Current smoking-specific gene expression signature in normal bronchial epithelium is enhanced in squamous cell lung cancer

被引:57
作者
Boelens, Mirjam C. [2 ]
van den Berg, Anke [2 ]
Fehrmann, Rudolf S. N. [3 ]
Geerlings, Marie [2 ]
de Jong, Wouter K.
Meerman, Gerard J. te [3 ]
Sietsma, Hannie [2 ]
Timens, Winn [2 ]
Postma, Dirkje S.
Groen, Harry J. M. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Pulmonol, NL-9713 GZ Groningen, Netherlands
[2] Univ Med Ctr Groningen, Dept Pathol, Groningen, Netherlands
[3] Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands
关键词
smoking; bronchial epithelium; squamous cell lung carcinoma; laser microdissection; microarray; TUMOR-SUPPRESSOR GENE; DYNEIN HEAVY-CHAIN; AIRWAY EPITHELIUM; 2-COLOR MICROARRAYS; CIGARETTE SMOKERS; PROTEIN; CARCINOMA; GLUCOCORTICOIDS; OVEREXPRESSION; IDENTIFICATION;
D O I
10.1002/path.2520
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Cigarette smoking is the main risk factor for the development of squamous cell lung carcinoma (SCC). However, the smoking-related molecular changes in SCC have not been studied. Gene expression studies in both histologically normal bronchial epithelium and SCC epithelial samples identified genes differentially expressed between current and ex-smokers. Subsequently, expression levels of the smoking-related genes in normal bronchial epithelium were compared with those in SCC cells, since we hypothesized that the smoking-induced changes would be also deregulated in SCC. Gene expression profiles were generated using Agilent whole human genome microarrays on laser-microdissected normal bronchial epithelium and SCC samples. Expression levels of 246 genes, mainly related to oxidative stress response, were significantly different between normal bronchial epithelium of current and ex-smokers. Such a differential gene expression profile did not exist in SCC cells of smokers and ex-smokers. Interestingly, when comparing SCC and normal bronchial epithelium from ex-smokers, the vast majority of these 246 genes were also deregulated in SCC. When comparing SCC with normal epithelium from smokers, 22% of the up-regulated genes showed a similar high expression in SCC whereas 79% of the down-regulated genes were even further reduced in SCC as compared to current smokers. The down-regulated genes included several tumour suppressor genes, such as C9orf9, INHBB, LRIG1, SCGB3A1, SERPINI2, STEAP3 and ZMYND10. Thus, our study shows that the majority of genes up-regulated in normal bronchial epithelium of current smokers show similar high expression levels in SCC, while down-regulated genes are even further repressed in SCC. Our data indicate that smoking-related changes in normal bronchial epithelial cells persist in malignant transformed squamous cells. Copyright (c) 2009 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:182 / 191
页数:10
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