Møller Peter, Collins Andrew, Rodriguez-Garraus Adriana, Langie Sabine A S, Godschalk Roger, Azqueta Amaya
Department of Public Health, Section of Environmental Health, University of Copenhagen, Øster Farimagsgade 5A, DK-1014 Copenhagen K, Denmark.
Department of Nutrition, University of Oslo, Oslo, Norway.
Mutagenesis. 2025 Apr 24;40(2):99-110. doi: 10.1093/mutage/geaf004.
In the comet assay, DNA damage is assessed by differences in DNA migration from gel-embedded nucleoids. Even a small difference in DNA migration between exposure groups can be statistically significant but may invite speculation about the biological significance of such slight increases in DNA migration. A small difference can be defined as a net difference of 1-2% Tail DNA, but background levels of DNA migration typically vary already more than 1-2% Tail DNA between studies. Here, we have used studies on ionizing radiation to assess the lowest detectable differences in DNA migration; variation in exposure-effect relationships; variation in central tendencies of DNA migration; unsystematic (residual) variation; and the actual number of lesions detectable with the comet assay. A total of 51 studies on ionizing radiation exposure in mammalian cells have been systematically reviewed, including results from ring-trial studies where the same batch of irradiated cells has been analysed in different laboratories. Ring-trial studies have shown that unsystematic variation is approximately 4% Tail DNA in studies on ionizing radiation. Studies on ionizing radiation in cell cultures have shown statistically significant effects when the net increase of DNA migration is 0.3-3.1% Tail DNA. Among those experiments, the ones with optimal assay conditions to detect low levels of DNA damage show statistically significant effects with doses of around 0.30 Gy, which corresponds to approximately 350 lesions per diploid cell. However, it has also been shown that the same dose of ionizing radiation can give rise to different levels of DNA migration (i.e. 0.7-7.8% Tail DNA per Gy) in different studies. In summary, the results show that even a small statistically significant difference in DNA migration has biological significance within the same experiment, but comparisons of DNA migration values between studies have limited biological implications.
在彗星试验中,通过凝胶包埋的核小体中DNA迁移的差异来评估DNA损伤。即使暴露组之间DNA迁移的差异很小,在统计学上也可能具有显著性,但这可能会引发对这种DNA迁移轻微增加的生物学意义的猜测。小差异可定义为尾DNA净差异为1 - 2%,但在不同研究中,DNA迁移的背景水平通常已经有超过1 - 2%尾DNA的变化。在此,我们利用关于电离辐射的研究来评估DNA迁移中可检测到的最低差异;暴露-效应关系的变化;DNA迁移集中趋势的变化;非系统性(残余)变化;以及彗星试验可检测到的实际损伤数量。总共系统回顾了51项关于哺乳动物细胞电离辐射暴露的研究,包括环试研究的结果,在环试研究中,同一批受辐照细胞在不同实验室进行了分析。环试研究表明,在电离辐射研究中,非系统性变化约为4%尾DNA。细胞培养中关于电离辐射的研究表明,当DNA迁移净增加为0.3 - 3.1%尾DNA时,具有统计学显著效应。在这些实验中,那些具有检测低水平DNA损伤的最佳试验条件的实验,在剂量约为0.30 Gy时显示出统计学显著效应,这相当于每个二倍体细胞约350个损伤。然而,也已表明,相同剂量的电离辐射在不同研究中可导致不同水平的DNA迁移(即每Gy为0.7 - 7.8%尾DNA)。总之,结果表明,即使DNA迁移中一个小的统计学显著差异在同一实验中具有生物学意义,但不同研究之间DNA迁移值的比较具有有限的生物学意义。