Barnicle Alan, Seoighe Cathal, Greally John M, Golden Aaron, Egan Laurence J
a Clinical Pharmacology, School of Medicine, National University of Ireland , Galway , Ireland.
b School of Mathematics, Statistics and Applied Mathematics, National University of Ireland , Galway , Ireland.
Epigenetics. 2017 Aug;12(8):591-606. doi: 10.1080/15592294.2017.1334023. Epub 2017 May 30.
Aberrant DNA methylation patterns have been reported in inflamed tissues and may play a role in disease. We studied DNA methylation and gene expression profiles of purified intestinal epithelial cells from ulcerative colitis patients, comparing inflamed and non-inflamed areas of the colon. We identified 577 differentially methylated sites (false discovery rate <0.2) mapping to 210 genes. From gene expression data from the same epithelial cells, we identified 62 differentially expressed genes with increased expression in the presence of inflammation at prostate cancer susceptibility genes PRAC1 and PRAC2. Four genes showed inverse correlation between methylation and gene expression; ROR1, GXYLT2, FOXA2, and, notably, RARB, a gene previously identified as a tumor suppressor in colorectal adenocarcinoma as well as breast, lung and prostate cancer. We highlight targeted and specific patterns of DNA methylation and gene expression in epithelial cells from inflamed colon, while challenging the importance of epithelial cells in the pathogenesis of chronic inflammation.
炎症组织中已报道存在异常的DNA甲基化模式,其可能在疾病中发挥作用。我们研究了溃疡性结肠炎患者纯化的肠上皮细胞的DNA甲基化和基因表达谱,比较了结肠的炎症区域和非炎症区域。我们鉴定出577个差异甲基化位点(错误发现率<0.2),这些位点映射到210个基因。从相同上皮细胞的基因表达数据中,我们在前列腺癌易感基因PRAC1和PRAC2存在炎症的情况下,鉴定出62个表达增加的差异表达基因。四个基因显示甲基化与基因表达呈负相关;ROR1、GXYLT2、FOXA2,值得注意的是还有RARB,该基因先前在结直肠癌以及乳腺癌、肺癌和前列腺癌中被鉴定为肿瘤抑制基因。我们强调了炎症结肠上皮细胞中DNA甲基化和基因表达的靶向性和特异性模式,同时对上皮细胞在慢性炎症发病机制中的重要性提出了质疑。