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Gene hypermethylation in blood leukocytes in humans long term after radiation exposure - Validation set

机译:辐射暴露后长期人类血液白细胞中的基因高甲基化-验证集

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Hypermethylation of CpG islands in the promoter regions of several genes with basic protective function in blood leukocytes of individuals exposed to ionizing radiation long time ago (2-46 years), and differential effects of age and radiation exposure on hypermethylation was reported in our previous work. To validate these results, epigenetic modifications were assessed in an independent series of 49 nuclear industry workers from the "Mayak" facility (67-84 years old at sampling) with documented individual accumulated doses from the prolonged external gamma-radiation exposure (95.9-409.5 cGy, end of work with radiation:0.3-39 years ago), and in 50 non-exposed persons matched by age. In addition to the genes analyzed before (RASSF1A, p16/INK4A, p14/ARF, GSTP1), four additional loci were analyzed: TP53, ATM, SOD3, ESR1. The frequency of individuals displaying promoter methylation of at least one of the 8 genes (71.4%) was significantly higher in exposed group as compared to the control group (40%), p = .002, OR = 3.75. A significantly elevated frequency of individuals with hypermethylated CpG islands in GSTP1, TP53, SOD3 promoters was revealed among exposed subjects as compared to the control group (p = .012, OR = 8.41; p = .041, OR = 4.02 and p = .009, OR = 3.42, respectively). A similar trend (p = .12, OR = 3.06) was observed for the p16/INK4A gene. As a whole, p16/INK4A and GSTP1 promoter hypermethylation in irradiated subjects from both previously and currently analyzed groups was pronounced. Thus, the direction of the effects was fully confirmed, suggesting the result reproducibility. No statistically significant correlation between promoter methylation and individual radiation dose was found. Further studies are required to create an array of blood epigenetic markers of radiation exposure associating with premature aging and age-related diseases and to accurately evaluate radiation-added effect across the range of doses.
机译:在很久以前(2-46年)暴露于电离辐射的个体的血液白细胞中,几个具有基本保护功能的基因的启动子区域中的CpG岛超甲基化,并且在我们以前的工作中报道了年龄和辐射暴露对超甲基化的不同影响。为了验证这些结果,在来自“ Mayak”设施的49名核工业工人的独立系列中评估了表观遗传修饰(抽样时年龄67-84岁),并记录了长时间的外部伽马辐射暴露引起的个体累积剂量(95.9-409.5) cGy,有辐射的工作结束:0.3-39年前),并按年龄匹配了50名未暴​​露人群。除了之前分析的基因(RASSF1A,p16 / INK4A,p14 / ARF,GSTP1)外,还分析了另外四个基因座:TP53,ATM,SOD3,ESR1。与对照组(40%)相比,暴露组的8个基因中至少一个显示启动子甲基化的个体频率(71.4%)显着更高,p = .002,OR = 3.75。与对照组相比,暴露的受试者中GSTP1,TP53,SOD3启动子中具有高甲基化CpG岛的个体的频率显着升高(p = .012,OR = 8.41; p = .041,OR = 4.02和p =。 009,或= 3.42)。对于p16 / INK4A基因,观察到相似的趋势(p = .12,OR = 3.06)。总体而言,在先前和当前分析组的受辐照受试者中,p16 / INK4A和GSTP1启动子的甲基化程度都很高。因此,充分证实了作用的方向,表明了结果的可重复性。在启动子甲基化和单独的辐射剂量之间未发现统计学上显着的相关性。需要开展进一步的研究,以建立一系列与早衰和与年龄有关的疾病相关的辐射暴露的血液表观遗传标记,并准确评估整个剂量范围内的辐射增加效应。

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