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Grantee Research Project Results

Species-Specific Endocrine Disruption: PCB- and PAH-Induced Estrogenic Effects

EPA Grant Number: R826301
Title: Species-Specific Endocrine Disruption: PCB- and PAH-Induced Estrogenic Effects
Investigators: Zacharewski, Timothy
Institution: Michigan State University
EPA Project Officer: Aja, Hayley
Project Period: January 1, 1998 through December 31, 2000
Project Amount: $282,998
RFA: Endocrine Disruptors (1997) RFA Text |  Recipients Lists
Research Category: Environmental Justice , Endocrine Disruptors , Human Health , Safer Chemicals

Description:

Accumulating evidence suggests that chemicals and complex mixtures are capable of eliciting endocrine disrupting activities that adversely affect human and wildlife health, and jeopardize environmental quality. Several studies have shown numerous species are experiencing compromised reproductive fitness and there has also been significant increases in the incidence of hormone-dependent cancers. It has been proposed that some of these effects may be due to exposure to chemicals and/or complex mixtures that possess estrogen receptor-mediated activities. These substances are commonly referred to as environmental estrogens.

Estrogens and the estrogen receptor (ER) play major roles in a number of physiological processes such as the regulation of developmental processes, homeostasis and fertility as well as in pathological conditions such as hormone-dependent diseases. Although the function and activities of estrogen and the ER are conserved between species, the amino acid sequence of the ligand binding domains of the ERs are less conserved. This suggests that species may exhibit different responses and sensitivities to non-traditional estrogenic ligands and that one species may not be an appropriate surrogate to identify and to assess the risks environmental estrogens pose to human and wildlife health. The intent of this proposal is to examine the estrogenic activities of polychlorinated biphenyls (PCBs) and polyaromatic hydrocarbons (PAHs) and to examine their effects in a number of species including rodents, birds, fish and amphibians.

Rodent, avian, aquatic and amphibian species exhibit different sensitivities to environmental estrogens due to different ligand preferences and binding affinities to the estrogen receptor.

Approach:

An integrative approach will be used that involves a battery of in vitro and in vivo assays. Species specific differences in ligand preference and binding affinities initially identified using in vitro assays (i.e. receptor binding, gene expression) will subsequently be verified in vivo by monitoring gene expression (e.g. vitellogenin).

Publications and Presentations:

Publications have been submitted on this project: View all 50 publications for this project

Journal Articles:

Journal Articles have been submitted on this project: View all 10 journal articles for this project

Supplemental Keywords:

toxicology, cancer, sperm, mechanisms, pollutants, pesticides, industrial chemicals, steroids, rats, mice, fish, birds, frogs., RFA, Health, Scientific Discipline, Toxics, Waste, Environmental Chemistry, Health Risk Assessment, Endocrine Disruptors - Environmental Exposure & Risk, HAPS, endocrine disruptors, chemical mixtures, Risk Assessments, Biochemistry, Children's Health, Endocrine Disruptors - Human Health, adverse outcomes, complex mixtures, endocrine disrupting chemicals, PCBs, fertility, industrial chemicals, PAH, animal models, carcinogens, human growth and development, cancer, human exposure, estrogen response, reproductive processes, estrogen receptors, biological effects

Relevant Websites:

http://www.bch.msu.edu/~zacharet/ Exit

Progress and Final Reports:

  • 1998
  • 1999 Progress Report
  • Final Report
  • Top of Page

    The perspectives, information and conclusions conveyed in research project abstracts, progress reports, final reports, journal abstracts and journal publications convey the viewpoints of the principal investigator and may not represent the views and policies of ORD and EPA. Conclusions drawn by the principal investigators have not been reviewed by the Agency.

    Project Research Results

    • Final Report
    • 1999 Progress Report
    • 1998
    50 publications for this project
    10 journal articles for this project

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