The common 677C>T gene polymorphism of methylenetetrahydrofolate reductase gene is not associated with breast cancer risk

被引:52
作者
Langsenlehner, U
Krippl, P
Renner, W
Yazdani-Biuki, B
Wolf, G
Wascher, TC
Paulweber, B
Weitzer, W
Samonigg, H
机构
[1] Landeskrankenanstalten Salzburg, Dept Internal Med, Salzburg, Austria
[2] Karl Franzens Univ Graz, Div Nucl Med, Dept Radiol, Graz, Austria
[3] Karl Franzens Univ Graz, Dept Internal Med, Graz, Austria
[4] Karl Franzens Univ Graz, Clin Inst Med & Lab Diagnost, Graz, Austria
[5] Karl Franzens Univ Graz, Div Oncol, Dept Internal Med, Graz, Austria
关键词
breast cancer; epidemiology; genetics; methylenetetrahydrofolate reductase; MTHFR 677C > T polymorphism;
D O I
10.1023/A:1025752420309
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Methylenetetrahydrofolate reductase (MTHFR) is involved in folate metabolism and plays a role in DNA biosynthesis, methylation, and repair in actively dividing cells. A common 677C>T polymorphism in the gene for MTHFR, leading to a thermolabile enzyme with decreased activity, has been associated with reduced plasma folate levels and elevated homocysteine levels and could be a risk factor for breast cancer. In the present case-control study, MTHFR genotype was determined in 500 women with clinically verified breast cancer and 500 female age-matched healthy control subjects. The homozygous TT genotype was found in 13.0% patients and 13.1% controls (P = n.s.). The odds ratio of TT homozygotes for breast cancer was 0.99 (95% confidence interval 0.68-1.43). The MTHFR genotype was furthermore not associated with tumor size, histological grading, estrogen or progesterone receptor status and age at diagnosis. In a subgroup of 116 premenopausal patients, no increased frequency of the homozygous 677T genotype was found (13.8%). Therefore, we conclude that the MTHFR 677C>T polymorphism is not associated with individual susceptibility to breast cancer.
引用
收藏
页码:169 / 172
页数:4
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