Environmental contaminants that mimic the effects of estrogen have been suggested to contribute to the high incidence of breast cancer in Western populations. In both in vitro and in vivo experiments, cadmium has been shown to possess potent estrogen-like activity, including proliferation of breast cancer cells, activation and increased expression of estrogen regulated genes, and activation of the estrogen receptor-1. Further, cadmium is classified as a known human carcinogen by the International Agency for Research on Cancer. This combination of estrogenic and carcinogenic activity makes cadmium a contaminant of particularly high concern for breast cancer. One modest-sized epidemiologic study suggests risk at cadmium exposure levels common to the upper quartile of the general population implying that cadmium may play a substantial role in breast cancer;however this study used urine cadmium collected after diagnosis. As a result, it has been questioned whether increased cadmium is a risk factor for breast cancer, or whether it reflects the effects of treatment or disease. In light of mechanistic and preliminary epidemiologic evidence supporting a cadmium-breast cancer relationship, this project aims to rigorously investigate the association between urinary cadmium levels collected prediagnostically and risk of breast cancer in a case-cohort study population from the Danish Diet Cancer and Health (DCH) prospective cohort. This is one of the few, if not only, cohorts in the world with adequate power for investigating breast cancer along with urine samples collected pre-diagnostically and available on all participants. Among the 57,053 members of the DCH cohort we will identify 900 cases of female breast cancer, and randomly select 900 women as a comparison group (sub-cohort) according to the efficient case-cohort design. Female population will be limited to those postmenopausal at baseline because most breast cancer cases occur in postmenopausal women. Urine samples will be analyzed for cadmium, other metals, and creatinine. This study will provide reliable and valuable insight into the hypothesized association between cadmium exposure in a general population and breast cancer and will assess whether zinc intake and smoking history modify these relationships. Analyses will also be stratified by ductal and lobular histology, in situ / invasive status, estrogen receptor positive, stage of cancer, along with other variables to investigate sensitivity of results and effect modification. The proposed study will address pressing questions posed by recent results and will overcome several methodological limitations of previous studies related to precision of the exposure assessment, study size, and possible bias in previous retrospective designs. If the study shows an association between urinary cadmium level and risk of breast cancer, there is great potential for prevention with more extensive regulation to avoid population exposure, since primary sources of general population exposure to cadmium are well recognized.

Public Health Relevance

Breast cancer accounts for 200,000 new cases and 40,000 deaths in the United States each year;few modifiable risk factors have been identified. Mechanistic and early epidemiologic evidence suggest that cadmium, a known lung carcinogen, mimics endocrine hormones and may contribute to the high incidence rates of breast cancer in Western industrialized nations. This study seeks to shed light on whether urinary cadmium, a biomarker of decades-long exposure, is associated with breast cancer using a case-cohort epidemiologic study design and the Danish Diet and Cancer Cohort, one of the few cohorts in the world with adequate power for investigating cancer outcomes along with urine samples collected pre-diagnostically and available on all participants.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES019209-03
Application #
8415525
Study Section
Epidemiology of Cancer Study Section (EPIC)
Program Officer
Dilworth, Caroline H
Project Start
2011-04-01
Project End
2015-01-31
Budget Start
2013-02-01
Budget End
2014-01-31
Support Year
3
Fiscal Year
2013
Total Cost
$267,196
Indirect Cost
$33,800
Name
State University New York Stony Brook
Department
Public Health & Prev Medicine
Type
Schools of Medicine
DUNS #
804878247
City
Stony Brook
State
NY
Country
United States
Zip Code
11794
Roswall, Nina; Hvidtfeldt, Ulla A; Harrington, James et al. (2018) Predictors of Urinary Arsenic Levels among Postmenopausal Danish Women. Int J Environ Res Public Health 15:
Monastero, Rebecca N; Vacchi-Suzzi, Caterina; Marsit, Carmen et al. (2018) Expression of Genes Involved in Stress, Toxicity, Inflammation, and Autoimmunity in Relation to Cadmium, Mercury, and Lead in Human Blood: A Pilot Study. Toxics 6:
Vacchi-Suzzi, Caterina; Viens, Laura; Harrington, James M et al. (2018) Low levels of lead and glutathione markers of redox status in human blood. Environ Geochem Health 40:1175-1185
Vacchi-Suzzi, Caterina; Porucznik, Christina A; Cox, Kyley J et al. (2017) Temporal variability of urinary cadmium in spot urine samples and first morning voids. J Expo Sci Environ Epidemiol 27:306-312
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Karimi, Roxanne; Vacchi-Suzzi, Caterina; Meliker, Jaymie R (2016) Mercury exposure and a shift toward oxidative stress in avid seafood consumers. Environ Res 146:100-7
Vacchi-Suzzi, Caterina; Karimi, Roxanne; Kruse, Danielle et al. (2016) Low-level mercury, omega-3 index and neurobehavioral outcomes in an adult US coastal population. Eur J Nutr 55:699-711
Vacchi-Suzzi, Caterina; Kruse, Danielle; Harrington, James et al. (2016) Is Urinary Cadmium a Biomarker of Long-term Exposure in Humans? A Review. Curr Environ Health Rep 3:450-458
Vacchi-Suzzi, Caterina; Eriksen, Kirsten T; Levine, Keith et al. (2015) Dietary Intake Estimates and Urinary Cadmium Levels in Danish Postmenopausal Women. PLoS One 10:e0138784
Eriksen, Kirsten T; Halkjær, Jytte; Meliker, Jaymie R et al. (2015) Dietary cadmium intake and risk of prostate cancer: a Danish prospective cohort study. BMC Cancer 15:177

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