Genetic variations in genes involved in the metabolic activation and/or detoxification of tobacco carcinogens are likely to be a major source of inter-individual and inter-racial variation in cancer susceptibility. These metabolic differences are often associated with genetic polymorphisms in genes coding for carcinogen metabolizing enzymes. Therefore, the carcinogenic capacity of tobacco and tobacco smoke may be dependent upon the genetic composition of enzymes responsible for metabolizing of these carcinogens, thereby affecting individual susceptibility to tobacco- related cancers. One of the important enzymes involved in the metabolism of major tobacco-smoke carcinogens including | polycyclic aromatic hydrocarbons like benzo[a]pyrene (BaP) is epoxide hydrolase (EH). The EH enzyme catalyzes the conversion of BaP-(7,8)-epoxide to BaP-(7,8)-diol, which is the direct precursor metabolite of BaP-(7,8)-diol-(9,10)-epoxide, the ultimate carcinogen of BaP. Previous studies have implicated EH polymorphisms in increased risk for lung as well as oral cancer in Caucasian cohorts but have not included an | assessment of EH polymorphisms and cancer risk in other racial groups. We have established the presence of other EH gene polymorphisms that could potentially play a role in EH activity. As EH plays a key role in the activation of PAHs, a full exploration of EH genetic variants must be performed and the role of polymorphic EH alleles on EH activity. Our hypothesis is that newly-identified EH genetic polymorphisms play an important role in affecting enzyme activity. The goal of the present study is to elucidate novel and examine known or newly-identified polymorphisms present in the EH gene. In this proposal, we intend to examine the prevalence of newly identified as well as known polymorphisms in Caucasians as well as African Americans. In addition, we will examine the potential role of these polymorphisms in EH activity by functional analysis of each allele. These studies will provide baseline information for future large-scale case:control studies regarding the potential of these polymorphisms to affect cancer risk and influence our strategies in terms of cancer prevention for smoking-related cancers.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Small Research Grants (R03)
Project #
5R03CA091314-02
Application #
6515084
Study Section
Subcommittee G - Education (NCI)
Program Officer
Verma, Mukesh
Project Start
2001-06-01
Project End
2004-05-31
Budget Start
2002-06-18
Budget End
2004-05-31
Support Year
2
Fiscal Year
2002
Total Cost
$72,500
Indirect Cost
Name
University of South Florida
Department
Pathology
Type
Schools of Medicine
DUNS #
City
Tampa
State
FL
Country
United States
Zip Code
33612
Park, Jong Y; Chen, Lan; Lee, JiHyun et al. (2005) Polymorphisms in the promoter region of neutrophil elastase gene and lung cancer risk. Lung Cancer 48:315-21
Park, Jong Y; Chen, Lan; Wadhwa, Nina et al. (2005) Polymorphisms for microsomal epoxide hydrolase and genetic susceptibility to COPD. Int J Mol Med 15:443-8
Park, J Y; Chen, L; Elahi, A et al. (2005) Genetic analysis of microsomal epoxide hydrolase gene and its association with lung cancer risk. Eur J Cancer Prev 14:223-30
Park, Jong Y; Schantz, Stimson P; Lazarus, Philip (2003) Epoxide hydrolase genotype and orolaryngeal cancer risk: interaction with GSTM1 genotype. Oral Oncol 39:483-90