Molecular Genetics Laboratory, Department of Pathology and Forensic Medicine, School of Medicine, Federal University of Ceará, Coronel Nunes de Melo, 1315, Rodolfo Teófilo, Fortaleza, CE, CEP 60430-270, Brazil.
Mol Biol Rep. 2012 Apr;39(4):4899-907. doi: 10.1007/s11033-011-1285-1. Epub 2011 Dec 2.
Polymorphisms in genes involved in folate metabolism have been shown to be implicated in breast cancer risk but with contradictory results. In this case-control study, we investigated the association between MTHFR C677T and A1298C, TYMS 5'-UTR, MTR A2756G and cSHMT C1420T and also the folate carrier (RFC1 G80A) and breast cancer risk in a northeastern Brazilian population. The study included 183 women diagnosed with breast cancer and 183 controls volunteers without any history of cancer. Also a significant number of healthy individuals were included for allelic frequency in the population studied. Risk of breast cancer was estimated by conditional logistic regression. An association with risk was found for women carrying the MTR A2756G polymorphic allele (AG, P = 0.0036; AG/GG, P = 0.0040), and a protective effect in carriers of the RFC1 G80A polymorphic allele (GA, P = 0.0015; AA, P = 0.0042). Stratifying the data by age (cutoff point of 50 years old), different distributions were observed for breast cancer risk. For women ≤50 years, the risk observed in the presence of the polymorphic allele MTR 2756 (AG/GG) in the general analysis was, restricted to this age group (P = 0.0118). Conversely, for women over 50, the risk of breast cancer development was statistically associated with the MTHFR 677CT genotype, but especially significant was risk associated with the presence of the polymorphic allele of cSHMT C1420T (P = 0.0120) and the protective effect associated with the RFC1 G80A polymorphism allele (P = 0.0021), was restrict to this age group. These data indicate that the cutoff age used (50 years old) was appropriate, since it was able to discriminate risk in each age group in the population studied and also to point to the importance of age in the analyses of cancer-associated polymorphisms.
参与叶酸代谢的基因多态性已被证明与乳腺癌风险有关,但结果却相互矛盾。在这项病例对照研究中,我们调查了 MTHFR C677T 和 A1298C、TYMS 5'-UTR、MTR A2756G 和 cSHMT C1420T 以及叶酸载体(RFC1 G80A)与巴西东北部人群乳腺癌风险之间的关联。该研究纳入了 183 名被诊断患有乳腺癌的女性和 183 名无癌症病史的对照组志愿者。此外,还纳入了大量健康个体以确定研究人群中的等位基因频率。通过条件逻辑回归估计乳腺癌风险。携带 MTR A2756G 多态性等位基因(AG,P=0.0036;AG/GG,P=0.0040)的女性患乳腺癌的风险与风险相关,而携带 RFC1 G80A 多态性等位基因(GA,P=0.0015;AA,P=0.0042)的女性则具有保护作用。按年龄(50 岁为临界点)对数据进行分层,观察到不同的乳腺癌风险分布。对于≤50 岁的女性,在一般分析中,MTR 2756 多态性(AG/GG)存在时观察到的风险,仅限于该年龄组(P=0.0118)。相反,对于 50 岁以上的女性,乳腺癌发病风险与 MTHFR 677CT 基因型呈统计学相关,尤其是与 cSHMT C1420T 多态性等位基因(P=0.0120)相关的风险和与 RFC1 G80A 多态性等位基因(P=0.0021)相关的保护作用,仅限于该年龄组。这些数据表明,使用的截止年龄(50 岁)是合适的,因为它能够区分研究人群中每个年龄组的风险,并指出年龄在癌症相关多态性分析中的重要性。