Cancer Epidemiology
Volume 34, Issue 2 , Pages 142-149, April 2010

Smoking (active and passive), N-acetyltransferase 2, and risk of breast cancer

  • Michael S.C. Conlon

      Affiliations

    • Epidemiology, Outcomes & Evaluation Research, Regional Cancer Program of the Sudbury Regional Hospital, Sudbury, Ontario, Canada P3E 5J1
    • Corresponding Author InformationCorresponding author. Tel.: +1 705 522 6237x2601; fax: +1 705 523 7326.
  • ,
  • Kenneth C. Johnson

      Affiliations

    • Evidence and Risk Assessment Division, Centre for Chronic Disease Prevention and Control, Public Health Agency of Canada, Ottawa, Ontario, Canada K1A 0K9
  • ,
  • Mary A. Bewick

      Affiliations

    • Epidemiology, Outcomes & Evaluation Research, Regional Cancer Program of the Sudbury Regional Hospital, Sudbury, Ontario, Canada P3E 5J1
  • ,
  • Robert M. Lafrenie

      Affiliations

    • Regional Cancer Program of the Sudbury Regional Hospital, Sudbury, Ontario, Canada P3E 5J1
  • ,
  • Allan Donner

      Affiliations

    • Department of Epidemiology and Biostatistics, Schulich School of Medicine and Dentistry, The University of Western Ontario, London, Ontario, Canada N6A 5C1

Accepted 2 February 2010. published online 18 February 2010.

Abstract 

Background: The relationship between smoking and breast cancer remains controversial. The study aim was to assess the relationship of passive and active smoking to breast cancer risk by N-acetyltransferase 2 (NAT2) phenotype, using a comprehensive assessment of both passive and active smoking. Methods: We undertook a population-based case–control study in Northeastern Ontario, Canada of 347 women diagnosed (2002–2004) with breast cancer and 775 population-based controls. The mailed study package included a questionnaire requesting information about established breast cancer risk factors, passive and active smoking, and a buccal swab for genetic analyses. Results: Among never-active smokers, a long duration of passive smoking was associated with an increased risk of breast cancer (odds ratio (OR) 1.86 (95% confidence interval (95% CI) 1.01–3.44) (test for trend (p=0.07)); that risk was more elevated for NAT2 slow acetylators (OR 2.76, 95% CI 1.16–6.59) (and highest in extremely slow acetylators), but not elevated for NAT2 fast acetylators (OR 1.17, 95% CI 0.42–3.23). Among active smokers more than 20 pack-years of smoking was associated with an OR of 1.34 (95% CI 0.92-1.96); more elevated among NAT2 fast acetylators OR 1.93 (95% CI 1.01–3.69) but not elevated among NAT2 slow acetylators. Women who were NAT2 fast acetylators in the highest quartile for duration of active smoking had an OR of 2.74 (95% CI 1.42–5.27), with a significant test of trend (p=0.005). Conclusions: These findings suggest that passive and active smoking may be related to breast cancer, and the effect may be differentially modified by NAT2 phenotype. Further research into the genetic modification of a breast cancer–smoking relationship may help to reconcile earlier discrepant findings.

Keywords: Active smoking, Tobacco smoke pollution, NAT2, Breast neoplasms, Case–control study

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PII: S1877-7821(10)00019-6

doi:10.1016/j.canep.2010.02.001

Cancer Epidemiology
Volume 34, Issue 2 , Pages 142-149, April 2010