The overall research goal of the Environmental Carcinogenesis Program (ECP) is to provide insight into the mechanisms by which environmental agents cause disease. By investigating selected model chemicals of risk to rodents and humans, it may be possible to improve out understanding of the mechanisms of mutagenesis and carcinogenesis in model rodent systems. This could lead to predicting the relative risk to human health for environmental chemical exposure and to be able to identify or predict affects of chemicals that possess similar properties. Thus, the overall goal is to understand and apply knowledge gained in this endeavor to the prevention of human disease. To achieve these goals, it is the Program's mission to develop and validate methods to assess the affects of chemicals on oncogenes, suppressor genes, and other critical molecular determinants in neoplastic processes and to develop and validate methods to rapidly assess the toxicologic and carcinogenic potential of mutagenic and nonmutagenic chemicals. To fulfill this mission, this contract shall provide the opportunity to investigate transgenic models for use in carcinogenic, mutagenic, as well as molelcular studies. In addition, it shall allow for the more efficient evaluation of transgenic strains in order to determine which if any of the strains would be most useful for further indepth studies and to provide an understanding of the mechanisms involved in the neoplastic process.

Project Start
1996-05-07
Project End
2001-04-30
Budget Start
1997-09-25
Budget End
1998-07-31
Support Year
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Integrated Laboratory Systems, Inc.
Department
Type
DUNS #
City
Research Triangle Park
State
NC
Country
United States
Zip Code
27709
Bennett, L M; McAllister, K A; Malphurs, J et al. (2000) Mice heterozygous for a Brca1 or Brca2 mutation display distinct mammary gland and ovarian phenotypes in response to diethylstilbestrol. Cancer Res 60:3461-9
Tennant, R W; Stasiewicz, S; Mennear, J et al. (1999) Genetically altered mouse models for identifying carcinogens. IARC Sci Publ :123-50