Human Genetics Foundation (previously at ISI Foundation), Turin, Italy.
Cancer Epidemiol Biomarkers Prev. 2010 Dec;19(12):3174-81. doi: 10.1158/1055-9965.EPI-10-0314. Epub 2010 Oct 4.
Bulky DNA adducts are markers of exposure to genotoxic aromatic compounds, which reflect the ability of an individual to metabolically activate carcinogens and to repair DNA damage. Polycyclic aromatic hydrocarbons (PAHs) represent a major class of carcinogens that are capable of forming such adducts. Factors that have been reported to be related to DNA adduct levels include smoking, diet, body mass index (BMI), genetic polymorphisms, the season of collection of biologic material, and air pollutants.
We pooled 11 studies (3,600 subjects) in which bulky DNA adducts were measured in human white blood cells with similar (32)P-postlabeling techniques and for which a similar set of variables was available, including individual data on age, gender, ethnicity, batch, smoking habits, BMI, and season of blood collection, and a limited set of gene variants.
Lowest DNA adduct levels (P = 0.006) were observed in the spring (median = 0.50 adducts per 10(8) nucleotides), followed by summer (0.64), autumn (0.70), and winter (0.85). The same pattern emerged in multivariate analysis but only among never smokers (P = 0.02). Adduct levels were significantly lower (P = 0.001) in northern Europe (the Netherlands and Denmark; mean = 0.60, median = 0.40) than in southern Europe (Italy, Spain, France, and Greece; mean = 0.79, median = 0.60).
In this large pooled analysis, we have found only weak associations between bulky DNA adducts and exposure variables. Seasonality (with higher adducts levels in winter) and air pollution may partly explain some of the interarea differences (north vs. south Europe), but most inter-area and interindividual variations in adduct levels still remain unexplained.
Our study describes the largest pooled analysis of bulky DNA adducts so far, showing that interindividual variation is still largely unexplained, though seasonality seems to play a role.
大体积 DNA 加合物是暴露于遗传毒性芳香化合物的标志物,反映了个体代谢激活致癌物和修复 DNA 损伤的能力。多环芳烃 (PAH) 是一类主要的致癌物,能够形成这种加合物。据报道,与 DNA 加合物水平相关的因素包括吸烟、饮食、体重指数 (BMI)、遗传多态性、生物材料采集季节以及空气污染物。
我们汇集了 11 项研究(3600 名受试者),这些研究使用类似的 (32)P-后标记技术测量人体白细胞中的大体积 DNA 加合物,并且提供了类似的一组变量,包括年龄、性别、种族、批次、吸烟习惯、BMI 和血液采集季节的个体数据,以及有限的基因变体。
春季(中位数=0.50 个加合物/10(8)个核苷酸)观察到最低的 DNA 加合物水平(P=0.006),其次是夏季(0.64)、秋季(0.70)和冬季(0.85)。多变量分析也出现了相同的模式,但仅在从不吸烟者中(P=0.02)。欧洲北部(荷兰和丹麦;平均值=0.60,中位数=0.40)的加合物水平明显低于欧洲南部(意大利、西班牙、法国和希腊;平均值=0.79,中位数=0.60)(P=0.001)。
在这项大型综合分析中,我们只发现大体积 DNA 加合物与暴露变量之间存在微弱关联。季节性(冬季加合物水平较高)和空气污染可能部分解释了一些地区差异(北欧与南欧),但加合物水平的大多数地区间和个体间差异仍未得到解释。
本研究描述了迄今为止最大的大体积 DNA 加合物综合分析,表明个体间变异仍在很大程度上无法解释,尽管季节性似乎发挥了作用。