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Effect of active smoking on the human bronchial epithelium transcriptome

BACKGROUND: Lung cancer is the most common cause of cancer-related deaths. Tobacco smoke exposure is the strongest aetiological factor associated with lung cancer. In this study, using serial analysis of gene expression (SAGE), we comprehensively examined the effect of active smoking by comparing th...

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Autores principales: Chari, Raj, Lonergan, Kim M, Ng, Raymond T, MacAulay, Calum, Lam, Wan L, Lam, Stephen
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2001199/
https://www.ncbi.nlm.nih.gov/pubmed/17727719
http://dx.doi.org/10.1186/1471-2164-8-297
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author Chari, Raj
Lonergan, Kim M
Ng, Raymond T
MacAulay, Calum
Lam, Wan L
Lam, Stephen
author_facet Chari, Raj
Lonergan, Kim M
Ng, Raymond T
MacAulay, Calum
Lam, Wan L
Lam, Stephen
author_sort Chari, Raj
collection PubMed
description BACKGROUND: Lung cancer is the most common cause of cancer-related deaths. Tobacco smoke exposure is the strongest aetiological factor associated with lung cancer. In this study, using serial analysis of gene expression (SAGE), we comprehensively examined the effect of active smoking by comparing the transcriptomes of clinical specimens obtained from current, former and never smokers, and identified genes showing both reversible and irreversible expression changes upon smoking cessation. RESULTS: Twenty-four SAGE profiles of the bronchial epithelium of eight current, twelve former and four never smokers were generated and analyzed. In total, 3,111,471 SAGE tags representing over 110 thousand potentially unique transcripts were generated, comprising the largest human SAGE study to date. We identified 1,733 constitutively expressed genes in current, former and never smoker transcriptomes. We have also identified both reversible and irreversible gene expression changes upon cessation of smoking; reversible changes were frequently associated with either xenobiotic metabolism, nucleotide metabolism or mucus secretion. Increased expression of TFF3, CABYR, and ENTPD8 were found to be reversible upon smoking cessation. Expression of GSK3B, which regulates COX2 expression, was irreversibly decreased. MUC5AC expression was only partially reversed. Validation of select genes was performed using quantitative RT-PCR on a secondary cohort of nine current smokers, seven former smokers and six never smokers. CONCLUSION: Expression levels of some of the genes related to tobacco smoking return to levels similar to never smokers upon cessation of smoking, while expression of others appears to be permanently altered despite prolonged smoking cessation. These irreversible changes may account for the persistent lung cancer risk despite smoking cessation.
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spelling pubmed-20011992007-10-06 Effect of active smoking on the human bronchial epithelium transcriptome Chari, Raj Lonergan, Kim M Ng, Raymond T MacAulay, Calum Lam, Wan L Lam, Stephen BMC Genomics Research Article BACKGROUND: Lung cancer is the most common cause of cancer-related deaths. Tobacco smoke exposure is the strongest aetiological factor associated with lung cancer. In this study, using serial analysis of gene expression (SAGE), we comprehensively examined the effect of active smoking by comparing the transcriptomes of clinical specimens obtained from current, former and never smokers, and identified genes showing both reversible and irreversible expression changes upon smoking cessation. RESULTS: Twenty-four SAGE profiles of the bronchial epithelium of eight current, twelve former and four never smokers were generated and analyzed. In total, 3,111,471 SAGE tags representing over 110 thousand potentially unique transcripts were generated, comprising the largest human SAGE study to date. We identified 1,733 constitutively expressed genes in current, former and never smoker transcriptomes. We have also identified both reversible and irreversible gene expression changes upon cessation of smoking; reversible changes were frequently associated with either xenobiotic metabolism, nucleotide metabolism or mucus secretion. Increased expression of TFF3, CABYR, and ENTPD8 were found to be reversible upon smoking cessation. Expression of GSK3B, which regulates COX2 expression, was irreversibly decreased. MUC5AC expression was only partially reversed. Validation of select genes was performed using quantitative RT-PCR on a secondary cohort of nine current smokers, seven former smokers and six never smokers. CONCLUSION: Expression levels of some of the genes related to tobacco smoking return to levels similar to never smokers upon cessation of smoking, while expression of others appears to be permanently altered despite prolonged smoking cessation. These irreversible changes may account for the persistent lung cancer risk despite smoking cessation. BioMed Central 2007-08-29 /pmc/articles/PMC2001199/ /pubmed/17727719 http://dx.doi.org/10.1186/1471-2164-8-297 Text en Copyright © 2007 Chari et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chari, Raj
Lonergan, Kim M
Ng, Raymond T
MacAulay, Calum
Lam, Wan L
Lam, Stephen
Effect of active smoking on the human bronchial epithelium transcriptome
title Effect of active smoking on the human bronchial epithelium transcriptome
title_full Effect of active smoking on the human bronchial epithelium transcriptome
title_fullStr Effect of active smoking on the human bronchial epithelium transcriptome
title_full_unstemmed Effect of active smoking on the human bronchial epithelium transcriptome
title_short Effect of active smoking on the human bronchial epithelium transcriptome
title_sort effect of active smoking on the human bronchial epithelium transcriptome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2001199/
https://www.ncbi.nlm.nih.gov/pubmed/17727719
http://dx.doi.org/10.1186/1471-2164-8-297
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