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Program - Society of Toxicology

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<strong>Society</strong> <strong>of</strong> <strong>Toxicology</strong> 2011<br />

<strong>Program</strong> Description (Continued)<br />

Abstract #<br />

Monday Afternoon, March 7<br />

2:00 PM to 4:45 PM<br />

Room 207<br />

Environment and Disease<br />

Symposium Session: Human Variability in Susceptibility to<br />

Environmental Toxicants<br />

Chairperson(s): Holly Mortensen, U.S. EPA, Durham, NC, and<br />

Susan Euling, U.S. EPA, Washington, D.C.<br />

Sponsor:<br />

Molecular Biology Specialty Section<br />

Endorsed by:<br />

Regulatory and Safety Evaluation Specialty Section<br />

Risk Assessment Specialty Section<br />

Defining the differing levels <strong>of</strong> susceptibility across human populations<br />

in response to environmental chemicals can provide information to define<br />

population risk factors and in turn, allow for risk levels to be based on the<br />

most susceptible populations. Data from high-throughput/high content (HT/<br />

HC) technologies, including 'omics, have been integral in the identification<br />

and characterization <strong>of</strong> drug-target or disease loci and have the potential<br />

to be informative for characterizing the effects and dose-response assessment<br />

<strong>of</strong> chemical exposure and outcomes within genetically heterogeneous<br />

populations. Many <strong>of</strong> the same 'omics technologies have been successfully<br />

utilized to provide data that informs the mechanism <strong>of</strong> action for<br />

environmental chemicals, including the identification <strong>of</strong> perturbed toxicity<br />

pathways. In addition, large scale population genotyping studies, such as the<br />

HapMap, can help to establish levels <strong>of</strong> variability at chemical-associated,<br />

target loci across human populations, and in comparison to genome-wide<br />

patterns. Individual genotype-phenotype combinations can then be verified<br />

using in vitro methods, or extrapolation from animal models. This session<br />

includes talks on some <strong>of</strong> the latest approaches to informing population<br />

variability and the identification <strong>of</strong> susceptible populations through the use<br />

<strong>of</strong> HT/HC data, particularly from genomics technologies. We will discuss<br />

how 'omics data in combination with data from enhanced animal models,<br />

publically available datasets and related computational tools can be used<br />

to identify biomarkers, and subsequently define risk for genetically heterogeneous<br />

populations, and how this variability translates to human risk and<br />

progression <strong>of</strong> disease.<br />

#819 2:00 HUMAN VARIABILITY IN SUSCEPTIBILITY<br />

TO ENVIRONMENTAL TOXICANTS. ​H.<br />

Mortensen. NCCT, U.S. EPA, Research Triangle<br />

Park, NC.<br />

2:00 INTRODUCTION. ​Holly Mortensen<br />

#820 2:05 POPULATION-BASED DISCOVERY OF<br />

TOXICOGENOMICS BIOMARKERS FOR<br />

HEPATOTOXICITY. ​I. Rusyn. Environmental<br />

Sciences and Engineering, University <strong>of</strong> North<br />

Carolina at Chapel Hill, Chapel Hill, NC.<br />

#821 2:37 EXPERIMENTALLY DEFINING TOXICITY<br />

PATHWAYS USING IN VITRO HIGH-<br />

CONTENT SCREENING OF EMBRYONIC<br />

FIBROBLASTS FROM THE MOUSE<br />

DIVERSITY PANEL. ​R. Thomas. Genomic<br />

Biology and Bioinformatics, The Hamner Institutes<br />

for Health Sciences, Research Triangle Park, NC.<br />

#822 3:09 HERITABILITY IN DOSE RESPONSE -<br />

PUTTING THE HORSE BEFORE THE CART. ​<br />

A. Motsinger-Reif. Department <strong>of</strong> Statistics, North<br />

Carolina State University, Raleigh, NC. Sponsor: H.<br />

Mortensen.<br />

Abstract #<br />

#823 3:41 ASSOCIATION OF GENETIC<br />

POLYMORPHISMS, MRNA EXPRESSION<br />

OF P53 AND P21 WITH CHRONIC<br />

BENZENE POISONING IN A CHINESE<br />

OCCUPATIONAL POPULATION. ​N. Rothman.<br />

Division <strong>of</strong> Cancer Epidemiology and Genetics,<br />

National Cancer Institute, Bethesda, MD. Sponsor:<br />

H. Mortensen.<br />

#824 4:13 PERSONALIZED MEDICINE,<br />

INDIVIDUALIZED DRUG THERAPY:<br />

CAN THESE GOALS BE REALISTICALLY<br />

ACHIEVED? ​D. W. Nebert. Departments <strong>of</strong><br />

Environmental Health & Pediatrics, Division <strong>of</strong><br />

Human Genetics, University Cincinnati Medical<br />

Center, Cincinnati, OH.<br />

Monday Afternoon, March 7<br />

2:00 PM to 4:45 PM<br />

Room 204<br />

Symposium Session: Toxicological Considerations in the Gulf<br />

<strong>of</strong> Mexico Oil Spill<br />

Chairperson(s): Michael Madden, U.S. EPA, Chapel Hill, NC, and<br />

Michael Ottlinger, U.S. EPA, Cincinnati, OH.<br />

Sponsor:<br />

Occupational Public Health Specialty Section<br />

The Deepwater Horizon oil rig explosion on April 20, 2010 resulted in a<br />

release <strong>of</strong> petroleum crude oil into Gulf <strong>of</strong> Mexico waters. The release,<br />

41 miles <strong>of</strong>fshore, was about 1 mile in Department Oil dispersants were<br />

employed to change surface oil and underwater properties. Surface oil was<br />

also combusted and physical barriers deployed. Oil was estimated to have<br />

spread to an estimated 2500 square mile in the Gulf. On July 15, the well<br />

head was capped reducing oil flow to a minimum. A number <strong>of</strong> exposure<br />

uncertainties have arisen as a result <strong>of</strong> the spill related to the locations<br />

the oil has dispersed to, including volatilization to the atmosphere; and<br />

the dose <strong>of</strong> contaminant reaching wildlife, humans, and vegetation in the<br />

affected areas, and physicochemical properties <strong>of</strong> the dispersant-treated<br />

and aged oil. We will present findings related to understanding the migration<br />

<strong>of</strong> the spill components, the habitats and organisms contaminated, and<br />

the characteristics <strong>of</strong> altered crude. Routes <strong>of</strong> exposure for humans to oil<br />

components will be presented in part based on data from other studied oil<br />

spills. Knowledge <strong>of</strong> these currently unsure parameters will assist in understanding<br />

the potential biological and health effects induced by the spill. The<br />

major possible ecological effects will be described and compared to the<br />

normal Gulf ecosystem dynamics. The choice <strong>of</strong> the specific oil dispersants<br />

utilized will be discussed with an emphasis on the toxicity assays employed;<br />

toxicity endpoints still not fully examined will be identified. The types and<br />

likelihood <strong>of</strong> possible human adverse health effects, both acute and latent,<br />

will be presented in light <strong>of</strong> what will be known <strong>of</strong> the exposure routes<br />

and the conditions (e.g. heat). In order to comprehend possible effects in a<br />

comprehensive manner in order to develop estimates <strong>of</strong> various risks, the<br />

data sources available to perform such an assessment will be identified (e.g.,<br />

estimates <strong>of</strong> contaminated seafood consumption). Finally, data deficiencies<br />

needed for risk assessment will be described.<br />

#825 2:00 TOXICOLOGICAL CONSIDERATIONS IN<br />

THE GULF OF MEXICO OIL SPILL. ​M. C.<br />

Madden. ORD, NHEERL, HSD, Clinical Research<br />

Branch, U.S. EPA, Chapel Hill, NC.<br />

#826 2:00 THE GULF OF MEXICO ECOSYSTEM:<br />

CONSEQUENCES OF THE BP OIL SPILL. ​W.<br />

Benson, S. Jordan, R. Greene, V. Engle, M. Hemmer<br />

and M. Barron. Gulf Ecology Division, U.S. EPA,<br />

Gulf Breeze, FL.<br />

MONday<br />

Poster Sessions<br />

Regional Interest Session<br />

Roundtable Sessions<br />

Symposium Sessions<br />

Thematic Sessions<br />

Workshop Sessions<br />

185

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