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用不同 LET 的粒子束模拟染色体畸变响应函数。

Modeling of chromosome aberration response functions induced by particle beams with different LET.

机构信息

Institute of Physics, University of Szczecin, ul. Wielkopolska 15, 70-451, Szczecin, Poland.

Faculty of Marine Engineering, Maritime University of Szczecin, Wały Chrobrego 1-2, 70-500, Szczecin, Poland.

出版信息

Radiat Environ Biophys. 2020 Mar;59(1):79-87. doi: 10.1007/s00411-019-00822-0. Epub 2019 Nov 21.

DOI:10.1007/s00411-019-00822-0
PMID:31754773
Abstract

This study is based on our already published experimental data (Kowalska et al. in Radiat Environ Biophys 58:99-108, 2019) and is devoted to modeling of chromosome aberrations in human lymphocytes induced by 22.1 MeV/u B ions, 199 MeV/u C ions, 150 MeV and spread-out Bragg peak (SOBP) proton beams as well as by Co γ rays. The curvature of the dose-effect curves determined by the linear-quadratic model was considered in the frame of a simple analytical approach taking into account increase in the irradiation dose due to overlapping interaction regions of ion tracks. The model enabled to estimate effective interaction radius which could be compared with the physical expectations. The results were also compared to the Amorphous Track Structure Model of Katz which allows to get some additional information about the ion track structure. The analysis showed that the curvature of the experimental dose-effect curves mainly results from highly efficient repair processes of the DNA damage.

摘要

本研究基于我们已发表的实验数据(Kowalska 等人,Radiat Environ Biophys 58:99-108, 2019),致力于模拟 22.1 MeV/u B 离子、199 MeV/u C 离子、150 MeV 和扩展布拉格峰(SOBP)质子束以及 Co γ 射线诱导的人淋巴细胞染色体畸变。在线性二次模型确定的剂量-效应曲线的曲率,考虑到由于离子轨迹重叠相互作用区域而增加的照射剂量,在简单的分析方法的框架内进行了考虑。该模型能够估计有效相互作用半径,可与物理预期进行比较。结果还与 Katz 的无定形轨迹结构模型进行了比较,该模型可以提供有关离子轨迹结构的一些附加信息。分析表明,实验剂量-效应曲线的曲率主要是由于 DNA 损伤的高效修复过程。

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本文引用的文献

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Radiat Environ Biophys. 2019 Mar;58(1):99-108. doi: 10.1007/s00411-018-0771-4. Epub 2019 Jan 17.
2
Proximity effects in chromosome aberration induction: Dependence on radiation quality, cell type and dose.染色体畸变诱发的近程效应:依赖于辐射质量、细胞类型和剂量。
DNA Repair (Amst). 2018 Apr;64:45-52. doi: 10.1016/j.dnarep.2018.02.006. Epub 2018 Feb 22.
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Comprehensive track-structure based evaluation of DNA damage by light ions from radiotherapy-relevant energies down to stopping.
基于综合径迹结构的从放射治疗相关能量直至停止能量的轻离子致 DNA 损伤评估。
Sci Rep. 2017 Mar 27;7:45161. doi: 10.1038/srep45161.
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Dependence and independence of survival parameters on linear energy transfer in cells and tissues.细胞和组织中生存参数对线性能量传递的依赖性和独立性。
J Radiat Res. 2016 Nov;57(6):596-606. doi: 10.1093/jrr/rrw058. Epub 2016 Jul 5.
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Biological Effectiveness of Accelerated Protons for Chromosome Exchanges.加速质子对染色体交换的生物学效应
Front Oncol. 2015 Oct 19;5:226. doi: 10.3389/fonc.2015.00226. eCollection 2015.
6
The BIANCA model/code of radiation-induced cell death: application to human cells exposed to different radiation types.辐射诱导细胞死亡的BIANCA模型/代码:应用于暴露于不同辐射类型的人类细胞。
Radiat Environ Biophys. 2014 Aug;53(3):525-33. doi: 10.1007/s00411-014-0537-6.
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Track structure based modelling of chromosome aberrations after photon and alpha-particle irradiation.基于径迹结构的光子和 α 粒子辐照后染色体畸变建模。
Mutat Res. 2013 Aug 30;756(1-2):213-23. doi: 10.1016/j.mrgentox.2013.06.013. Epub 2013 Jun 28.
8
Chromosome damage in human cells by γ rays, α particles and heavy ions: track interactions in basic dose-response relationships.γ 射线、α 粒子和重离子对人类细胞的染色体损伤:基础剂量-反应关系中的轨迹相互作用。
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9
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Int J Radiat Biol. 2012 Jan;88(1-2):103-7. doi: 10.3109/09553002.2011.611213. Epub 2011 Oct 5.
10
Chromosome aberration measurements in mitotic and G2-PCC lymphocytes at the standard sampling time of 48 h underestimate the effectiveness of high-LET particles.在48小时的标准采样时间对有丝分裂期和G2-PCC淋巴细胞进行染色体畸变测量,会低估高传能线密度粒子的有效性。
Radiat Environ Biophys. 2011 Aug;50(3):371-81. doi: 10.1007/s00411-011-0360-2. Epub 2011 Apr 11.