Associations between Catalase Phenotype and Genotype: Modification by Epidemiologic Factors
- Jiyoung Ahn1,6,
- Susan Nowell3,
- Susan E. McCann1,
- Jihnhee Yu2,
- Lisa Carter1,
- Nicholas P. Lang3,4,
- Fred F. Kadlubar5,
- Luke D. Ratnasinghe5 and
- Christine B. Ambrosone1
- 1Department of Epidemiology, Roswell Park Cancer Institute; 2Department of Biostatistics, State University of New York at Buffalo, Buffalo, New York; 3University of Arkansas for Medical Sciences; 4Central Arkansas Veterans Healthcare System, Little Rock, Arkansas; 5Division of Pharmacogenomics and Molecular Epidemiology, National Center for Toxicological Research, Jefferson, Arkansas; and 6Nutritional Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NZH, Bethesda, Maryland
- Requests for reprints:
Christine Ambrosone, Department of Epidemiology, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263. Phone: 716-845-3082; Fax: 716-845-8125. E-mail: christine.ambrosone{at}roswellpark.org
Abstract
Catalase is an endogenous antioxidant enzyme that neutralizes hydrogen peroxide and is induced by oxidative challenge. A −262C → T polymorphism in the promoter region of the gene (CAT) is associated with risk of several conditions related to oxidative stress. We sought to determine the functional effects of the CAT polymorphism on enzyme activity in erythrocytes and the potential modifying effects of demographic and lifestyle factors on genotype/phenotype relationships, using specimens and data from controls from breast and prostate cancer studies in Arkansas (n = 420). There was a dose-response reduction in catalase activity by genotype, with geometric means of 115.4 units/mg hemoglobin for those with CC genotypes, 82.1 units/mg for those with CT genotypes, and 73.5 units/mg for those with TT genotypes. Associations were only observed among Caucasians (P < 0.0001), with no effects among African Americans (P = 0.91), and were stronger among women than men, although numbers in stratified analyses were small. Differences in catalase activity by genotype were most pronounced among those in the highest tertiles of consumption of fruits and vegetables (−35%, P = 0.003), with weaker relationships among those who were lower consumers (−21.8%, P = 0.16). Among those with CC genotypes, there was no change in activity by consumption, but there were notable decreases in activity by tertiles of consumption for those with at least one T allele. These data indicate that the CAT −262C → T polymorphism predicts a portion of catalase phenotype, which may be limited to Caucasians. Associations between genotype and phenotype were modified by dietary factors, illustrating the biochemical complexity of studies of genetic polymorphisms and disease risk. (Cancer Epidemiol Biomarkers Prev 2006;15(6):1217-22)
Footnotes
-
Grant support: NCI grants R01 CA095222 and R01 AG15722-03 and DAMD17-98-I-A800.
-
The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
-
- Accepted April 26, 2006.
- Received February 7, 2006.
- Revision received March 28, 2006.










