Institute of Cell Biology (Cancer Research), University of Duisburg-Essen, Medical School, Virchowstrasse 173, 45122 Essen, Germany.
Department of Therapeutic Radiology, Yale University School of Medicine, 15 York Street, New Haven, CT 06520, USA.
Int J Mol Sci. 2018 Nov 28;19(12):3779. doi: 10.3390/ijms19123779.
Proton beam therapy is increasingly applied for the treatment of human cancer, as it promises to reduce normal tissue damage. However, little is known about the relationship between linear energy transfer (LET), the type of DNA damage, and cellular repair mechanisms, particularly for cells irradiated with protons. We irradiated cultured cells delivering equal doses of X-ray photons, Bragg-peak protons, or plateau protons and used this set-up to quantitate initial DNA damage (mainly DNA double strand breaks (DSBs)), and to analyze kinetics of repair by detecting γH2A.X or 53BP1 using immunofluorescence. The results obtained validate the reliability of our set-up in delivering equal radiation doses under all conditions employed. Although the initial numbers of γH2A.X and 53BP1 foci scored were similar under the different irradiation conditions, it was notable that the maximum foci level was reached at 60 min after irradiation with Bragg-peak protons, as compared to 30 min for plateau protons and photons. Interestingly, Bragg-peak protons induced larger and irregularly shaped γH2A.X and 53BP1 foci. Additionally, the resolution of these foci was delayed. These results suggest that Bragg-peak protons induce DNA damage of increased complexity which is difficult to process by the cellular repair apparatus.
质子束疗法越来越多地应用于人类癌症的治疗,因为它有望减少正常组织的损伤。然而,对于与线性能量传递(LET)、DNA 损伤类型和细胞修复机制的关系,特别是对于用质子照射的细胞,人们知之甚少。我们用 X 射线光子、布拉格峰质子或平台质子照射培养的细胞,并采用这种方法来定量分析初始 DNA 损伤(主要是 DNA 双链断裂(DSB)),通过免疫荧光检测 γH2A.X 或 53BP1 来分析修复动力学。所得到的结果验证了我们的设置在所有使用的条件下都能可靠地输送等量的辐射剂量。尽管在不同的照射条件下,最初检测到的 γH2A.X 和 53BP1 焦点数量相似,但值得注意的是,与平台质子和光子相比,用布拉格峰质子照射后 60 分钟达到最大焦点水平,而达到最大焦点水平的时间为 30 分钟。有趣的是,布拉格峰质子诱导形成更大且形状不规则的 γH2A.X 和 53BP1 焦点。此外,这些焦点的分辨率延迟。这些结果表明,布拉格峰质子诱导的 DNA 损伤复杂性增加,这使得细胞修复装置难以处理。