Liang Ying, Fu Qibin, Wang Xudong, Liu Feng, Yang Gen, Luo Chunxiong, Ouyang Qi, Wang Yugang
State Key Laboratory of Nuclear Physics and Technology, School of Physics, Peking University, Beijing 100871, People's Republic of China.
Phys Med Biol. 2017 Mar 21;62(6):2153-2175. doi: 10.1088/1361-6560/aa56ed. Epub 2017 Jan 5.
Current knowledge in radiobiology ascribes the adverse biological effects of ionizing radiation primarily to the induction of DNA double-strand breaks (DSBs), which is supposed to be potentially lethal and may be converted to lethal damage due to misrepair. Soft and ultrasoft x-rays have been found to bear elevated biological effectiveness for cell killing compared with conventional x-rays or Co γ-rays. This phenomenon is qualitatively interpreted as the increased level of DSB induction for low energy photons, however, a thorough quantitative reasoning is lacking. Here, we systematically compared the relative biological effectiveness (RBE) with relative DSB induction for photons from several hundreds of eV up to MeV. Although there is an approximate two-fold increase in the yields of DSB for low energy photons found in our calculation and a large number of experimental measurements, it is far from enough to account for the three- to four-fold increase in RBE. Further theoretical investigations show that DSB complexity (additional single-strand breaks and base damage within 10 base pairs) increases notably for low energy photons, which largely reconciles the discrepancy between RBE and DSB induction. Our theoretical results are in line with accumulating experimental evidence that complex DSBs are refractory to repair machinery and may contribute predominantly to the formation of lethal damage.
放射生物学的现有知识将电离辐射的不良生物学效应主要归因于DNA双链断裂(DSB)的诱导,这种断裂被认为具有潜在致死性,并且可能由于错误修复而转化为致死性损伤。与传统X射线或钴γ射线相比,已发现软X射线和极软X射线对细胞杀伤具有更高的生物学效能。这种现象定性地解释为低能光子诱导DSB的水平增加,然而,缺乏全面的定量推理。在这里,我们系统地比较了从几百电子伏特到兆电子伏特的光子的相对生物学效能(RBE)与相对DSB诱导。尽管在我们的计算和大量实验测量中发现低能光子的DSB产率大约增加了两倍,但这远远不足以解释RBE增加三到四倍的情况。进一步的理论研究表明,低能光子的DSB复杂性(10个碱基对内的额外单链断裂和碱基损伤)显著增加,这在很大程度上解释了RBE和DSB诱导之间的差异。我们的理论结果与越来越多的实验证据一致,即复杂的DSB难以被修复机制修复,并且可能主要导致致死性损伤的形成。