Institute of Health Research INCLIVA, Valencia, Spain.
PLoS One. 2013;8(1):e53902. doi: 10.1371/journal.pone.0053902. Epub 2013 Jan 16.
Lifetime exposure to estrogen is a factor that plays an important role in the pathogenesis and progression of breast cancer. Genetic variants in genes of the biosynthesis and metabolism of estrogen have been associated with breast cancer risk. Among them, the CYP19 gene encodes for aromatase, the enzyme that catalyzes the conversion of androgens to estrogens. The rs10046 polymorphism on the CYP19 gene has been related to levels of circulating estradiol and to the estradiol/testosterone ratio. To date, epidemiological studies of rs10046 have been performed in different populations with contradictory results. In the present study, we have conducted a case-control analysis (522 cases and 1221 controls) in a Spanish population. Furthermore, we have performed a meta-analysis including 20,098 subjects (7,998 cases and 12,100 controls) to summarize the data available for rs10046 and breast cancer risk. An odds ratio (OR) with a 95% confidence interval (CI) was applied to assess the association. The results of our case-control study show an association between the carriers of at least one C allele (dominant model) and breast cancer risk (OR = 1.29, 95% CI 1.01-1.66, p-value = 0.038). The meta-analysis shows no significant association with breast cancer risk in any of the genetic models tested. The analysis by ethnic subgroups also failed to produce associations. The evaluation of heterogeneity, influence analysis, and publication bias confirms the reliability of the analysis. We can conclude that the rs10046 polymorphism on CYP19 by itself does not constitute breast cancer risk. We cannot, however, reject the possibility that it could contribute (interact), together with other genetic variants, to modify the circulating levels of estradiol.
一生中暴露于雌激素是乳腺癌发病和进展的一个重要因素。雌激素生物合成和代谢基因中的遗传变异与乳腺癌风险相关。其中,CYP19 基因编码芳香酶,该酶催化雄激素转化为雌激素。CYP19 基因上的 rs10046 多态性与循环雌二醇水平和雌二醇/睾酮比值有关。迄今为止,rs10046 的流行病学研究在不同人群中进行,结果相互矛盾。在本研究中,我们在西班牙人群中进行了病例对照分析(522 例病例和 1221 例对照)。此外,我们进行了荟萃分析,纳入了 20098 名受试者(7998 例病例和 12100 例对照),以总结 rs10046 与乳腺癌风险的数据。应用比值比(OR)和 95%置信区间(CI)评估相关性。我们的病例对照研究结果表明,至少携带一个 C 等位基因的携带者(显性模型)与乳腺癌风险相关(OR=1.29,95%CI 1.01-1.66,p 值=0.038)。荟萃分析显示,在测试的任何遗传模型中,rs10046 与乳腺癌风险均无显著相关性。亚组分析也未能产生相关性。异质性评估、影响分析和发表偏倚证实了分析的可靠性。我们可以得出结论,CYP19 上的 rs10046 多态性本身不能构成乳腺癌风险。然而,我们不能排除它与其他遗传变异一起(相互作用),从而改变雌二醇的循环水平,从而导致乳腺癌风险增加的可能性。