The theme of this program project is to develop the scientific bases that are necessary to implement biologically-based risk assessments for several chemicals on the National Priorities List. This will be accomplished by (1) identifying critical mechanisms related to the induction of mutations and cancer by these chemicals, (2) establishing whether or not these mechanisms follow linear or non-linear dose- response relationships between the high doses employed in animal studies and actual or modeled environmental exposures, (4) determining if sensitive populations exist that are not greater or lesser risk to selected chemicals than the general population, (5) developing new methods for determining dermal exposure to hazardous chemicals, (6) investigating factors involved in bioremediation and bioavailability, (7) evaluating mass transfer phenomena in heterogeneous multiphase subsurface systems and enhance methods of remediating such systems, and (8) developing holistochastic human exposure models that integrate space/time distributions of fate and transport with toxicokinetic models linked to human health effects to improve the assessment of risk from hazardous chemicals. The theme addresses many of the stated goals of the Superfund Basic research Program. We will accomplish our task through the investigations proposed in eight research projects and six supporting cores.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Hazardous Substances Basic Research Grants Program (NIEHS) (P42)
Project #
5P42ES005948-13
Application #
6732176
Study Section
Special Emphasis Panel (ZES1-DPB-D (G3))
Program Officer
Thompson, Claudia L
Project Start
1992-04-01
Project End
2006-03-31
Budget Start
2004-04-05
Budget End
2006-03-31
Support Year
13
Fiscal Year
2004
Total Cost
$2,638,339
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Public Health & Prev Medicine
Type
Schools of Public Health
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Luo, Yu-Syuan; Hsieh, Nan-Hung; Soldatow, Valerie Y et al. (2018) Comparative analysis of metabolism of trichloroethylene and tetrachloroethylene among mouse tissues and strains. Toxicology 409:33-43
Balik-Meisner, Michele; Truong, Lisa; Scholl, Elizabeth H et al. (2018) Population genetic diversity in zebrafish lines. Mamm Genome 29:90-100
Luo, Yu-Syuan; Furuya, Shinji; Soldatov, Valerie Y et al. (2018) Metabolism and Toxicity of Trichloroethylene and Tetrachloroethylene in Cytochrome P450 2E1 Knockout and Humanized Transgenic Mice. Toxicol Sci 164:489-500
Balik-Meisner, Michele; Truong, Lisa; Scholl, Elizabeth H et al. (2018) Elucidating Gene-by-Environment Interactions Associated with Differential Susceptibility to Chemical Exposure. Environ Health Perspect 126:067010
To, Kimberly T; Fry, Rebecca C; Reif, David M (2018) Characterizing the effects of missing data and evaluating imputation methods for chemical prioritization applications using ToxPi. BioData Min 11:10
Dalaijamts, Chimeddulam; Cichocki, Joseph A; Luo, Yu-Syuan et al. (2018) Incorporation of the glutathione conjugation pathway in an updated physiologically-based pharmacokinetic model for perchloroethylene in mice. Toxicol Appl Pharmacol 352:142-152
Gray, Kathleen M (2018) From Content Knowledge to Community Change: A Review of Representations of Environmental Health Literacy. Int J Environ Res Public Health 15:
Li, Gen; Jima, Dereje; Wright, Fred A et al. (2018) HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues. BMC Bioinformatics 19:95
Adebambo, Oluwadamilare A; Shea, Damian; Fry, Rebecca C (2018) Cadmium disrupts signaling of the hypoxia-inducible (HIF) and transforming growth factor (TGF-?) pathways in placental JEG-3 trophoblast cells via reactive oxygen species. Toxicol Appl Pharmacol 342:108-115
Smeester, Lisa; Fry, Rebecca C (2018) Long-Term Health Effects and Underlying Biological Mechanisms of Developmental Exposure to Arsenic. Curr Environ Health Rep 5:134-144

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