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首页> 外文期刊>Epigenetics: official journal of the DNA Methylation Society >The influence of one-carbon metabolism on gene promoter methylation in a population-based breast cancer study
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The influence of one-carbon metabolism on gene promoter methylation in a population-based breast cancer study

机译:在基于人群的乳腺癌研究中,一碳代谢对基因启动子甲基化的影响

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Abnormal methylation in gene promoters is a hallmark of the cancer genome; however, factors that may influence promoter methylation have not been well elucidated. As the one-carbon metabolism pathway provides the universal methyl donor for methylation reactions, perturbation of this pathway might influence DNA methylation and, ultimately, affect gene functions. Utilizing approximately 800 breast cancer tumor tissues from a large population-based study, we investigated the relationships between dietary and genetic factors involved in the one-carbon metabolism pathway and promoter methylation of a panel of 13 breast cancer-related genes. We found that CCND2, HIN1 and CHD1 were the most "dietary sensitive" genes, as methylation of their promoters was associated with intakes of at least two out of the eight dietary methyl factors examined. On the other hand, some micronutrients (i.e., B 2 and B 6) were more "epigenetically active" as their intake levels correlated with promoter methylation status in 3 out of the 13 breast cancer genes evaluated. Both positive (hypermethylation) and inverse (hypomethylation) associations with high micronutrient intake were observed. Unlike what we saw for dietary factors, we did not observe any clear patterns between one-carbon genetic polymorphisms and the promoter methylation status of the genes examined. Our results provide preliminary evidence that one-carbon metabolism may have the capacity to influence the breast cancer epigenome. Given that epigenetic alterations are thought to occur early in cancer development and are potentially reversible, dietary modifications may offer promising venues for cancer intervention and prevention.
机译:基因启动子中的甲基化异常是癌症基因组的标志。然而,尚未充分阐明可能影响启动子甲基化的因素。由于一碳代谢途径为甲基化反应提供了通用的甲基供体,因此该途径的干扰可能会影响DNA甲基化,并最终影响基因功能。利用来自一项基于人口的大型研究的大约800个乳腺癌肿瘤组织,我们调查了涉及13个与乳腺癌相关的基因的一碳代谢途径与启动子甲基化的饮食和遗传因素之间的关系。我们发现CCND2,HIN1和CHD1是最“饮食敏感”的基因,因为其启动子的甲基化与所研究的八个饮食甲基因子中至少两个的摄取有关。另一方面,某些微量营养素(即B 2和B 6)在摄入的水平与所评估的13个乳腺癌基因中的3个基因中的3个与启动子甲基化状态相关,因此更具“表观遗传活性”。观察到高微量营养素摄入的正(高甲基化)和反向(低甲基化)关联。与我们在饮食因素上看到的不同,我们没有观察到一碳遗传多态性与所检查基因的启动子甲基化状态之间的任何清晰模式。我们的结果提供了初步证据,表明一碳代谢可能具有影响乳腺癌表观基因组的能力。鉴于表观遗传学改变被认为发生在癌症发展的早期,并且可能是可逆的,饮食结构的改变可能为癌症的干预和预防提供有希望的场所。

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