Association of CYP1B1 Haplotypes and Breast Cancer Risk in Caucasian Women

  1. Yifan Huang1,
  2. Amy Trentham-Dietz3,4,
  3. Montserrat García-Closas5,
  4. Polly A. Newcomb3,6,
  5. Linda Titus-Ernstoff7,
  6. John M. Hampton4,
  7. Stephen J. Chanock5,
  8. Jonathan L. Haines8 and
  9. Kathleen M. Egan2
  1. 1Biostatistics Core and 2Department of Cancer Prevention and Control, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida; 3Department of Population Health Sciences, University of Wisconsin-Madison and 4University of Wisconsin Paul P. Carbone Comprehensive Cancer Center, Madison, Wisconsin; 5Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland; 6Cancer Prevention Program, Fred Hutchinson Cancer Research Center, Seattle, Washington; 7Dartmouth Medical School, Norris Cotton Cancer Center, Lebanon, New Hampshire; and 8Center for Human Genetics Research, Vanderbilt University School of Medicine, Nashville, Tennessee
  1. Requests for reprints:
    Kathleen Egan, H. Lee Moffitt Cancer Center, 12902 Magnolia Drive, MRC-CANCONT, Tampa, FL 33612. Phone: 813-745-6803; Fax: 813-745-6525. E-mail: Kathleen.Egan{at}Moffitt.org

Abstract

CYP1B1 is a key enzyme involved in estrogen metabolism and may play an important role in the development and progression of breast cancer. In a population-based case-control study, we examined eight CYP1B1 haplotype-tagging single nucleotide polymorphisms in relation to invasive breast cancer risk. Analyses were based on 1,655 cases and 1,470 controls; all women were Caucasian. Among the individual single nucleotide polymorphisms, one (rs9341266) was associated with increased risk of breast cancer (Ptrend = 0.021), although the association was no longer significant after adjusting for multiple tests. A marginally significant haplotype effect was identified (Pglobal = 0.015), with significant associations identified for 2 uncommon haplotypes comprising 4% of the controls. Results suggest that genetic variation in CYP1B1 has at most a minor influence on breast cancer susceptibility among Caucasian women. (Cancer Epidemiol Biomarkers Prev 2009;18(4):1321–3)

Footnotes

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