Proposed here is a study of the role of total PCBs, individual PCB congeners, DDT and mirex in the etiology of postmenopausal breast cancer. Serum levels of these environmental contaminants will be evaluated. In addition, the association with risk of genetic polymorphisms of enzymes involved in carcinogen metabolism and detoxification (the cytochrome P450 enzymes CYP2D6 and CYP1A1, and glutathione-S-transferase) will be examined. Finally, effect modification of the association of the environmental contaminants with risk by the genetic polymorphisms will be assessed. This study will use stored, frozen (-70 degrees C) blood specimens collected as part of a larger case-control study of diet, reproductive and other factors in risk of postmenopausal breast cancer. Cases (n= 150) have primary, histologically confirmed disease. Population controls (n= 150) will be matched to cases on age and date of blood draw and frequency matched to cases on other breast cancer risk factors other than family history of breast cancer. New blood samples will be drawn for the DNA determinations. Interview data have already been collected on predisease usual diet, medical history, reproductive history and family history of cancer. This study provides an important opportunity for efficient examination of potentially important environmental contaminants in conjunction with evaluation of genetic susceptibility and other known risk factors, in the northeastern U.S., a geographic region at high risk of breast cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project--Cooperative Agreements (U01)
Project #
3U01CA062995-03S1
Application #
2859654
Study Section
Special Emphasis Panel (SRC (94))
Project Start
1993-09-30
Project End
1998-09-29
Budget Start
1995-09-30
Budget End
1998-09-29
Support Year
3
Fiscal Year
1998
Total Cost
Indirect Cost
Name
State University of New York at Buffalo
Department
Public Health & Prev Medicine
Type
Schools of Medicine
DUNS #
038633251
City
Buffalo
State
NY
Country
United States
Zip Code
14260
O'Leary, Erin S; Vena, John E; Freudenheim, Jo L et al. (2004) Pesticide exposure and risk of breast cancer: a nested case-control study of residentially stable women living on Long Island. Environ Res 94:134-44
Freudenheim, Jo L; Bonner, Matthew; Krishnan, Shiva et al. (2004) Diet and alcohol consumption in relation to p53 mutations in breast tumors. Carcinogenesis 25:931-9
Moysich, Kirsten B; Ambrosone, Christine B; Mendola, Pauline et al. (2002) Exposures associated with serum organochlorine levels among postmenopausal women from western New York State. Am J Ind Med 41:102-10
Laden, F; Collman, G; Iwamoto, K et al. (2001) 1,1-Dichloro-2,2-bis(p-chlorophenyl)ethylene and polychlorinated biphenyls and breast cancer: combined analysis of five U.S. studies. J Natl Cancer Inst 93:768-76
Ambrosone, C B; Coles, B F; Freudenheim, J L et al. (1999) Glutathione-S-transferase (GSTM1) genetic polymorphisms do not affect human breast cancer risk, regardless of dietary antioxidants. J Nutr 129:565S-568S
Moysich, K B; Mendola, P; Schisterman, E F et al. (1999) An evaluation of proposed frameworks for grouping polychlorinated biphenyl (PCB) congener data into meaningful analytic units. Am J Ind Med 35:223-31
Freudenheim, J L; Ambrosone, C B; Moysich, K B et al. (1999) Alcohol dehydrogenase 3 genotype modification of the association of alcohol consumption with breast cancer risk. Cancer Causes Control 10:369-77
Ambrosone, C B; Freudenheim, J L; Thompson, P A et al. (1999) Manganese superoxide dismutase (MnSOD) genetic polymorphisms, dietary antioxidants, and risk of breast cancer. Cancer Res 59:602-6
Ambrosone, C B; Freudenheim, J L; Sinha, R et al. (1998) Breast cancer risk, meat consumption and N-acetyltransferase (NAT2) genetic polymorphisms. Int J Cancer 75:825-30
Moysich, K B; Ambrosone, C B; Vena, J E et al. (1998) Environmental organochlorine exposure and postmenopausal breast cancer risk. Cancer Epidemiol Biomarkers Prev 7:181-8

Showing the most recent 10 out of 16 publications