Identification of DNA methylation biomarkers for evaluating cardiovascular disease risk from epigenome profiles altered by low-dose ionizing radiation

被引:1
作者
Park, Jihye [1 ]
Lee, Hae-June [2 ]
Han, Yu Kyeong [3 ]
Kang, Keunsoo [1 ]
Yi, Joo Mi [3 ]
机构
[1] Dankook Univ, Dept Microbiol, Cheonan 31116, South Korea
[2] Korea Inst Radiol & Med Sci, Div Radiat Biomed Res, Seoul 01812, South Korea
[3] Inje Univ, Coll Med, Dept Microbiol & Immunol, Busan 47392, South Korea
基金
新加坡国家研究基金会;
关键词
DNA methylation; Low-dose radiation; Human aortic endothelial cells (HAECs); Methylation biomarker; Assessment of cardiovascular risk; ATOMIC-BOMB SURVIVORS; GENE-EXPRESSION; HEART-DISEASE; CANCER; ASSOCIATION; PGRMC1; MAINTENANCE; FAD104; TARGET; DNMT3B;
D O I
10.1186/s13148-024-01630-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Environmental exposure, medical diagnostic and therapeutic applications, and industrial utilization of radionuclides have prompted a growing focus on the risks associated with low-dose radiation (< 100 mGy). Current evidence suggests that such radiation can induce epigenetic changes. Nevertheless, whether exposure to low-dose radiation can disrupt endothelial cell function at the molecular level is unclear. Because endothelial cells play crucial roles in cardiovascular health and disease, we aimed to investigate whether low-dose radiation could lead to differential DNA methylation patterns at the genomic level in endothelial cell (EC) lines. Methods We screened for changes in DNA methylation patterns in primary human aortic (HAECs) and coronary artery endothelial cells following exposure to low-dose ionizing radiation. Using a subset of genes altered via DNA methylation by low-dose irradiation, we performed gene ontology (GO) analysis to predict the possible biological network mediating the effect of low-dose radiation. In addition, we performed comprehensive validation using methylation and gene expression analyses, and ChIP assay to identify useful biomarkers among candidate genes for use in detecting low-dose radiation exposure in human primary normal ECs. Results Low-dose radiation is sufficient to induce global DNA methylation alterations in normal EC lines. GO analysis demonstrated that these hyper- or hypo-methylated genes were linked to diverse biological pathways. Our findings indicated a robust correlation between promoter hypermethylation and transcriptional downregulation of four genes (PGRMC1, UNC119B, RERE, and FNDC3B) in response to low-dose ionizing radiation in HAECs. Conclusions Based on these findings, the identified genes can serve as potential DNA methylation biomarkers for the assessment of cardiovascular risk upon exposure to low-dose radiation.
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页数:15
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