A prospective industrial health surveillance program has been coordinated by Carlo H. Tamburro, M.D., M.P.H., Division of Occupational Toxicology, U. Louisville School of Medicine for the past 20 years. This program provides a unique set of human medical data, work-exposure histories and tissue/serum samples suitable for analysis of short-and long-term biomarkers of toxic chemical exposure. The exposure of this occupational population to industrial chemicals has been continuously monitored and verified for periods of 12-40 years. In the Greater Louisville area, a large medically undeserved and economically-disadvantaged population resides adjacent to the industrial sites and their medical histories can be compared to industrial cohorts. These disadvantage residential populations can be monitored by the proposed biomarker program to assess their body burden relative to the industrial workers and their cohorts. The medical surveillance aspects of this Center will provide essential human medical data, work histories and tissue to develop correlations between the proposed short and long term-biomarkers with the actual disease processes associated with the chemical effluent of these industrial sites. The data obtained would allow more reliable causal linkages to be made or disprove with regard to the populations and validate the biomarkers sensitivity and specificity. The Theme for the U of L Center will focus on the use of biochemical, chemical, and molecular biological biomarkers to define exposure in human populations and to assess in these subjects subsequent health risk requiring preventive and therapeutic modalities. Five Pilot Projects have been selected which would focus on the health surveillance of industrial and residential populations in Louisville exposures to acrylonitrile, vinyl chloride, and a variety of metal catalysts of known toxicological importance. Project 1 (Tamburro/Looney) involves collection, storage, and analysis of medical data & exposure histories and collection of human tissue samples to be analyzed in the biomarker program of the following Projects. Project 2 (Benz/Nerland) will study metabolism of acrylonitrile and vinyl chloride in rat and human hepatocytes. Project 3 (Hurst/Myers) will evaluated biomarkers of intermediate duration of exposure involving hemoglobin and DNA adducts of acrylonitrile. Project 4 (Brennan/Prough) will evaluated short and potentially intermediate-term markers of acrylonitrile, vinyl chloride, and metal catalyst exposure, namely induction and persistence of expression of several enzymes of foreign compound metabolism. Project 5 (Geoghegan/Myers/Wong) will evaluated a long term biomarker, namely mutation of p53 tumor suppressor gene known to be associated with angiosarcomas derived from acrylonitrile exposure in humans.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Exploratory Grants (P20)
Project #
5P20ES006832-02
Application #
2155741
Study Section
Special Emphasis Panel (SRC)
Project Start
1994-04-01
Project End
1997-03-31
Budget Start
1995-04-01
Budget End
1996-03-31
Support Year
2
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Louisville
Department
Biochemistry
Type
Schools of Medicine
DUNS #
City
Louisville
State
KY
Country
United States
Zip Code
40292
Nerland, D E; Cai, J; Pierce Jr, W M et al. (2001) Covalent binding of acrylonitrile to specific rat liver glutathione S-transferases in vivo. Chem Res Toxicol 14:799-806
Mandal, P K; McDaniel, L R; Prough, R A et al. (2001) 7,12-Dimethylbenz[a]anthracene inhibition of steroid production in MA-10 mouse Leydig tumor cells is not directly linked to induction of CYP1B1. Toxicol Appl Pharmacol 175:200-8
Klinge, C M; Kaur, K; Swanson, H I (2000) The aryl hydrocarbon receptor interacts with estrogen receptor alpha and orphan receptors COUP-TFI and ERRalpha1. Arch Biochem Biophys 373:163-74
Klinge, C M (1999) Role of estrogen receptor ligand and estrogen response element sequence on interaction with chicken ovalbumin upstream promoter transcription factor (COUP-TF). J Steroid Biochem Mol Biol 71:1-19
Klinge, C M; Bowers, J L; Kulakosky, P C et al. (1999) The aryl hydrocarbon receptor (AHR)/AHR nuclear translocator (ARNT) heterodimer interacts with naturally occurring estrogen response elements. Mol Cell Endocrinol 157:105-19
Klinge, C M; Studinski-Jones, A L; Kulakosky, P C et al. (1998) Comparison of tamoxifen ligands on estrogen receptor interaction with estrogen response elements. Mol Cell Endocrinol 143:79-90
Klinge, C M; Bodenner, D L; Desai, D et al. (1997) Binding of type II nuclear receptors and estrogen receptor to full and half-site estrogen response elements in vitro. Nucleic Acids Res 25:1903-12
Sathya, G; Li, W; Klinge, C M et al. (1997) Effects of multiple estrogen responsive elements, their spacing, and location on estrogen response of reporter genes. Mol Endocrinol 11:1994-2003
Benz, F W; Nerland, D E; Li, J et al. (1997) Dose dependence of covalent binding of acrylonitrile to tissue protein and globin in rats. Fundam Appl Toxicol 36:149-56
Clark, B J; Combs, R; Hales, K H et al. (1997) Inhibition of transcription affects synthesis of steroidogenic acute regulatory protein and steroidogenesis in MA-10 mouse Leydig tumor cells. Endocrinology 138:4893-901

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