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Cancer Research 67, 5103, June 1, 2007. doi: 10.1158/0008-5472.CAN-07-0279
© 2007 American Association for Cancer Research

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Priority Reports

Mainstream Tobacco Smoke Causes Paternal Germ-Line DNA Mutation

Carole L. Yauk1, M. Lynn Berndt1, Andrew Williams2, Andrea Rowan-Carroll1, George R. Douglas1 and Martin R. Stämpfli3

1 Mutagenesis Section, Environmental and Occupational Toxicology Division; 2 Biostatistics and Epidemiology Division, Health Canada, Ottawa, Ontario, Canada; and 3 Department of Pathology and Molecular Medicine, Centre for Gene Therapeutics and Department of Medicine, McMaster University, Hamilton, Ontario, Canada

Requests for reprints: Carole L. Yauk, Environmental Health Centre, Tunney's Pasture, Postal locator 0803A, Ottawa, Ontario, Canada. Phone: 613-941-7376; Fax: 613-941-8530; E-mail: carole_yauk{at}hc-sc.gc.ca.

Despite the presence of known mutagens and carcinogens in cigarette smoke, there is currently no evidence to show that smoking, or exposure to cigarette smoke, can result in heritable genetic mutation. We show that male mice exposed to mainstream tobacco smoke (MTS) exhibit a significant increase in germ-line mutation frequency in spermatogonial stem cells. We exposed mature male mice to MTS for 6 or 12 weeks and investigated mutations arising in exposed spermatogonial stem cells at the expanded simple tandem repeat locus Ms6-hm. A generalized score test showed a significant treatment effect (P = 0.0214). Ms6-hm mutation frequency was 1.4 and 1.7 times higher in mice exposed to MTS for 6 and 12 weeks, respectively, compared with sham controls. The data suggest that mutations accumulate in the spermatogonial stem cells with extended exposures. Mutation spectra were identical between exposed and sham individuals, supporting the hypothesis that tandem repeat mutations arise through indirect mechanisms of mutation. Mutations in sperm that are passed on to offspring cause permanent, irreversible changes in genetic composition and can persist in future generations. Our research suggests that the consequences of smoking extend beyond the smoker to their nonsmoking descendents. [Cancer Res 2007;67(11):5103–4]




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Y. Zhao and R. J. Epstein
Programmed Genetic Instability: A Tumor-Permissive Mechanism for Maintaining the Evolvability of Higher Species through Methylation-Dependent Mutation of DNA Repair Genes in the Male Germ Line
Mol. Biol. Evol., August 1, 2008; 25(8): 1737 - 1749.
[Abstract] [Full Text] [PDF]




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 © 2007 by the American Association for Cancer Research.