Risk of breast cancer associated with estrogen DNA adduct biomarker

Kerryn W. Reding, Claire J. Han, Dale Whittington, Muhammad Zahid, Eleanor G. Rogan, Dale Langford, Thomas E. Rohan, Rowan T. Chlebowski, Ting Yuan David Cheng, Wendy E. Barrington, Lesley F. Tinker

Research output: Contribution to journalArticlepeer-review

Abstract

Background: It is biologically plausible that genotoxic estrogens, namely estrogen DNA adducts (EDA), have a role in breast cancer development. Support comes from three prior studies that reported elevated concentrations of EDA relative to estrogen metabolites and conjugates (EDA:EMC) in women with breast cancer relative to control women. Methods: In postmenopausal women in the Women's Health Initiative (WHI), EDA:EMC in 191 controls was compared with findings in 194 prediagnosis urine samples from breast cancer cases. EDA:EMC determinations were by mass spectrometry as previously described, and logistic regression was employed to estimate ORs. Results: EDA:EMC did not differ in breast cancer cases compared with controls overall [0.93 (95% confidence interval, 0.71–1.23)], with a mean (SD) of 2.3 (0.8) and 2.4 (1.1) in cases and controls, respectively. Similarly, the ratio did not differ when examined by estrogen receptor or recency of biospecimen collection prior to breast cancer. Conclusions: Despite the demonstrated genotoxic properties of certain catechol estrogens resulting in EDAs, this analysis did not provide evidence for an increased breast cancer risk in relation to an elevated EDA:EMC. Impact: This analysis, conducted prospectively within postmenopausal women in the WHI study, suggests that a strong association between EDA:EMC and breast cancer could be ruled out, as this study was powered to detect an OR of 2.2 or greater.

Original languageEnglish (US)
Pages (from-to)2096-2099
Number of pages4
JournalCancer Epidemiology Biomarkers and Prevention
Volume29
Issue number10
DOIs
StatePublished - Oct 1 2020

ASJC Scopus subject areas

  • Epidemiology
  • Oncology

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