Sanchez Hugo, Hossain Mohammad B, Lera Lydia, Hirsch Sandra, Albala Cecilia, Uauy Ricardo, Broberg Karin, Ronco Ana M
Unidad de Nutrición Pública, Instituto de Nutrición y Tecnología de los Alimentos Doctor. Fernando Monckeberg Barros (INTA), Universidad de Chile, El Líbano 5524, Macul, Santiago, Chile.
Division of Occupational and Environmental Medicine, Lund University, Lund, Sweden.
Clin Epigenetics. 2017 Jul 24;9:74. doi: 10.1186/s13148-017-0374-y. eCollection 2017.
Changes in DNA methylation, one of the most studied epigenetic mechanisms, are considered an initial marker for early cancer detection. We evaluated how availability of dietary factors (folates and vitamin B12) involved in one-carbon metabolism may contribute to DNA methylation changes of cancer-related genes in human subjects.
We studied, by pyrosequencing, the methylation of tumor suppressor gene , DNA repair genes and , and the repetitive element LINE-1 (as a surrogate for global DNA methylation), in blood of elderly individuals ( = 249) who had been exposed to folic acid (FA) through FA-fortified wheat flour during the last 12 years.
We found that serum folate and to a lesser extent, vitamin B12 concentrations, were significantly correlated with DNA methylation of , , and , but not with . High serum folate concentrations (>45.3 nmol/L) were present in 31.1% of the participants. Although the methylated fraction of CpG sites in , , and was low (1.17-3.8%), high folate concentrations were significantly associated with methylation at the 3rd tertile of specific CpG sites in all genes with OR between 1.97 and 4.17.
This study shows that a public policy, like food fortification with FA that increases circulating serum folate levels, could affect methylation levels of specific genes linked to cancer risk. Our present results deserve additional studies to clarify the real impact of high FA levels for risk of cancer in a whole population chronically exposed to a fortified food such as wheat flour.
ISRCTN 48153354 and ISRCTN 02694183.
DNA甲基化是研究最多的表观遗传机制之一,其变化被认为是早期癌症检测的初始标志物。我们评估了参与一碳代谢的膳食因素(叶酸和维生素B12)的可利用性如何影响人类受试者癌症相关基因的DNA甲基化变化。
我们通过焦磷酸测序研究了老年个体(n = 249)血液中肿瘤抑制基因、DNA修复基因和的甲基化情况,以及重复元件LINE-1(作为整体DNA甲基化的替代指标),这些个体在过去12年中通过强化叶酸的小麦粉接触了叶酸(FA)。
我们发现血清叶酸以及在较小程度上维生素B12的浓度与、和的DNA甲基化显著相关,但与无关。31.1%的参与者血清叶酸浓度较高(>45.3 nmol/L)。尽管、和中CpG位点的甲基化比例较低(1.17 - 3.8%),但高叶酸浓度与所有基因中特定CpG位点第三个三分位数处的甲基化显著相关,OR值在1.97至4.17之间。
本研究表明,像用叶酸强化食品这样的公共政策会提高循环血清叶酸水平,可能会影响与癌症风险相关的特定基因的甲基化水平。我们目前的结果值得进一步研究,以阐明高叶酸水平对长期接触强化食品如小麦粉的整个人群患癌风险的实际影响。
ISRCTN 48153354和ISRCTN 02694183。