Naushad Shaik Mohammad, Divya Chandrasekhar, Janaki Ramaiah M, Hussain Tajamul, Alrokayan Salman A, Kutala Vijay Kumar
Biochemical Genetics, Sandor Life Sciences Pvt Ltd, Banjara Hills, Road No. 3, Hyderabad, 500034, India.
School of Chemical and Biotechnology, SASTRA University, Tirumalaisamudram, Thanjavur, 613401, India.
J Community Genet. 2016 Oct;7(4):279-290. doi: 10.1007/s12687-016-0277-1. Epub 2016 Aug 19.
Aberrations in one-carbon metabolism were reported to increase breast cancer risk by influencing the DNA synthesis and methylation of DNA and catecholamines. However, the results of these association studies remain inconclusive. We have explored the contribution of eight genetic polymorphisms in modulating the susceptibility to breast cancer by performing a meta-analysis of worldwide studies. In total, 62 case-control studies representing 17 different populations involving 18,117 breast cancer cases and 23,573 healthy controls were included in this meta-analysis. Out of the eight polymorphisms analyzed, methylenetetrahydrofolate reductase (MTHFR) C677T exhibited positive association with the breast cancer risk in both fixed effects (OR 1.14, 95 % CI 1.10-1.17) and random effects (OR 1.10, 95 % CI 1.02-1.18) models. Solute carrier family 19 (folate transporter), member 1 (SLC19A1) G80A exhibited positive association (OR 1.16, 95 % CI 1.03-1.31) while MTR A2756G exhibited an inverse association (OR 0.78, 95 % CI 0.75-0.82) with the breast in fixed effect model alone. Significant heterogeneity was observed in the association of MTHFR C677T with breast cancer even between studies from the same geographical area, specifically among Chinese, Indians, and Turks. Subgroup analysis revealed MTHFR C677T-mediated breast cancer risk in post-menopausal women and women with low dietary intake of folate. Geographical area wise segregation of data revealed MTHFR-mediated increased breast cancer risk in populations who consume methionine-rich diet. Altitude-level variations were observed in the association of SHMT1 C1420T with breast cancer. India and Brazil of same altitude showed an inverse association with this polymorphism, while USA and China that share similar altitude showed a null association. MTHFR C677T and SLC19A1 G80A are the two polymorphisms of one-carbon metabolic pathway that increase breast cancer in the worldwide population. Dietary patterns and altitudinal variations are the likely risk modulators that are contributing toward ethnic- and population-level variations in genetic associations.
据报道,一碳代谢异常通过影响DNA合成、DNA甲基化和儿茶酚胺增加乳腺癌风险。然而,这些关联研究的结果仍无定论。我们通过对全球研究进行荟萃分析,探讨了8种基因多态性在调节乳腺癌易感性中的作用。本荟萃分析共纳入了62项病例对照研究,代表17个不同人群,涉及18117例乳腺癌病例和23573例健康对照。在分析的8种多态性中,亚甲基四氢叶酸还原酶(MTHFR)C677T在固定效应模型(OR 1.14,95%CI 1.10 - 1.17)和随机效应模型(OR 1.10,95%CI 1.02 - 1.18)中均与乳腺癌风险呈正相关。溶质载体家族19(叶酸转运体)成员1(SLC19A1)G80A呈正相关(OR 1.16,95%CI 1.03 - 1.31),而MTR A2756G仅在固定效应模型中与乳腺癌呈负相关(OR 0.78,95%CI 0.75 - 0.82)。即使在来自同一地理区域的研究之间,特别是在中国、印度和土耳其的研究中,也观察到MTHFR C677T与乳腺癌的关联存在显著异质性。亚组分析揭示了MTHFR C677T介导的绝经后妇女和叶酸饮食摄入量低的妇女患乳腺癌的风险。按地理区域对数据进行分类显示,在食用富含蛋氨酸饮食的人群中,MTHFR介导的乳腺癌风险增加。观察到丝氨酸羟甲基转移酶1(SHMT1)C1420T与乳腺癌的关联存在海拔水平差异。印度和巴西海拔相同,该多态性与之呈负相关,而美国和中国海拔相似,与之无关联。MTHFR C677T和SLC19A1 G80A是一碳代谢途径中的两种多态性,它们在全球人群中增加乳腺癌风险。饮食模式和海拔差异可能是导致基因关联在种族和人群水平上存在差异的风险调节因素。