Development of computational model for cell dose and DNA damage quantification of multicellular system

被引:10
|
作者
Liu, Ruirui [1 ,2 ]
Zhao, Tianyu [2 ]
Swat, Maciej H. [3 ]
Reynoso, Francisco J. [2 ]
Higley, Kathryn A. [1 ]
机构
[1] Oregon State Univ, Sch Nucl Sci & Engn, Corvallis, OR 97331 USA
[2] Washington Univ, Dept Radiat Oncol, Sch Med, St Louis, MO 63130 USA
[3] Indiana Univ, Biocomplex Inst, Bloomington, IN USA
关键词
Geant4; Geant4-DNA; multicellular model; cellular dose; DNA damage; computational model; Monte Carlo simulation; MONTE-CARLO-SIMULATION; TRACK-STRUCTURE; IONIZING-RADIATION; TUMOR SPHEROIDS; STRAND BREAKS; LIQUID WATER; GEANT4-DNA; IRRADIATION; INDUCTION; ALGORITHM;
D O I
10.1080/09553002.2019.1642537
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Purpose: The aim of this study is to build a computational model to investigate the cell dose and cell DNA damage distribution of a multicellular tissue system under the irradiation. Materials and methods: In this work, we developed a computational model for quantifying cell dose and double strand break (DSB) number in a multicellular system by simulating the radiation transport in 2D and 3D cell culture. The model was based on an open-source radiation transport package, Geant4 with Geant4-DNA physics. First, the computational multicellular system was created using a developed program, CelllMaker. Second, the radiation transport simulation for cells was conducted using Geant4 package with the Geant4-DNA physics to obtain the cellular dose and cellular DSB yield. Results: Using the method described in this work, it is possible to obtain the cellular dose and DNA damage simultaneously. The developed model provides a solution for quantifying the cellular dose and cellular DNA damage which are not easily determined in a radiobiological experiment. Conclusions: With limited validation data for the model, this preliminary study provides a roadmap for building a comprehensive toolkit for simulating cellular dose and DNA damage of multicellular tissue systems.
引用
收藏
页码:1484 / 1497
页数:14
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