Peplonska Beata, Bukowska Agnieszka, Wieczorek Edyta, Przybek Monika, Zienolddiny Shanbeh, Reszka Edyta
Department of Environmental Epidemiology, Nofer Institute of Occupational Medicine, Lodz, Poland.
Department of Molecular Genetics and Epigenetics, Nofer Institute of Occupational Medicine, Lodz, Poland.
PLoS One. 2017 Jun 8;12(6):e0178792. doi: 10.1371/journal.pone.0178792. eCollection 2017.
Some recent evidence suggests that environmental and lifestyle factors may modify DNA methylation. We hypothesized that rotating night work and several modifiable factors may be associated with the methylation of the promoter regions within two tumor suppressor and DNA repair genes: BRCA1 and BRCA2. The methylation status of BRCA1 and BRCA2 was determined via qMSP reactions using DNA samples derived from blood leucocytes of 347 nurses and midwives working rotating nights and 363 working during the days. The subjects were classified into unmethylated vs methylated BRCA1 and BRCA2 when the methylation index was 0% or >0%, respectively. The adjusted odds ratios with 95% confidence intervals were calculated for night work status, smoking, obesity, physical activity and alcohol drinking. Current night shift work or night work history was not associated with methylation status of the promoter sites within BRCA1 and BRCA2 genes. We observed weak associations between smoking and the methylation status of BRCA1 with OR = 1.50 (95%CI: 0.98-2.29) for current smoking, OR = 1.83, 95CI: 1.08-3.13 for smoking longer than 31 years, and 0.1>p>0.05 for trends for the number of cigarettes per day, smoking duration and packyears. In conclusion, no links between night shift work and methylation of the promoter region within the BRCA1, and BRCA2 genes were observed in this exploratory analysis. The findings of our study weakly support the hypothesis that smoking may contribute to epigenetic events.
最近的一些证据表明,环境和生活方式因素可能会改变DNA甲基化。我们推测,轮班工作和一些可改变的因素可能与两个肿瘤抑制和DNA修复基因(BRCA1和BRCA2)启动子区域的甲基化有关。通过定量甲基化特异性PCR反应,使用来自347名轮班工作的护士和助产士以及363名日间工作者的血液白细胞DNA样本,确定BRCA1和BRCA2的甲基化状态。当甲基化指数分别为0%或>0%时,将受试者分为BRCA1和BRCA2未甲基化组与甲基化组。计算夜班工作状态、吸烟、肥胖、体力活动和饮酒的调整比值比及95%置信区间。当前的夜班工作或夜班工作史与BRCA1和BRCA2基因启动子位点的甲基化状态无关。我们观察到吸烟与BRCA1甲基化状态之间存在微弱关联,当前吸烟者的OR = 1.50(95%CI:0.98 - 2.29),吸烟超过31年者的OR = 1.83,95%CI:1.08 - 3.13,且每日吸烟量、吸烟持续时间和吸烟包年数的趋势p值在0.1>p>0.05之间。总之,在这项探索性分析中,未观察到夜班工作与BRCA1和BRCA2基因启动子区域甲基化之间的联系。我们研究的结果微弱支持吸烟可能导致表观遗传事件的假设。