© 2000 by Oxford University Press
Journal of the National Cancer Institute, Vol. 92, No. 22, 1831-1836,
November 15, 2000
© 2000 Oxford University Press
REPORT |
Associations Between Cigarette Smoking, Lifestyle Factors, and Microsatellite Instability in Colon Tumors
Affiliations of authors: M. L. Slattery, K. Curtin, K.-N. Ma, S. Edwards (Health Research Center, Department of Family and Preventive Medicine), L. Ballard, M. Leppert (Department of Human Genetics), W. S. Samowitz (Department of Surgical Pathology), University of Utah, Salt Lake City; K. Anderson, University of Minnesota, School of Public Health, Minneapolis; D. Schaffer, Division of Research, Kaiser Permanente Medical Care Program, Oakland, CA; J. Potter, Fred Hutchinson Cancer Research Center, Seattle, WA.
Correspondence to: Martha L. Slattery, Ph.D., M.P.H., Health Research Center, Department of Family and Preventive Medicine, University of Utah, 391 Chipeta Way, Suite G, Salt Lake City, UT 84108 (e-mail: mslatter{at}dfpm.utah.edu).
Background: Microsatellite instability (MSI) has been reported to occur in approximately 10%15% of colon tumors. MSI is characterized by the presence of mutations in tandemly repeated DNA sequences known as microsatellites. Some individuals with unstable tumors have inherited mutations in mismatch repair genes, but MSI is also observed in sporadic colon cancer. It is unknown whether lifestyle factors associated with colon cancer, such as physical activity, body size, cigarette smoking, or use of aspirin and/or nonsteroidal anti-inflammatory drugs, contribute to MSI in sporadic tumors. Methods: Data from a population-based, casecontrol study of colon cancer were used. Case subjects were between 30 and 79 years of age at the time of diagnosis and included both men and women. Questionnaire data were used to obtain information on lifestyle factors. Tumor MSI was determined with the use of a panel of 10 tetranucleotide repeats and two mononucleotide repeats. A total of 1510 case subjects had valid questionnaire data and tumor DNA from which we were able to obtain MSI status. Questionnaire data were compared with lifestyle factors reported by 2410 population-based control subjects. All statistical tests were two-sided. Results: MSI-positive (MSI+) tumors were most common in older people and women and in the proximal colon. Patients with MSI+ tumors were more likely to smoke 20 or more cigarettes a day than case subjects with MSI-negative (MSI-) tumors (odds ratio for being a smoker = 1.6 [95% confidence interval = 1.02.5] for men and 2.2 [95% confidence interval = 1.43.5] for women). The association between MSI+ tumors and cigarette smoking was strongest among case subjects who started to smoke at a young age, smoked for 35 or more years, and were either current smokers or had stopped fewer than 15 years before diagnosis. A statistically significant linear trend of increased risk of MSI+ tumors was observed with increasing amount smoked (P<.01). Conclusions: This study suggests that smoking cigarettes statistically significantly contributes to MSI in colon tumors. We estimate that approximately 21% of MSI in colon tumors may be attributable to cigarette smoking.
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