Department of Community and Family Medicine, Geisel School of Medicine at Dartmouth College, Lebanon, NH, USA.
Department of Pathology, Dartmouth-Hitchcock Medical Center, Lebanon, NH, USA.
Mod Pathol. 2014 Jan;27(1):145-55. doi: 10.1038/modpathol.2013.104. Epub 2013 Jul 19.
Recent studies have shown two distinct non-CIMP methylation clusters in colorectal cancer, raising the possibility that DNA methylation, involving non-CIMP genes, may play a role in the conventional adenoma-carcinoma pathway. A total of 135 adenomas (65 left colon and 70 right colon) were profiled for epigenome-wide DNA methylation using the Illumina HumanMethylation450 BeadChip. A principal components analysis was performed to examine the association between variability in DNA methylation and adenoma location. Linear regression and linear mixed effects models were used to identify locus-specific differential DNA methylation in adenomas of right and left colon. A significant association was present between the first principal component and adenoma location (P=0.007), even after adjustment for subject age and gender (P=0.009). A total of 168 CpG sites were differentially methylated between right- and left-colon adenomas and these loci demonstrated enrichment of homeobox genes (P=3.0 × 10(-12)). None of the 168 probes were associated with CIMP genes. Among CpG loci with the largest difference in methylation between right- and left-colon adenomas, probes associated with PRAC (prostate cancer susceptibility candidate) gene showed hypermethylation in right-colon adenomas whereas those associated with CDX2 (caudal type homeobox transcription factor 2) showed hypermethylation in left-colon adenomas. A subgroup of left-colon adenomas enriched for current smokers (OR=6.1, P=0.004) exhibited a methylation profile similar to right-colon adenomas. In summary, our results indicate distinct patterns of DNA methylation, independent of CIMP genes, in adenomas of the right and left colon.
最近的研究表明,结直肠癌中有两个不同的非 CIMP 甲基化簇,这使得非 CIMP 基因涉及的 DNA 甲基化可能在传统的腺瘤-癌途径中发挥作用。总共对 135 个腺瘤(65 个左结肠和 70 个右结肠)进行了全基因组表观遗传 DNA 甲基化分析,使用了 Illumina HumanMethylation450 BeadChip。进行了主成分分析,以检查 DNA 甲基化变异性与腺瘤位置之间的关联。使用线性回归和线性混合效应模型来识别右和左结肠腺瘤中特定位置的差异 DNA 甲基化。第一主成分与腺瘤位置之间存在显著关联(P=0.007),即使在调整了受试者年龄和性别后(P=0.009)也是如此。右结肠和左结肠腺瘤之间存在 168 个 CpG 位点的差异甲基化,这些基因座显示同源盒基因的富集(P=3.0×10(-12))。在右结肠和左结肠腺瘤之间甲基化差异最大的 168 个探针中,与 PRAC(前列腺癌易感性候选基因)基因相关的探针在右结肠腺瘤中表现出过度甲基化,而与 CDX2(尾型同源盒转录因子 2)相关的探针在左结肠腺瘤中表现出过度甲基化。富含当前吸烟者的左结肠腺瘤亚组(OR=6.1,P=0.004)表现出与右结肠腺瘤相似的甲基化谱。总之,我们的结果表明,右结肠和左结肠腺瘤中的 DNA 甲基化模式存在明显的差异,独立于 CIMP 基因。