Department of Environment and Primary Prevention, Istituto Superiore diSanità, V.le Regina Elena 299, 00161 Rome, Italy.
Mutagenesis. 2013 Mar;28(2):135-44. doi: 10.1093/mutage/ges062. Epub 2012 Nov 6.
Previous studies in twins indicate that non-shared environment, beyond genetic factors, contributes substantially to individual variation in mutagen sensitivity; however, the role of specific causative factors (e.g. tobacco smoke, diet) was not elucidated. In this investigation, a population of 22 couples of monozygotic twins with discordant smoking habits was selected with the aim of evaluating the influence of tobacco smoke on individual response to DNA damage. The study design virtually eliminated the contribution of genetic heterogeneity to the intra-pair variation in DNA damage response, and thus any difference in the end-points investigated could directly be attributed to the non-shared environment experienced by co-twins, which included as main factor cigarette smoke exposure. Peripheral lymphocytes of study subjects were challenged ex vivo with γ-rays, and the induction, processing, fixation of DNA damage evaluated through multiple approaches. Folate status of study subjects was considered significant covariate since it is affected by smoking habits and can influence radiosensitivity. Similar responses were elicited by γ-rays in co-twins for all the end-points analysed, despite their discordant smoking habits. Folate status did not modify DNA damage response, even though a combined effect of smoking habits, low-plasma folic acid level, and ionising radiation was observed on apoptosis. A possible modulation of DNA damage response by duration and intensity of tobacco smoke exposure was suggested by Comet assay and micronucleus data, but the effect was quantitatively limited. Overall, the results obtained indicate that differences in smoking habits do not contribute to a large extent to inter-individual variability in the response to radiation-induced DNA damage observed in healthy human populations.
先前的双胞胎研究表明,除遗传因素外,非共享环境对诱变敏感性的个体差异有很大贡献;然而,特定致病因素(如烟草烟雾、饮食)的作用尚不清楚。在这项研究中,选择了 22 对具有不同吸烟习惯的同卵双胞胎夫妇的人群,目的是评估烟草烟雾对个体对 DNA 损伤反应的影响。该研究设计实际上消除了遗传异质性对 DNA 损伤反应个体内变异的贡献,因此,所研究终点的任何差异都可以直接归因于同卵双胞胎所经历的非共享环境,其中主要因素是香烟烟雾暴露。研究对象的外周淋巴细胞在体外受到 γ 射线的挑战,通过多种方法评估 DNA 损伤的诱导、加工和固定。研究对象的叶酸状态被认为是一个重要的协变量,因为它受吸烟习惯的影响,并可能影响放射敏感性。尽管双胞胎的吸烟习惯不同,但 γ 射线在同卵双胞胎中引起了所有终点的相似反应。叶酸状态并没有改变 DNA 损伤反应,尽管吸烟习惯、低血浆叶酸水平和电离辐射对细胞凋亡有联合作用。彗星试验和微核数据表明,烟草烟雾暴露的持续时间和强度可能对 DNA 损伤反应有一定的调节作用,但这种作用在数量上是有限的。总的来说,研究结果表明,吸烟习惯的差异在很大程度上不会导致健康人群对辐射诱导的 DNA 损伤反应的个体差异。