首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >From Energy Deposition of Ionizing Radiation to Cell Damage Signaling: Benchmarking Simulations by Measured Yields of Initial DNA Damage after Ion Microbeam Irradiation
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From Energy Deposition of Ionizing Radiation to Cell Damage Signaling: Benchmarking Simulations by Measured Yields of Initial DNA Damage after Ion Microbeam Irradiation

机译:从电离辐射的能量沉积到细胞损伤信令:通过测量的初始DNA辐照后测量的初始DNA损伤的产生基准仿真

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Advances in accelerator technology, which have enabled conforming radiotherapy with charged hadronic species, have brought benefits as well as potential new risks to patients. To better understand the effects of ionizing radiation on tumor and surrounding tissue, it is important to investigate and quantify the relationship between energy deposition at the nanometric scale and the initial biological events. Monte Carlo track structure simulation codes provide a powerful tool for investigating this relationship; however, their success and reliability are dependent on their improvement and development accordingly to the dedicated biological data to which they are challenged. For this aim, a microbeam facility that allows for (Thence control, down to one ion per cell nucleus, was used to evaluate relative frequencies of DNA damage after interaction between the incoming ion and DNA according to radiation quality. Primary human cells were exposed to alpha particles of three different energies with respective linear energy transfers (LETs) of approximately 36, 85 or 170 keV.mu m(-1) at the cells' center position, or to protons (19 keV.mu m(-1)). Statistical evaluation of nuclear foci formation (53BP1/gamma-H2AX), observed using immunofluorescence and related to a particle traversal, was undertaken in a large population of cell nuclei. The biological results were adjusted to consider the factors that drive the experimental uncertainties, then challenged with results using Geant4-DNA code modeling of the ionizing particle interactions on a virtual phantom of the cell nucleus with the same mean geometry and DNA density as the cells used in our experiments. Both results showed an increase of relative frequencies of foci (or simulated DNA damage) in cell nuclei as a function of increasing LET of the traversing particles, reaching a quasi-plateau when the LET exceeded 80-90 keV.mu m(-1). For the LET of an alpha particle ranging from 80-90 to 170 keV.mu m(-1), 10-30% of the parti
机译:加速器技术的进展,它能够使符合带电的辐射物种的放射治疗,带来了患者的益处以及潜在的新风险。为了更好地了解电离辐射对肿瘤和周围组织的影响,重要的是研究和量化纳米级和初始生物事件的能量沉积之间的关系。蒙特卡罗轨道结构仿真代码提供了一种调查这种关系的强大工具;然而,他们的成功和可靠性取决于他们对他们受到挑战的专用生物数据的改善和发展。为此目的,允许(根据辐射质量根据辐射质量评估在进入离子和DNA之间的相互作用后DNA损伤的相对频率的微观放射部设施。原发性人体细胞暴露于三种不同能量的α颗粒,各自的线性能量转移(允许)在细胞的“中心位置”或质子(19 kev.mum(-1))处的约36,85或170kev.mu m(-1) 。使用免疫荧光观察到核心焦焦形成(53bp1 /γ-h2ax)的统计评估,并在大量的细胞核中进行了与颗粒遍历。调整了生物学结果,以考虑推动实验不确定性的因素,然后在使用与我们实验中使用的细胞相同的平均几何形状和DNA密度的细胞核的虚拟体阵体上的电离颗粒相互作用的GEANT4-DNA码建模进行攻击。r对于在Let超过80-90Kev.mum(-1)的情况下,对细胞核中的焦点(或模拟DNA损伤)的焦点(或模拟DNA损伤)的相对频率增加了细胞核中的焦点(或模拟DNA损伤)的相对频率增加。为了让α粒子从80-90到170 kev.mu m(-1),10-30%的parti

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