Baseline gene expression predicts sensitivity to gefitinib in non-small cell lung cancer cell lines.

Coldren CD, Helfrich BA, Witta SE, Sugita M, Lapadat R, Zeng C, BarĂ³n A, Franklin WA, Hirsch FR, Geraci MW, Bunn PA
Mol Cancer Res. 2006 4 (8): 521-8

PMID: 16877703 · DOI:10.1158/1541-7786.MCR-06-0095

Tyrosine kinase inhibitors (TKI) of the epidermal growth factor receptor (EGFR) produce objective responses in a minority of patients with advanced-stage non-small cell lung cancer (NSCLC), and about half of all treated patients progress within 6 weeks of instituting therapy. Because the target of these agents is known, it should be possible to develop biological predictors of response, but EGFR protein levels have not been proven useful as a predictor of TKI response in patients and the mechanism of primary resistance is unclear. We used microarray gene expression profiling to uncover a pattern of gene expression associated with sensitivity to EGFR-TKIs by comparing NSCLC cell lines that were either highly sensitive or highly resistant to gefitinib. This sensitivity-associated expression profile was used to predict gefitinib sensitivity in a panel of NSCLC cell lines with known gene expression profiles but unknown gefitinib sensitivity. Gefitinib sensitivity was then determined for members of this test panel, and the microarray-based sensitivity prediction was correct in eight of nine NSCLC cell lines. Gene and protein expression differences were confirmed with a combination of quantitative reverse transcription-PCR, flow cytometry, and immunohistochemistry. This gene expression pattern related to gefitinib sensitivity was independent from sensitivity associated with EGFR mutations. Several genes associated with sensitivity encode proteins involved in HER pathway signaling or pathways that interrelate to the HER signaling pathway. Some of these genes could be targets of pharmacologic interventions to overcome primary resistance.

MeSH Terms (24)

Antineoplastic Agents Cadherins Carcinoma, Non-Small-Cell Lung Cluster Analysis Drug Screening Assays, Antitumor ErbB Receptors Flow Cytometry Gefitinib Gene Expression Gene Expression Profiling Humans Inhibitory Concentration 50 Lung Neoplasms Multigene Family Mutation Polymerase Chain Reaction Protein Kinase Inhibitors Proteome Proto-Oncogene Proteins Proto-Oncogene Proteins p21(ras) Quinazolines ras Proteins Treatment Outcome Tumor Cells, Cultured

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