Polymorphisms in estrogen biosynthesis and metabolism-related genes, ionizing radiation exposure, and risk of breast cancer among US radiologic technologists

Alice J. Sigurdson, Parveen Bhatti, Shih Chen Chang, Preetha Rajaraman, Michele M. Doody, Laura Bowen, Steven L. Simon, Robert M. Weinstock, Martha S. Linet, Marvin Rosenstein, Marilyn Stovall, Bruce H. Alexander, Dale L. Preston, Jeffery P. Struewing

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

Ionizing radiation-associated breast cancer risk appears to be modified by timing of reproductive events such as age at radiation exposure, parity, age at first live birth, and age at menopause. However, potential breast cancer risk modification of low to moderate radiation dose by polymorphic estrogen metabolism-related gene variants has not been routinely investigated. We assessed breast cancer risk of 12 candidate variants in 12 genes involved in steroid metabolism, catabolism, binding, or receptor functions in a study of 859 cases and 1,083 controls within the US radiologic technologists (USRT) cohort. Using cumulative breast dose estimates from a detailed assessment of occupational and personal diagnostic ionizing radiation exposure, we investigated the joint effects of genotype on the risk of breast cancer. In multivariate analyses, we observed a significantly decreased risk of breast cancer associated with the CYP3A4 M445T minor allele (rs4986910, OR = 0.3; 95% CI 0.1-0.9). We found a borderline increased breast cancer risk with having both minor alleles of CYP1B1 V432L (rs1056836, CC vs. GG, OR = 1.2; 95% CI 0.9-1.6). Assuming a recessive model, the minor allele of CYP1B1 V432L significantly increased the dose-response relationship between personal diagnostic X-ray exposure and breast cancer risk, adjusted for cumulative occupational radiation dose (p interaction = 0.03) and had a similar joint effect for cumulative occupational radiation dose adjusted for personal diagnostic X-ray exposure (p interaction = 0.06). We found suggestive evidence that common variants in selected estrogen metabolizing genes may modify the association between ionizing radiation exposure and breast cancer risk.

Original languageEnglish (US)
Pages (from-to)177-184
Number of pages8
JournalBreast Cancer Research and Treatment
Volume118
Issue number1
DOIs
StatePublished - Nov 2009

Bibliographical note

Funding Information:
Acknowledgments We are grateful to the radiologic technologists who participated in the USRT study; Jerry Reid of the American Registry of Radiologic Technologists for continued support of this study; and Diane Kampa and Allison Iwan of the University of Minnesota for data collection and study coordination. This study was supported by the Intramural Research Program of the Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health.

Keywords

  • Casecontrol
  • Estrogen biosynthesis
  • Interaction
  • Ionizing radiation
  • Polymorphisms
  • Radiologic technologists
  • Risk factors

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