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[散发性和遗传性结直肠癌中的DNA甲基化缺陷]

[DNA methylation defects in sporadic and hereditary colorectal cancer].

作者信息

Xicola Rosa M, Llor Xavier

机构信息

Univerisity of Illinois at Chicago, Digestive Disease and Nutrition, Chicago, IL, USA.

出版信息

Gastroenterol Hepatol. 2012 Aug-Sep;35(7):480-7. doi: 10.1016/j.gastrohep.2012.01.010. Epub 2012 Mar 27.

Abstract

DNA methylation is a fundamental epigenetic mechanism in regulating the expression of genes controlling crucial cell functions in cancer development. Methylation defects (both global hypomethylation and hypermethylation of CpG islands) are implicated in colorectal carcinogenesis. Some nutrients have a clear effect on methylation, suggesting that some dietary-associated differences in the incidence of colorectal cancer could be due to the effect of diet on methylation. The presence of methylation defects has clear diagnostic and prognostic implications. Thus, several tests are being used for colorectal cancer screening based on methylated gene analysis, whether in feces or blood. In addition, the reversibility of methylation processes allows the development of chemotherapies that regulate this process through their antineoplastic activity.

摘要

DNA甲基化是一种基本的表观遗传机制,在调控控制癌症发展中关键细胞功能的基因表达方面发挥作用。甲基化缺陷(包括整体低甲基化和CpG岛的高甲基化)与结直肠癌的发生有关。一些营养素对甲基化有明显影响,这表明结直肠癌发病率中一些与饮食相关的差异可能归因于饮食对甲基化的影响。甲基化缺陷的存在具有明确的诊断和预后意义。因此,基于甲基化基因分析,无论在粪便还是血液中,都有几种检测方法被用于结直肠癌筛查。此外,甲基化过程的可逆性使得通过其抗肿瘤活性来调节这一过程的化疗得以发展。

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