首页> 外文期刊>The British Journal of Nutrition >Methylation status of CpG islands in the promoter region of genes differentially expressed in colonic mucosa from adenoma patients and controls in response to altered vegetable intake
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Methylation status of CpG islands in the promoter region of genes differentially expressed in colonic mucosa from adenoma patients and controls in response to altered vegetable intake

机译:CpG岛甲基化状态的基因启动子区域在腺瘤患者结肠黏膜中差异表达的基因以及对照对蔬菜摄入量变化的响应

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摘要

Vegetables may protect against colorectal cancer (CRC) via changes in gene expression involved in anticarcinogenic mechanisms. There is considerable evidence that aberrant DNA methylation plays an important role in carcinogenesis. Furthermore, DNA methylation can be affected by dietary components. Therefore, in the present study, we investigated the DNA methylation status of CpG dinucleotides within the promoter region of the four genes protein kinase C o 1, ornithine decarboxylase 1, fos proto-oncogene and 5,10-methylenetetrahydrofolate reductase in the colon of female sporadic adenoma patients and healthy controls. These genes were chosen because their expression was modulated in response to altered vegetable intake, they are functionally relevant for CRC; they have CpG islands in their promoter region, and a methylation-specific restriction enzyme is available to permit quantitative assay. No significant differences in extent of methylation in colon DNA were detected for any of the four genes in both adenoma polyp patients and healthy controls after altering vegetable intake. Interestingly, before the intervention, ornithine decarboxylase 1 promoter methylation was lower in the colonic mucosa of the adenoma polyp patients when compared with healthy control subjects, which may explain the increased ornithine decarboxylase 1 activity in CRC reported in the literature. In conclusion, we found no evidence that changes in promoter methylation were responsible for differences in expression of four genes in the human colonic mucosa in response to altered vegetable intake. The mechanism(s) responsible for this altered gene expression and, indeed, potential effects on methylation of other genes remain to be determined.
机译:蔬菜可通过抗癌机制中涉及的基因表达变化来预防结直肠癌(CRC)。有大量证据表明异常的DNA甲基化在致癌过程中起着重要作用。此外,DNA甲基化会受到饮食成分的影响。因此,在本研究中,我们调查了雌性结肠中四个基因蛋白激酶C o 1,鸟氨酸脱羧酶1,fos原癌基因和5,10-亚甲基四氢叶酸还原酶的启动子区域内CpG二核苷酸的DNA甲基化状态。散发性腺瘤患者和健康对照。选择这些基因是因为它们的表达响应于蔬菜摄入量的变化而被调节,它们在功能上与CRC有关。它们在其启动子区域具有CpG岛,并且可以使用甲基化特异性限制酶进行定量分析。改变蔬菜摄入量后,在腺瘤息肉患者和健康对照者的四个基因中,未检测到结肠基因甲基化程度的显着差异。有趣的是,在干预之前,与健康对照组相比,腺瘤息肉患者结肠粘膜中鸟氨酸脱羧酶1启动子的甲基化程度较低,这可以解释文献中报道的鸟氨酸脱羧酶1活性增加。总之,我们发现没有证据表明启动子甲基化的变化是人类结肠粘膜响应于蔬菜摄入量变化的四个基因表达差异的原因。导致这种基因表达改变的机制以及对其他基因甲基化的潜在影响尚待确定。

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