Program - Society of Toxicology
Program - Society of Toxicology
Program - Society of Toxicology
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44 th Annual Meeting<br />
and ToxExpo<br />
<strong>Program</strong> Description<br />
#327 1:30 ENVIRONMENTAL TERRORISM:<br />
DEVELOPMENT OF EVACUATION, RE-ENTRY<br />
AND RE-USE GUIDELINES FOR CHEMICAL,<br />
BIOLOGICAL AND RADIOLOGICAL AGENTS.<br />
M. A. Maddaloni. U.S. EPA, New York. Sponsor: A.<br />
Jarabek.<br />
#328 1:45 AN EPA PERSPECTIVE ON CHEMICAL<br />
CONTAMINATION CLEAN-UP. S. Sterling, I. P.<br />
Baumel and C. Sonich-Mullin. ORD/NHSRC, U.S.<br />
EPA, Washington, DC. Sponsor: M. Maddaloni.<br />
#329 2:15 A MILITARY APPROACH TO ASSESSING<br />
HEALTH RISK. V. Hauschild and B. Thran.<br />
Directorate <strong>of</strong> Health Risk Management, US Army Ctr<br />
for Health Promotion and Preventive Medicine,<br />
Aberdeen Proving Ground, Edgewood Area, MD.<br />
Sponsor: M. Maddaloni.<br />
#330 2:45 BIOTERRORIST THREATS TO THE US FOOD<br />
SUPPLY SYSTEM: A RISK ASSESSMENT<br />
PERSPECTIVE. B. Hope. Air Quality Division,<br />
Oregon Department <strong>of</strong> Environmental Quality, Portland,<br />
OR. Sponsor: A. Jarabeck.<br />
#331 3:15 A PRIMER ON RADIATION ISSUES RELATED<br />
TO NUCLEAR TERRORISM. S. L. Simon.<br />
Radiation Epidemiology Branch, National Cancer<br />
Institutes, Bethesda, MD. Sponsor: M. Maddaloni.<br />
#332 3:45 DEVELOPMENT OF OPERATIONAL<br />
GUIDELINES FOR CONSEQUENCE<br />
MANAGEMENT OF RADIOLOGICAL<br />
DISPERSAL DEVICE INCIDENTS. S. Domotor 1 , A.<br />
Wallo 1 , C. YU 2 , D. LePoire 2 and S. Kamboj 2 . 1 US<br />
DOE, Washington, DC and 2 Argonne National<br />
Laboratory, Washington, DC. Sponsor: A. Jarabek.<br />
Monday Afternoon, March 7<br />
1:30 PM to 4:30 PM<br />
Room RO6<br />
WORKSHOP SESSION: HIGH THROUGHPUT SCREENING<br />
APPROACHES IN GENETIC TOXICOLOGY<br />
Chairperson(s): Jiri Aubrecht, Pfizer, Inc., Groton, CT and Robert Schiestl,<br />
University <strong>of</strong> California, Los Angeles, Los Angeles, CA.<br />
Endorsed by:<br />
In Vitro SS*<br />
Risk Assessment SS<br />
Recent progress in combinatorial chemistry, molecular biology, genomics, and<br />
automation has enabled identifying a relatively large number <strong>of</strong> compounds<br />
capable <strong>of</strong> reacting with intended pharmacological targets. However, 40% <strong>of</strong><br />
drug candidates ultimately fail during clinical development due to safety related<br />
issues. The overall attrition <strong>of</strong> drug candidates due to genetic toxicology issues<br />
alone includes about 12% <strong>of</strong> drug candidates. This causes delays in the introduction<br />
<strong>of</strong> vital drugs to patients and significant economic losses. Therefore, the<br />
development <strong>of</strong> relevant mechanism-based high throughput screening technologies<br />
to assess genetic toxicity at the early stages <strong>of</strong> drug discovery with<br />
relatively limited amount <strong>of</strong> chemical is extremely important. Genetic toxicology<br />
provides the necessary information for assessment <strong>of</strong> the genotoxic risk<br />
associated with the use <strong>of</strong> drugs. Since the beginning <strong>of</strong> genotoxicity testing in<br />
the early 1970s, many different test systems have been developed and used.<br />
Since no single test is capable <strong>of</strong> detecting all genotoxic agents, the current standard<br />
in vitro genotoxicity testing consists <strong>of</strong> evaluating mutagenicity (bacterial<br />
reverse mutation assay) and chromosome damage (lymphocyte aberration assay<br />
or mouse lymphoma assay). Unfortunately, these standard in vitro assays are not<br />
amenable to high throughput testing and their application in early phases <strong>of</strong> drug<br />
discovery is not feasible. Therefore, the research and assay development efforts<br />
have been directed to developing alternative approaches, technologies and/or<br />
endpoints. The speakers in this session present emerging state-<strong>of</strong>-the-art technologies<br />
under development and/or currently used in the pharmaceutical<br />
industry. The topics covered in this symposium comprise high throughput<br />
versions <strong>of</strong> the Salmonella assay, assays for DNA deletions, chromosome aberrations,<br />
the comet assay and a gene expression reporter assay. The presentations<br />
will cover exciting developments that may spark further interest in the automation<br />
<strong>of</strong> genotoxicity assays.<br />
#333 1:30 HIGH THROUGHPUT SCREENING<br />
APPROACHES IN GENETIC TOXICOLOGY. R.<br />
H. Schiestl 2 and J. Aubrecht 1 . 1 Safety Sciences, Pfizer,<br />
Inc., Groton, CT and 2 Departments <strong>of</strong> Pathology and<br />
Environmental Health, UCLA, Los Angeles, CA.<br />
#334 1:40 BIOLUMINESCENT SALMONELLA REVERSE<br />
MUTATION ASSAY: A HIGH THROUGHPUT<br />
APPROACH FOR DETECTION OF<br />
MUTAGENICITY. J. Aubrecht. Safety Sciences,<br />
Pfizer, Inc., Groton, CT.<br />
#335 2:10 BIOLUMINESCENT YEAST DEL ASSAY TO<br />
DETECT CARCINOGENS AND CLASTOGENS. R.<br />
Schiestl 1 and J. Aubrecht 2 . 1 Pathology, UCLA, Los<br />
Angeles, CA and 2 Safety Sciences, Pfizer, Inc., Groton,<br />
CT.<br />
#336 2:40 APPLICATION OF A HIGH THROUGHPUT<br />
COMET ASSAY IN DRUG DISCOVERY. A.<br />
Hartmann 1 and W. Frieauff 2 . 1 Non Clinical Safety,<br />
F.H<strong>of</strong>fmann-La Roche Ltd., Basel, Switzerland and<br />
2 GenSafe / Precinical Safety, Novartis Pharmacology,<br />
Basel, Switzerland. Sponsor: J. Aubrecht.<br />
MONDAY<br />
up-to-date information at www.toxicology.org 73