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Sample GSM152929 Query DataSets for GSM152929
Status Public on Jan 16, 2007
Title Metastatic prostate tumor samples in para aortic lymph node from patient FB561 FB561_1CU95C
Sample type RNA
 
Source name FB561_1C, metastatic prostate tumor samples in para aortic lymph node from patient FB561
Organism Homo sapiens
Characteristics Tissue: prostate tumor metastases in para aortic lymph node
Treatment protocol Specimens were received directly from the operating room. Samples (>500 mg) were excised and snap frozen in liquid nitrogen within 30 min of excision and stored at -80°C until extraction of RNA. Metastatic tumor samples were obtained from a warm autopsy program and processed similarly to primary tumors. An H&E stained frozen section of each sample was evaluated by a pathologist, to determine epithelial and stromal content and verify the presence of tumor in the sample. Dissection of the frozen tissue block was performed with the guidance of a marked H & E slide to minimize the presence of host tissue in the metastatic samples. All samples used in the study contained >80% tumor. Metastatic tumor samples were minced and divided into two equal portions to be extracted with the sample protocol used for each set of primary tumors.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with Qiagen Rneasy kit according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 15 ug of cRNA were hybridized for 16 hr at 45C on GeneChip HG-U95C array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000.
Description Gene expression data from metastatic prostate cancer
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 200.
 
Submission date Dec 22, 2006
Last update date Jan 16, 2007
Contact name Federico Alberto Monzon
E-mail(s) famonzon@tmhs.org
Organization name The Methodist Hospital
Department Pathology
Lab Molecular Diagnostics
Street address 6565 Fannin St, MS205
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platform ID GPL93
Series (2)
GSE6605 Expression data from Metastatic Prostate Tumor
GSE6919 Expression Data from Normal and Prostate Tumor Tissues

Data table header descriptions
ID_REF 12579
VALUE MAS5-calculated Signal intensity

Data table
ID_REF VALUE
48609_r_at 13.2
48610_at 1820.1
48612_at 2058.1
48613_at 19.3
48615_at 899
48617_at 565.2
48619_at 125.4
48620_at 2890.7
48622_at 48.5
48624_at 21.8
48626_at 367
48628_at 150.5
48629_s_at 484
48630_r_at 130.5
48631_at 288.2
48633_at 39.9
48634_at 84.8
48640_g_at 210.9
48643_r_at 58
48645_at 83.7

Total number of rows: 12579

Table truncated, full table size 180 Kbytes.




Supplementary file Size Download File type/resource
GSM152929.CEL.gz 2.6 Mb (ftp)(http) CEL

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