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Series GSE30034 Query DataSets for GSE30034
Status Public on Nov 16, 2011
Title Redefining the Relevance of Established Cancer Cell Lines to the Study of Clinical Anti-Cancer Drug Resistance
Organism Homo sapiens
Experiment type Expression profiling by RT-PCR
Summary Although in vitro models have been a cornerstone of anti-cancer drug development, their direct applicability to clinical cancer research has actually been uncertain. Using a state-of-the-art Taqman-based qRT-PCR assay, we investigated the multidrug resistance (MDR) transcriptome of six cancer types, in both in vitro and in vivo samples.
 
Overall design We studied 380 MDR genes, selected a priori based on an extensive curation of the literature published during the last three decades, in established cancer cell lines and clinical samples, either containing greater than 75% tumor cells or microdissected.
 
Contributor(s) Gillet J, Calcagno AM, Varma S, Marino M, Green L, Vora M, Patel C, Orina J, Eliseeva T, Singal V, Padmanabhan R, Davidson B, Ganapathi R, Sood A, Rueda B, Ambudkar SV, Gottesman MM
Citation(s) 22068913
Submission date Jun 16, 2011
Last update date Mar 23, 2012
Contact name jean-pierre gillet
E-mail(s) jean-pierre.gillet@unamur.be
Phone 003281724275
Organization name University of Namur
Department URPhyM
Lab LMCB
Street address 61 Rue de Bruxelles
City Namur
ZIP/Postal code 5000
Country Belgium
 
Platforms (2)
GPL13728 TaqMan qRT-PCR Homo sapiens Low-Density Array 380
GPL14924 TaqMan qRT-PCR Homo sapiens Low-Density Array 380 v 2
Samples (228)
GSM743324 Clinical sample, Colon-N1
GSM743325 Clinical sample, Colon-T1
GSM743326 Clinical sample, Colon-N2
Relations
BioProject PRJNA144059

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE30034_GSM839031_to_GSM839069_raw_Ct_values.txt.gz 22.9 Kb (ftp)(http) TXT
GSE30034_raw_Ct_values.txt.gz 120.5 Kb (ftp)(http) TXT
Processed data included within Sample table

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