Harlid Sophia, Xu Zongli, Panduri Vijayalakshmi, Sandler Dale P, Taylor Jack A
Laboratory of Molecular Carcinogenesis, and.
Environ Health Perspect. 2014 Jul;122(7):673-8. doi: 10.1289/ehp.1307480. Epub 2014 Apr 4.
Smoking increases the risk of many diseases, and it is also linked to blood DNA methylation changes that may be important in disease etiology.
We sought to identify novel CpG sites associated with cigarette smoking.
We used two epigenome-wide data sets from the Sister Study to identify and confirm CpG sites associated with smoking. One included 908 women with methylation measurements at 27,578 CpG sites using the HumanMethylation27 BeadChip; the other included 200 women with methylation measurements for 473,844 CpG sites using the HumanMethylation450 BeadChip. Significant CpGs from the second data set that were not included in the 27K assay were validated by pyrosequencing in a subset of 476 samples from the first data set.
Our study successfully confirmed smoking associations for 9 previously established CpGs and identified 2 potentially novel CpGs: cg26764244 in GNG12 (p = 9.0 × 10-10) and cg22335340 in PTPN6 (p = 2.9 × 10-05). We also found strong evidence of an association between smoking status and cg02657160 in CPOX (p = 7.3 × 10-7), which has not been previously reported. All 12 CpGs were undermethylated in current smokers and showed an increasing percentage of methylation in former and never-smokers.
We identified 2 potentially novel smoking related CpG sites, and provided independent replication of 10 previously reported CpGs sites related to smoking, one of which is situated in the gene CPOX. The corresponding enzyme is involved in heme biosynthesis, and smoking is known to increase heme production. Our study extends the evidence base for smoking-related changes in DNA methylation.
吸烟会增加多种疾病的风险,并且还与血液DNA甲基化变化有关,这些变化可能在疾病病因学中具有重要意义。
我们试图识别与吸烟相关的新的CpG位点。
我们使用了姐妹研究中的两个全表观基因组数据集来识别和确认与吸烟相关的CpG位点。一个数据集包含908名女性,她们使用HumanMethylation27 BeadChip对27,578个CpG位点进行了甲基化测量;另一个数据集包含200名女性,她们使用HumanMethylation450 BeadChip对473,844个CpG位点进行了甲基化测量。通过焦磷酸测序在第一个数据集的476个样本子集中对第二个数据集中未包含在27K检测中的显著CpG进行了验证。
我们的研究成功确认了9个先前确定的与吸烟相关的CpG位点,并识别出2个潜在的新CpG位点:GNG12中的cg26764244(p = 9.0 × 10-10)和PTPN6中的cg22335340(p = 2.9 × 10-05)。我们还发现有强有力的证据表明吸烟状态与CPOX中的cg02657160之间存在关联(p = 7.3 × 10-7),此前尚未有相关报道。所有12个CpG在当前吸烟者中甲基化程度较低,而在前吸烟者和从不吸烟者中甲基化百分比呈上升趋势。
我们识别出2个潜在的与吸烟相关的新CpG位点,并对10个先前报道的与吸烟相关的CpG位点进行了独立验证,其中一个位于CPOX基因中。相应的酶参与血红素生物合成,已知吸烟会增加血红素生成。我们的研究扩展了与吸烟相关的DNA甲基化变化的证据基础。