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Series GSE41614 Query DataSets for GSE41614
Status Public on Mar 08, 2013
Title Transcriptional profiling of tumor-associated blood vessels in invasive bladder cancer
Organism Homo sapiens
Experiment type Expression profiling by array
Summary Tumor-associated blood vessels differ from normal vessels at the morphological and molecular level. Proteins that are only present on tumor vessels may serve as biomarkers and as therapeutic targets for inhibition of angiogenesis in cancer. Comparing the transcriptional profiles of blood vascular endothelium from human invasive bladder cancer and from normal bladder tissue, we found several markers that could serve as novel biomarkers or therapeutic targets.
In this dataset, we include the expression data obtained from laser capture microdissected (LCM) vessels isolated from tumor and bladder normal tissue.
 
Overall design 10 samples were analyzed. We compared expression of tumor associated blood vessels with expression of vessels in the normal bladder tissue using Genespring GX 12.
 
Contributor(s) Roudnicky F, Poyet C, Detmar M
Citation(s) 23243026
Submission date Oct 16, 2012
Last update date Feb 18, 2019
Contact name Filip Roudnicky
E-mail(s) filip.roudnicky@pharma.ethz.ch
Phone +41 44 633 73 14
Fax +41 44 633 13 64
Organization name Swiss Federal Institute of Technology
Department Institute of Pharmaceutical Sciences
Lab Pharmacogenomics
Street address Langwiesstrasse 25
City Zurich
ZIP/Postal code 8093
Country Switzerland
 
Platforms (1)
GPL5175 [HuEx-1_0-st] Affymetrix Human Exon 1.0 ST Array [transcript (gene) version]
Samples (10)
GSM1020196 isolated blood vessels from normal bladder; patient 6
GSM1020197 isolated blood vessels from bladder cancer; patient 6
GSM1020198 isolated blood vessels from normal bladder; patient 7
Relations
BioProject PRJNA177693

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SOFT formatted family file(s) SOFTHelp
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Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE41614_RAW.tar 203.2 Mb (http)(custom) TAR (of CEL)
Processed data included within Sample table

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