| Literature DB >> 28143891 |
Tzu-Pin Lu1, Nai-Chen Chuang1, Chin-Yu Cheng2, Cheng-An Hsu2, Yi-Chih Wang3, Yen-Hong Lin3, Jen-Kuang Lee3, Cho-Kai Wu3, Juey-Jen Hwang3, Lian-Yu Lin3, Shih-Fan Sherri Yeh4,5, Kuo-Liang Chien1, Jyh-Ming Jimmy Juang6.
Abstract
Coronary artery ectasia (CAE) is a disease characterized by abnormally dilated coronary arteries. The mechanism of CAE remains unclear, and its treatment is limited. Previous studies have shown that risk factors for CAE were related to changes in DNA methylation. However, no systematic investigation of methylation profiles has been performed. Therefore, we compared methylation profiles between 12 CAE patients and 12 propensity-matched individuals with normal coronary arteries using microarrays. Wilcoxon's rank sum tests revealed 89 genes with significantly different methylation levels (P<0.05 and Δβ > |0.1|). Functional characterization using the DAVID database and gene set enrichment analysis indicated that these genes were involved in immune and inflammatory responses. Of these genes 6 were validated in 29 CAE patients and 87 matched individuals with CAE, using pyro-sequencing. TLR6 and NOTCH4 showed significant differences in methylation between the two groups, and lower protein levels of toll-like receptor 6 (TLR6) were detected in CAE patients. In conclusion, this genome-wide analysis of methylation profiles in CAE patients showed that significant changes in both methylation and expression of TLR6 deserve further study to elucidate their roles in CAE.Entities:
Keywords: TLR6; coronary artery ectasia; methylation; microarray
Mesh:
Substances:
Year: 2017 PMID: 28143891 DOI: 10.1042/CS20160821
Source DB: PubMed Journal: Clin Sci (Lond) ISSN: 0143-5221 Impact factor: 6.124