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Sample GSM1038656 Query DataSets for GSM1038656
Status Public on Mar 15, 2015
Title HCT116-OxPt_rep3
Sample type RNA
 
Source name HCT116 cell line, oxaliplatin resistant, replicate 3
Organism Homo sapiens
Characteristics tissue: Cell line, colon cancer derived
cell line: HCT116
treatment: Oxaliplatin
Growth protocol Three parental cell lines (HCT116, HT29 and LoVo) were exposed in vitro to gradually increasing concentrations of oxaliplatin or SN-38 for about nine months. Before cell harvest, parental and drug-resistant cell lines were cultured in drug-free growth medium (RPMI1640+Glutamax supplemented with 10% fetal bovine serum, Invitrogen) for two to three weeks.
Extracted molecule total RNA
Extraction protocol RNA was purified from each cell line in independent triplicates (three different passages). Following a wash with cold PBS, TRIzol Reagent (Invitrogen) was added and the cells were lysed on ice. The lysate was frozen at -80˚C for later purification of RNA. RNA was purified according to the manufacturer’s instructions with minor modifications (centrifugation for 4500 x g, with centrifugation times of 20 min for the phase separation and 15 min for the RNA precipitation).
Label Cy3
Label protocol Total RNA was separately converted into cDNA through reverse transcription, thereafter cRNA was transcribed with T7 RNA Polymerase. Labeled cRNA was coupled to a Cyanine 3-CTP fluorescent dye using the One-Color Microarray-Based Gene Expression Analysis, Low Input Quick Amp Labeling (version 6.5 protocol) (Agilent Technologies).
 
Hybridization protocol Cy3-labeled cRNA was hybridized to Agilent Human Gene Expression Microarrays (G4112F).
Scan protocol Microarrays were scanned using an Agilent DNA Microarray scanner (Agilent Technologies).
Description GE_06
Gene expression of cell line growing in drug-free medium
Data processing Microarray data processing was performed in R (www.r-project.org) using the Bioconductor bioinformatics software package (www.bioconductor.org). Data (gProcessedSignals) were loaded into R using the Limma package and normalized between arrays using quantile normalization. Probes were collapsed taking the median and expression values were log2 transformed.
 
Submission date Nov 19, 2012
Last update date Mar 16, 2015
Contact name Niels Frank Jensen
Organization name University of Copenhagen
Department Faculty of Health and Medical Sciences
Lab Pathobiology
Street address Dyrlaegevej 88, 1.
City Frederiksberg C
ZIP/Postal code 1870
Country Denmark
 
Platform ID GPL16297
Series (1)
GSE42387 Gene expression profiles of parental and chemotherapy-resistant colon cancer cell lines.

Data table header descriptions
ID_REF
VALUE Normalized, log2-transformed signal intensity.

Data table
ID_REF VALUE
A_23_P10060 6.327594226
A_23_P10091 7.376889092
A_23_P101121 7.5261007
A_23_P103951 10.77232985
A_23_P104012 6.735211253
A_23_P10525 6.425954063
A_23_P105732 12.00748805
A_23_P10605 9.210220361
A_23_P106814 8.357063204
A_23_P108534 6.904216461
A_23_P10987 8.87543651
A_23_P11119 6.507501022
A_23_P111766 11.35349912
A_23_P112957 6.772833842
A_23_P113056 6.499255345
A_23_P113101 6.57406786
A_23_P113263 8.28171542
A_23_P113453 6.534266852
A_23_P113692 5.992046634
A_23_P113762 6.319588499

Total number of rows: 32705

Table truncated, full table size 730 Kbytes.




Supplementary file Size Download File type/resource
GSM1038656_GE_06.txt.gz 2.2 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data are available on Series record

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