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Updated: May 15, 2026

Cell Cycle-specific Measurement of γH2AX and Apoptosis After Genotoxic Stress by Flow Cytometry
Published on: September 1, 2019
Efficient cell-by-cell simulation of DNA double strand breaks, chromosome aberrations, and cell survival for low- and
Anthony Lim1,2, Matthew Stephen Andriotty1, Alexander O'Dell1
1Nuclear and Radiological Engineering and Medical Physics Program, Georgia Institute of Technology, Atlanta, GA, United States of America.
Abstract:
The increasing sophistication of Monte Carlo (MC)-based simulations, such as TOPAS-nBio for radiation track structure and DNA damage, and MEDRAS-MC for subsequent DNA repair and cell survival, has ushered in an era ofin-silicosingle-cell radiobiology. However, these simulations remain computationally prohibitive. In this study, we introduce a novel method that significantly accelerates the integrated simulation process forin-silicosingle-cell radiobiology. Our approach centers on pre-calculating and constructing a single-particle-track (SPT) standard DNA damage (SDD) data library using TOPAS-nBio. Each SPT-SDD data entry in this library records the positions of various DNA damage types (e.g. base damage, single-strand breaks, and double-strand breaks) produced by a single particle track. The comprehensive library contains a large number of SPT-SDD data entries, covering a broad range of particle energies. This data library functions as a look-up table, allowing for rapid assembly of DNA damage data for any desired dose level. This is achieved by randomly fetching and superimposing many SPT-SDD data entries from the pre-calculated library. The resulting 'composite' SDD data file then serves as input for MEDRAS-MC to simulate and compute DNA damage outcomes, including chromosome aberrations and cell lethality for each individual cell. Furthermore, 'timestamps' can be added to the superimposed data to account for dose rate effects. This work presents the first integrated MC framework that bridges track-structure simulation (TOPAS-nBio) with mechanistic repair-misrepair modeling (MEDRAS-MC) to predict chromosome aberrations and cell lethality on a cell-by-cell basis. In this paper, we first describe this novel methodology and then apply it to compute radiation-induced outcomes for three previously reportedin vitroexperiments. These applications involve 280 kVpx-rays, protons, and alpha particles, covering a broad spectrum of linear energy transfer. Finally, we compare ourin silicoresults with experimental data and provide a detailed discussion of any observed discrepancies.
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