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Status |
Public on Oct 25, 2012 |
Title |
LM318 |
Sample type |
RNA |
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Source name |
BATTLE_trial_core biopsy_chemorefractory non-small cell lung cancer
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Organism |
Homo sapiens |
Characteristics |
egfr mutation: WT kras mutation: WT egfr index: 0.32
|
Treatment protocol |
Samples were OCT-embedded and frozen before RNA extraction
|
Growth protocol |
Core biopsies from patients included in the Biomarker-integrated Approaches of Targeted Therapy for Lung Cancer Elimination (BATTLE)
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Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted and purified from OCT-embedded tissue using the RNeasy Mini Kit (Qiagen) including on-column DNase (Qiagen) digestion as described by the manufacturer's protocol.
|
Label |
biotin
|
Label protocol |
RNA amplifications were performed using the WT-Amplification™ Pico (NuGEN) kit. For all experiments, the manufacturers' protocols were strictly followed. WT-Ovation™ Pico products (NuGEN) are labeled using the FL-Ovation™ cDNA Biotin Module V2 (NuGEN). Each labeled cRNA targets are synthesized according to manufacturer's protocols. The quantity and quality of the amplified cRNA or cDNA were assessed by a ND-1000 spectrophotometer (Nanodrop Technologies), and Agilent Bioanalyzer (Agilent Technologies), respectively.
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Hybridization protocol |
Hybridization mixtures were prepared according to Affymetrix procedures to accommodate 5 μg of cDNA targets from NuGEN amplification. Human Gene 1.ST platform were hybridized, revealed and washed according to the Affymetrix protocol.
|
Scan protocol |
Gene chips were scanned using a 7 G scanner (Affymetrix) and images (DAT files) were converted to CEL files using GCOS software (Affymetrix).
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Description |
LM001_525_AGE_1_LM318_01_22_09 Inclusion number in the clinical trial : 219
|
Data processing |
Raw data of microarrays were processed using quantile normalization and RMA algorithm (RMAExpress); expression values were log2 transformed
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Submission date |
Sep 02, 2011 |
Last update date |
Oct 25, 2012 |
Contact name |
Pierre Saintigny |
E-mail(s) |
psaintig@mdanderson.org
|
Organization name |
The University of Texas M.D. Anderson Cancer Center
|
Department |
Thoracic / Head and Neck Medical Oncology
|
Street address |
1515 Holcombe
|
City |
Houston |
ZIP/Postal code |
77030 |
Country |
USA |
|
|
Platform ID |
GPL6244 |
Series (2) |
GSE31852 |
An EGFR-mutation signature reveals features of the EGFR-dependent phenotype and identifies MACC1 as an EGFR-associated regulator of MET. |
GSE33072 |
An epithelial-mesenchymal transition (EMT) gene signature predicts resistance to erlotinib and PI3K pathway inhibitors and identifies Axl as a novel EMT marker in non-small cell lung cancer. |
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