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Association of Estrogen Metabolism with Breast Cancer Risk in Different Cohorts of Postmenopausal Women.
Sampson, Joshua N; Falk, Roni T; Schairer, Catherine; Moore, Steven C; Fuhrman, Barbara J; Dallal, Cher M; Bauer, Douglas C; Dorgan, Joanne F; Shu, Xiao-Ou; Zheng, Wei; Brinton, Louise A; Gail, Mitchell H; Ziegler, Regina G; Xu, Xia; Hoover, Robert N; Gierach, Gretchen L.
Affiliation
  • Sampson JN; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland. gierachg@mail.nih.gov sampsonjn@mail.nih.gov.
  • Falk RT; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
  • Schairer C; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
  • Moore SC; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
  • Fuhrman BJ; University of Arkansas for Medical Sciences, Fay W. Boozman College of Public Health, Little Rock, Arkansas.
  • Dallal CM; University of Maryland School of Public Health, College Park, Maryland.
  • Bauer DC; University of California at San Francisco, San Francisco, California.
  • Dorgan JF; University of Maryland School of Medicine, Baltimore, Maryland.
  • Shu XO; Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, Tennessee.
  • Zheng W; Vanderbilt-Ingram Cancer Center, Vanderbilt University School of Medicine, Nashville, Tennessee.
  • Brinton LA; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
  • Gail MH; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
  • Ziegler RG; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
  • Xu X; Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Frederick, Maryland.
  • Hoover RN; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland.
  • Gierach GL; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland. gierachg@mail.nih.gov sampsonjn@mail.nih.gov.
Cancer Res ; 77(4): 918-925, 2017 02 15.
Article in En | MEDLINE | ID: mdl-28011624
Endogenous estradiol and estrone are linked causally to increased risks of breast cancer. In this study, we evaluated multiple competing hypotheses for how metabolism of these parent estrogens may influence risk. Prediagnostic concentrations of estradiol, estrone, and 13 metabolites were measured in 1,298 postmenopausal cases of breast cancer and 1,524 matched controls in four separate patient cohorts. The median time between sample collection and diagnosis was 4.4 to 12.7 years across the cohorts. Estrogen analytes were measured in serum or urine by liquid chromatography-tandem mass spectrometry. Total estrogen levels (summing all 15 estrogens/estrogen metabolites) were associated strongly and positively with breast cancer risk. Normalizing total estrogen levels, we also found that a relative increase in levels of 2-hydroxylation pathway metabolites, or in the ratio of 2-hydroxylation:16-hydroxylation pathway metabolites, were associated inversely with breast cancer risk. These associations varied by total estrogen levels, with the largest risk reductions occurring in women in the highest tertile. With appropriate validation, these findings suggest opportunities for breast cancer prevention by modifying individual estrogen metabolism profiles through either lifestyle alterations or chemopreventive strategies. Cancer Res; 77(4); 918-25. ©2017 AACR.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Estrogens Type of study: Etiology_studies / Incidence_studies / Observational_studies Limits: Adult / Aged / Female / Humans / Middle aged Language: En Journal: Cancer Res Year: 2017 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Estrogens Type of study: Etiology_studies / Incidence_studies / Observational_studies Limits: Adult / Aged / Female / Humans / Middle aged Language: En Journal: Cancer Res Year: 2017 Document type: Article Country of publication: United States