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Cancer Prevention Research 1, 112, July 1, 2008. Published Online First March 31, 2008;
doi: 10.1158/1940-6207.CAPR-07-0017
© 2008 American Association for Cancer Research

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Research Articles

Impact of Smoking Cessation on Global Gene Expression in the Bronchial Epithelium of Chronic Smokers

Li Zhang1, J. Jack Lee1, Hongli Tang2, You-Hong Fan2, Lianchun Xiao1, Hening Ren2, Jonathan Kurie2, Rodolfo C. Morice2, Waun Ki Hong2 and Li Mao2

Authors' Affiliations: Departments of 1 Bioinformatics and Computational Biology and 2 Thoracic/Head and Neck Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas

Requests for reprints: Li Zhang, M. D. Anderson Cancer Center, Houston, TX 77030. E-mail: Lzhangli{at}mdanderson.org, or Li Mao, M. D. Anderson Cancer Center. E-mail: lmao{at}mdanderson.org.


Cigarette smoke is the major cause of lung cancer and can interact in complex ways with drugs for lung cancer prevention or therapy. Molecular genetic research promises to elucidate the biological mechanisms underlying divergent drug effects in smokers versus nonsmokers and to help in developing new approaches for controlling lung cancer. The present study compared global gene expression profiles (determined via Affymetrix microarray measurements in bronchial epithelial cells) between chronic smokers, former smokers, and never smokers. Smoking effects on global gene expression were determined from a combined analysis of three independent data sets. Differential expression between current and never smokers occurred in 591 of 13,902 measured genes (P < 0.01 and >2-fold change; pooled data)—a profound effect. In contrast, differential expression between current and former smokers occurred in only 145 of the measured genes (P < 0.01 and >2-fold change; pooled data). Nine of these 145 genes showed consistent and significant changes in each of the three data sets (P < 0.01 and >2-fold change), with eight being down-regulated in former smokers. Seven of the eight down-regulated genes, including CYP1B1 and three AKR genes, influence the metabolism of carcinogens and/or therapeutic/chemopreventive agents. Our data comparing former and current smokers allowed us to pinpoint the genes involved in smoking-drug interactions in lung cancer prevention and therapy. These findings have important implications for developing new targeted and dosing approaches for prevention and therapy in the lung and other sites, highlighting the importance of monitoring smoking status in patients receiving oncologic drug interventions.


Commentary

Genomics of Smoking Exposure and Cessation: Lessons for Cancer Prevention and Treatment
Trevor M. Penning and Caryn Lerman
Cancer Prevention Research 2008 1: 80-83. [Full Text] [PDF]



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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2008 by the American Association for Cancer Research.