Gene Expression-Based Classification of Non-Small Cell Lung Carcinomas and Survival Prediction

被引:629
作者
Hou, Jun [1 ]
Aerts, Joachim
den Hamer, Bianca [1 ]
van IJcken, Wilfred [2 ]
den Bakker, Michael
Riegman, Peter
van der Leest, Cor
van der Spek, Peter
Foekens, John A. [1 ]
Hoogsteden, Henk C.
Grosveld, Frank [1 ]
Philipsen, Sjaak [1 ]
机构
[1] Erasmus Univ, Med Ctr, Canc Genom Ctr, Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Ctr Biom, Rotterdam, Netherlands
来源
PLOS ONE | 2010年 / 5卷 / 04期
关键词
GROWTH-FACTOR RECEPTOR; CANCER; ADENOCARCINOMA; MICROARRAYS; IDENTIFICATION; SIGNATURE; PROFILES; EGFR;
D O I
10.1371/journal.pone.0010312
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Current clinical therapy of non-small cell lung cancer depends on histo-pathological classification. This approach poorly predicts clinical outcome for individual patients. Gene expression profiling holds promise to improve clinical stratification, thus paving the way for individualized therapy. Methodology and Principal Findings: A genome-wide gene expression analysis was performed on a cohort of 91 patients. We used 91 tumor-and 65 adjacent normal lung tissue samples. We defined sets of predictor genes (probe sets) with the expression profiles. The power of predictor genes was evaluated using an independent cohort of 96 non-small cell lung cancer-and 6 normal lung samples. We identified a tumor signature of 5 genes that aggregates the 156 tumor and normal samples into the expected groups. We also identified a histology signature of 75 genes, which classifies the samples in the major histological subtypes of non-small cell lung cancer. Correlation analysis identified 17 genes which showed the best association with post-surgery survival time. This signature was used for stratification of all patients in two risk groups. Kaplan-Meier survival curves show that the two groups display a significant difference in post-surgery survival time (p = 5.6E-6). The performance of the signatures was validated using a patient cohort of similar size (Duke University, n = 96). Compared to previously published prognostic signatures for NSCLC, the 17 gene signature performed well on these two cohorts. Conclusions: The gene signatures identified are promising tools for histo-pathological classification of non-small cell lung cancer, and may improve the prediction of clinical outcome.
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页数:12
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