Associations between catalase phenotype and genotype: Modification by epidemiologic factors

被引:93
作者
Ahn, Jiyoung
Nowell, Susan
McCann, Susan E.
Yu, Jihnhee
Carter, Lisa
Lang, Nicholas P.
Kadlubar, Fred F.
Ratnasinghe, Luke D.
Ambrosone, Christine B.
机构
[1] Roswell Pk Canc Inst, Dept Epidemiol, Buffalo, NY 14263 USA
[2] SUNY Buffalo, Dept Biostat, New York, NY USA
[3] Univ Arkansas Med Sci, Little Rock, AR 72205 USA
[4] Cent Arkansas Vet Healthcare Syst, Little Rock, AR 72205 USA
[5] Natl Ctr Toxicol Res, Div Pharmacogenom & Mol Epidemiol, Jefferson, AR 72079 USA
[6] NCI, Nutr Epidemiol Branch, Div Canc Epidemiol & Genet, NZH, Bethesda, MD USA
关键词
D O I
10.1158/1055-9965.EPI-06-0104
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
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.
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页码:1217 / 1222
页数:6
相关论文
共 20 条
[1]
Associations between breast cancer risk and the catalase genotype, fruit and vegetable consumption, and supplement use [J].
Ahn, J ;
Gammon, MD ;
Santella, RM ;
Gaudet, MM ;
Britton, JA ;
Teitelbaum, SL ;
Terry, MB ;
Nowell, S ;
Davis, W ;
Garza, C ;
Neugut, AI ;
Ambrosone, CB .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2005, 162 (10) :943-952
[2]
Ahn J, 2006, OXIDATIVE STRESS, DISEASE AND CANCER, P897, DOI 10.1142/9781860948046_0032
[3]
Susceptibility to arsenic-induced hyperkeratosis and oxidative stress genes myeloperoxidase and catalase [J].
Ahsan, H ;
Chen, Y ;
Kibriya, MG ;
Islam, MN ;
Slavkovich, VN ;
Graziano, JH ;
Santella, RM .
CANCER LETTERS, 2003, 201 (01) :57-65
[4]
Oxidants and Antioxidants in Breast Cancer [J].
Ambrosone, Christine B. .
ANTIOXIDANTS & REDOX SIGNALING, 2000, 2 (04) :903-918
[5]
Oxidative nucleobase modifications leading to strand scission [J].
Burrows, CJ ;
Muller, JG .
CHEMICAL REVIEWS, 1998, 98 (03) :1109-1151
[6]
Genetic association of the Catalase gene (CAT) with vitiligo susceptibility [J].
Casp, CB ;
She, JX ;
McCormack, WT .
PIGMENT CELL RESEARCH, 2002, 15 (01) :62-66
[7]
OXYGEN RADICALS AND HUMAN-DISEASE [J].
CROSS, CE ;
HALLIWELL, B ;
BORISH, ET ;
PRYOR, WA ;
AMES, BN ;
SAUL, RL ;
MCCORD, JM ;
HARMAN, D .
ANNALS OF INTERNAL MEDICINE, 1987, 107 (04) :526-545
[8]
Dietrich M, 2002, CANCER EPIDEM BIOMAR, V11, P7
[9]
FEIG DI, 1994, CANCER RES, V54, pS1890
[10]
A common functional C-T substitution polymorphism in the promoter region of the human catalase gene influences transcription factor binding, reporter gene transcription and is correlated to blood catalase levels [J].
Forsberg, L ;
Lyrenäs, L ;
de Faire, U ;
Morgenstern, R .
FREE RADICAL BIOLOGY AND MEDICINE, 2001, 30 (05) :500-505