Biomarker Discovery in Non―Small Cell Lung Cancer: Integrating Gene Expression Profiling, Meta-analysis, and Tissue Microarray Validation

Global gene expression profiling has been widely used in lung cancer research to identify clinically relevant molecular subtypes as well as to predict prognosis and therapy response. So far, the value of these multigene signatures in clinical practice is unclear, and the biologic importance of indiv...

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Veröffentlicht in:Clinical cancer research 2013, Vol.19 (1), p.194-204
Hauptverfasser: BOTLING, Johan, EDLUND, Karolina, KÖNIG, André, FERNANDES, Oswaldo, KARLSSON, Mats, HELENIUS, Gisela, KARLSSON, Christina, RAHNENFÜHRER, Jörg, HENGSTLER, Jan G, MICKE, Patrick, LOHR, Miriam, HELLWIG, Birte, HOLMBERG, Lars, LAMBE, Mats, BERGLUND, Anders, EKMAN, Simon, BERGQVIST, Michael, PONTEN, Fredrik
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Sprache:eng
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Zusammenfassung:Global gene expression profiling has been widely used in lung cancer research to identify clinically relevant molecular subtypes as well as to predict prognosis and therapy response. So far, the value of these multigene signatures in clinical practice is unclear, and the biologic importance of individual genes is difficult to assess, as the published signatures virtually do not overlap. Here, we describe a novel single institute cohort, including 196 non-small lung cancers (NSCLC) with clinical information and long-term follow-up. Gene expression array data were used as a training set to screen for single genes with prognostic impact. The top 450 probe sets identified using a univariate Cox regression model (significance level P < 0.01) were tested in a meta-analysis including five publicly available independent lung cancer cohorts (n = 860). The meta-analysis revealed 14 genes that were significantly associated with survival (P < 0.001) with a false discovery rate
ISSN:1078-0432
1557-3265
1557-3265
DOI:10.1158/1078-0432.ccr-12-1139