Cox David G, Tamimi Rulla M, Hunter David J
Program in Molecular and Genetic Epidemiology, Epidemiology Department, Harvard School of Public Health, 677 Huntington Ave., Boston, MA 02115, USA.
BMC Cancer. 2006 Aug 31;6:217. doi: 10.1186/1471-2407-6-217.
Germ-line mutations in genes such as BRCA1, BRCA2, and ATM can cause a substantial increase in risk of breast cancer. However, these mutations are rare in the general population, and account for little of the incidence of sporadic breast cancer in the general population. Therefore, research has been focused on examining associations between common polymorphisms and breast cancer risk. To date, few associations have been described. This has led to the hypothesis that breast cancer is a complex disease, whereby a constellation of very low penetrance alleles need to be carried to present a risk phenotype. Polymorphisms in the manganese superoxide dismutase (MnSOD) and glutathione peroxidase (GPX-1) genes have been proposed as low penetrance alleles, and have not been clearly associated with breast cancer. We investigated whether variants at both polymorphisms, while not independently associated with breast cancer risk, could influence breast cancer risk when considered together.
A case-control study nested within the Nurses' Health Study was performed comparing 1262 women diagnosed with breast cancer to 1533 disease free women. The MnSOD (Val16Ala, rs1799725) and GPX-1 (Pro198Leu, rs1050450) were genotyped via TaqMan assay. Disease risk was evaluated using logistic regression.
While neither allele alone shows any change in breast cancer risk, an increase in the risk of breast cancer (OR 1.87, 95% CI 1.09 - 3.19) is observed in individuals who carry both the Ala16Ala genotype of MnSOD and the Leu198Leu genotype of GPX-1.
Polymorphisms in the GPX-1 and MnSOD genes are associated with an increased risk of breast cancer.
BRCA1、BRCA2和ATM等基因的种系突变可导致乳腺癌风险大幅增加。然而,这些突变在普通人群中很少见,在普通人群散发性乳腺癌的发病率中所占比例很小。因此,研究一直集中在检查常见多态性与乳腺癌风险之间的关联。迄今为止,鲜有此类关联被描述。这导致了一种假说,即乳腺癌是一种复杂疾病,需要携带一系列低外显率等位基因才会呈现出风险表型。锰超氧化物歧化酶(MnSOD)和谷胱甘肽过氧化物酶(GPX-1)基因的多态性已被认为是低外显率等位基因,但尚未明确与乳腺癌相关。我们研究了这两种多态性的变体虽然各自与乳腺癌风险无独立关联,但共同考虑时是否会影响乳腺癌风险。
在护士健康研究中进行了一项病例对照研究,将1262例诊断为乳腺癌的女性与1533例无病女性进行比较。通过TaqMan分析对MnSOD(Val16Ala,rs1799725)和GPX-1(Pro198Leu,rs1050450)进行基因分型。使用逻辑回归评估疾病风险。
虽然单独的任何一个等位基因都未显示出乳腺癌风险有任何变化,但同时携带MnSOD的Ala16Ala基因型和GPX-1的Leu198Leu基因型的个体中,观察到乳腺癌风险增加(比值比1.87,95%可信区间1.09 - 3.19)。
GPX-1和MnSOD基因的多态性与乳腺癌风险增加相关。