Cho Yoon Hee, Jang Yoonhee, Woo Hae Dong, Kim Yang Jee, Kim Su Young, Christensen Sonja, Cole Elizabeth, Choi Soo Yong, Chung Hai Won
Department of Biomedical and Pharmaceutical Sciences, University of Montana, Missoula, Montana.
Department of Psychology, The University of Montana, Missoula, Montana.
Environ Mol Mutagen. 2019 Mar;60(2):174-184. doi: 10.1002/em.22237. Epub 2018 Nov 29.
Global DNA hypomethylation is proposed as a potential biomarker for cancer risk associated with genomic instability, which is an important factor in radiation-induced cancer. However, the associations among radiation exposure, changes in DNA methylation, and carcinogenesis are unclear. The aims of this study were (1) to examine whether low-level occupational radiation exposure induces genomic DNA hypomethylation; and (2) to determine the relationships between radiation exposure, genomic DNA hypomethylation and radiation-induced genomic instability (RIGI) in industrial radiographers. Genomic DNA methylation levels were measured in blood DNA from 40 radiographers and 28 controls using the LINE-1 pyrosequencing assay and the luminometric methylation assay. Further, the micronucleus-centromere assay was performed to measure aneuploidy of chromosomes 1 and 4 as a marker of delayed RIGI. Genomic DNA methylation levels were significantly lower in radiographers than those in controls. LINE-1 hypomethylation was not significantly correlated with recent 1-year, recent 3-year, or total cumulative radiation doses in radiographers; however, LINE-1 hypomethylation significantly correlated with the cumulative radiation dose without recent 3-year exposure data (D3dose, r = -0.39, P < 0.05). In addition, LINE-1 hypomethylation was a significant contributor to aneuploidy frequency by D3dose (F (2, 34) = 13.85, P < 0.001), in which a total of 45% of the variance in aneuploidy frequency was explained. Our results provide suggestive evidence regarding the delayed effects of low-dose occupational radiation exposure in radiographers and its association with LINE-1 hypomethylation; however, additional studies using more subjects are needed to fully understand the relationship between genomic DNA hypomethylation and RIGI. Environ. Mol. Mutagen. 60: 174-184, 2019. © 2018 Wiley Periodicals, Inc.
全球DNA低甲基化被认为是与基因组不稳定相关的癌症风险的潜在生物标志物,而基因组不稳定是辐射诱发癌症的一个重要因素。然而,辐射暴露、DNA甲基化变化与致癌作用之间的关联尚不清楚。本研究的目的是:(1)检测低水平职业辐射暴露是否会导致基因组DNA低甲基化;(2)确定工业放射技师中辐射暴露、基因组DNA低甲基化与辐射诱发的基因组不稳定(RIGI)之间的关系。使用LINE-1焦磷酸测序法和发光甲基化检测法,对40名放射技师和28名对照者血液DNA中的基因组DNA甲基化水平进行了测量。此外,进行了微核-着丝粒检测,以测量1号和4号染色体的非整倍体,作为延迟RIGI的标志物。放射技师的基因组DNA甲基化水平显著低于对照组。LINE-1低甲基化与放射技师最近1年、最近3年或总累积辐射剂量无显著相关性;然而,LINE-1低甲基化与无最近3年暴露数据的累积辐射剂量(D3剂量)显著相关(r = -0.39,P < 0.05)。此外,LINE-1低甲基化是D3剂量导致非整倍体频率的一个重要因素(F(2, 34) = 13.85,P < 0.001),其中非整倍体频率45%的方差可由此解释。我们的结果为低剂量职业辐射暴露对放射技师的延迟影响及其与LINE-1低甲基化的关联提供了提示性证据;然而,需要更多受试者参与的进一步研究,以充分了解基因组DNA低甲基化与RIGI之间的关系。《环境与分子诱变》2019年第60卷:174 - 184页。© 2018威利期刊公司