Firefighting, per‐ and polyfluoroalkyl substances, and DNA methylation of genes associated with prostate cancer risk

Author:

Quaid Margaret1ORCID,Goodrich Jaclyn M.1ORCID,Calkins Miriam M.2,Graber Judith M.3,Urwin Derek45ORCID,Gabriel Jamie4,Caban‐Martinez Alberto J.6,Petroff Rebekah L.1,Grant Casey7,Beitel Shawn C.8,Littau Sally8,Gulotta John J.9,Wallentine Darin9,Hughes Jeff10,Burgess Jefferey L.7

Affiliation:

1. Department of Environmental Health Sciences University of Michigan School of Public Health Ann Arbor Michigan USA

2. National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention Cincinnati Ohio USA

3. Department of Biostatistics and Epidemiology Rutgers the State University of New Jersey Piscataway New Jersey USA

4. Los Angeles County Fire Department Los Angeles California USA

5. Department of Chemistry & Biochemistry UCLA Los Angeles California USA

6. Department of Public Health Sciences University of Miami Miller School of Medicine Miami Florida USA

7. Fire Protection Research Foundation Quincy Massachusetts USA

8. Department of Community, Environment and Policy University of Arizona Mel and Enid Zuckerman College of Public Health Tucson Arizona USA

9. Tucson Fire Department Tucson Arizona USA

10. Orange County Fire Authority Irvine California USA

Abstract

AbstractProstate cancer is the leading incident cancer among men in the United States. Firefighters are diagnosed with this disease at a rate 1.21 times higher than the average population. This increased risk may result from occupational exposures to many toxicants, including per‐ and polyfluoroalkyl substances (PFAS). This study assessed the association between firefighting as an occupation in general or PFAS serum levels, with DNA methylation. Only genomic regions previously linked to prostate cancer risk were selected for analysis: GSTP1, Alu repetitive elements, and the 8q24 chromosomal region. There were 444 male firefighters included in this study, with some analyses being conducted on fewer participants due to missingness. Statistical models were used to test associations between exposures and DNA methylation at CpG sites in the selected genomic regions. Exposure variables included proxies of cumulative firefighting exposures (incumbent versus academy status and years of firefighting experience) and biomarkers of PFAS exposures (serum concentrations of 9 PFAS). Proxies of cumulative exposures were associated with DNA methylation at 15 CpG sites and one region located within FAM83A (q‐value <0.1). SbPFOA was associated with 19 CpG sites (q < 0.1), but due to low detection rates, this PFAS was modeled as detected versus not detected in serum. Overall, there is evidence that firefighting experience is associated with differential DNA methylation in prostate cancer risk loci, but this study did not find evidence that these differences are due to PFAS exposures specifically.

Funder

University of Arizona

Federal Emergency Management Agency

Publisher

Wiley

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