2
1552261_at 618.4
1552263_at 600.6
1552264_a_at 142.8
1552266_at 11.1

Total number of rows: 54675

Table truncated, full table size 867 Kbytes.




Supplementary file Size Download File type/resource
GSM425918.CEL.gz 4.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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