Impact of Polychlorinated Biphenyls Contamination on Estrogenic Activity in Human Male Serum
- 1 October 2005
- journal article
- research article
- Published by Environmental Health Perspectives in Environmental Health Perspectives
- Vol. 113 (10) , 1277-1284
- https://doi.org/10.1289/ehp.7745
Abstract
Polychlorinated biphenyls (PCBs) are thought to cause numerous adverse health effects, but their impact on estrogen signaling is still not fully understood. In the present study, we used the ER-CALUX bioassay to determine estrogenic/antiestrogenic activities of the prevalent PCB congeners and PCB mixtures isolated from human male serum. The samples were collected from residents of an area with an extensive environmental contamination from a former PCB production site as well as from a neighboring background region in eastern Slovakia. We found that the lower-chlorinated PCBs were estrogenic, whereas the prevalent higher-chlorinated PCB congeners 138, 153, 170, 180, 187, 194, 199, and 203, as well as major PCB metabolites, behaved as antiestrogens. Coplanar PCBs had no direct effect on estrogen receptor (ER) activation in this in vitro model. In human male serum samples, high levels of PCBs were associated with a decreased ER-mediated activity and an increased dioxin-like activity, as determined by the DR-CALUX assay. 17 beta-Estradiol (E-2) was responsible for a major part of estrogenic activity identified in total serum extracts. Significant negative correlations were found between dioxin-like activity, as well as mRNA levels of cytochromes P450 1A1 and 1B1 in lymphocytes, and total estrogenic activity. For sample fractions containing only persistent organic pollutants (POPs), the increased frequency of antiestrogenic samples was associated with a higher sum of PCBs. This suggests that the prevalent nondioxin-like PCBs were responsible for the weak antiestrogenic activity of some POPs fractions. Our data also suggest that it might be important to pay attention to direct effects of PCBs on steroid hormone levels in heavily exposed subjects.Keywords
This publication has 57 references indexed in Scilit:
- Toxicity of Hydroxylated and Quinoid PCB Metabolites: Inhibition of Gap Junctional Intercellular Communication and Activation of Aryl Hydrocarbon and Estrogen Receptors in Hepatic and Mammary CellsChemical Research in Toxicology, 2004
- Inhibition of Gap Junctional Intercellular Communication by Noncoplanar Polychlorinated Biphenyls: Inhibitory Potencies and Screening for Potential Mode(s) of ActionToxicological Sciences, 2003
- Effect of chlorinated hydrocarbons on expression of cytochrome P450 1A1, 1A2 and 1B1 and 2- and 4-hydroxylation of 17β-estradiol in female Sprague–Dawley ratsCarcinogenesis: Integrative Cancer Research, 2000
- Comparison of chemical-activated luciferase gene expression bioassay and gas chromatography for PCB determination in human serum and follicular fluid.Environmental Health Perspectives, 2000
- Characterization of potential endocrine-related health effects at low-dose levels of exposure to PCBs.Environmental Health Perspectives, 1999
- 3,3′,4,4′-Tetrachlorobiphenyl exhibits antiestrogenic and antitumorigenic activity in the rodent uterus and mammary cells and in human breast cancer cellsCarcinogenesis: Integrative Cancer Research, 1999
- 3,5,3′,5′-Tetrachlorobiphenyl is a weak oestrogen agonist in vitro and in vivoThe Journal of Steroid Biochemistry and Molecular Biology, 1997
- Effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin, 12-O-tetradecanoylphorbol-13-acetate and 17β-estradiol on estrogen receptor regulation in MCF-7 human breast cancer cellsJournal of Cellular Biochemistry, 1996
- Polychlorinated Biphenyls (PCBs): Environmental Impact, Biochemical and Toxic Responses, and Implications for Risk AssessmentCritical Reviews in Toxicology, 1994
- Polychlorinated biphenyls as inducers of hepatic microsomal enzymes: Structure-activity rulesChemico-Biological Interactions, 1980