AMACR Polymorphisms, Dietary Intake of Red Meat and Dairy and Prostate Cancer Risk

被引:20
作者
Wright, Jonathan L. [1 ,2 ]
Neuhouser, Marian L. [2 ]
Lin, Daniel W. [2 ]
Kwon, Erika M. [3 ]
Feng, Ziding [2 ]
Ostrander, Elaine A. [3 ]
Stanford, Janet L. [2 ,4 ]
机构
[1] Univ Washington, Med Ctr, Dept Urol, Sch Med, Seattle, WA 98195 USA
[2] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA
[3] NHGRI, Canc Genet Branch, Bethesda, MD 20892 USA
[4] Univ Washington, Sch Publ Hlth, Dept Epidemiol, Seattle, WA 98195 USA
关键词
prostate cancer; AMACR; red meat; dairy; SNP; METHYLACYL-COA RACEMASE; CELLS IN-VITRO; SEQUENCE VARIANTS; PHYTANIC ACID; ALPHA; PRODUCTS; POPULATION; RECEPTOR; EXPRESSION; CONVERSION;
D O I
10.1002/pros.21267
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND. Alpha-methylacyl CoA racemase (AMACR) is an enzyme involved in fatty acids metabolism. One of AMACRs primary substrates, phytanic acid, is principally obtained from dietary red meat/dairy, which are associated with prostate cancer (PCa) risk. AMACR is also a tumor tissue biomarker over-expressed in PCa. In this study, we explored the potential relationship between AMACR polymorphisms, red meat/dairy intake, and PCa risk. METHODS. Caucasian participants from two population-based PCa case-control studies were included. AMACR single nucleotide polymorphisms (SNPs) were selected to capture variation across the gene and regulatory regions. Red meat and dairy intake was determined from food frequency questionnaires. The odds ratio (OR) of PCa (overall and by disease aggressiveness) was estimated by logistic and polytomous regression. Potential interactions between genotypes and dietary exposures were evaluated. RESULTS. Data from 1,309 cases and 1,267 controls were analyzed. Carriers of the variant T allele (rs2287939) had an OR of 0.81 (95% CI 0.68-0.97) for less aggressive PCa, but no alteration in risk for more aggressive PCa. Red meat consumption was positively associated with PCa risk, and the association was stronger for more aggressive disease (lowest vs. highest tertile OR = 1.55, 95% CI 1.10-2.20). No effect modification of AMACR polymorphisms by either dietary red meat or dairy intake on PCa risk was observed. CONCLUSIONS. PCa risk varied by level of red meat intake and by one AMACR SNP, but there was no evidence for gene-environment interaction. These findings suggest that the effects of AMACR polymorphisms and red meat and dairy on PCa risk are independent. Prostate 71: 498-506, 2011. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:498 / 506
页数:9
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