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Status |
Public on Oct 25, 2012 |
Title |
LM132 |
Sample type |
RNA |
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Source name |
BATTLE_trial_core biopsy_chemorefractory non-small cell lung cancer
|
Organism |
Homo sapiens |
Characteristics |
egfr mutation: WT kras mutation: WT egfr index: -0.52 histology-iw revised: Adenocarcinoma egfr-iw type: No kras-iw mutation (yes/no): No gender: Male race: White stage_at_diagnosis: IV prior_tx_for_mets: 2 smoking_status: Former biopsy site (grouped): 1: Lung treatment: sorafenib markergroup: 3 8-week disease control (1=yes, 0=no): 0 randomization_date: 2008-02-26 date_of_progression: 23-Apr-08 pfsc (1=progressed; 0=not progressed): 1 pfsm (month): 1.8727
|
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. 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).
|
Description |
Human Gene 1.0 ST_525_LM_132_06_24_08 Inclusion number in the clinical trial : 143
|
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 |
Aug 16, 2011 |
Last update date |
Oct 25, 2012 |
Contact name |
Pierre Saintigny |
E-mail(s) |
[email protected]
|
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 (3) |
GSE31428 |
Final efficacy and biomarker analysis of the sorafenib arm of the BATTLE (Biomarker-Integrated Approaches of Targeted Therapy for Lung Cancer Elimination) trial |
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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