Sci-Sat AM: Brachy - 06: Monte carlo DNA damage simulations of kV cbct radiation

2012 ◽  
Vol 39 (7Part4) ◽  
pp. 4645-4646
Author(s):  
C Kirkby ◽  
E Ghasroddashti ◽  
Y Poirier ◽  
M Tambasco ◽  
RD Stewart
Keyword(s):  
RSC Advances ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 6845-6858 ◽  
Author(s):  
N. T. Henthorn ◽  
J. W. Warmenhoven ◽  
M. Sotiropoulos ◽  
A. H. Aitkenhead ◽  
E. A. K. Smith ◽  
...  

Relative Biological Effectiveness (RBE) is a controversial and important topic in proton therapy. This work uses Monte Carlo simulations of DNA damage for protons and photons to probe this phenomenon, providing a plausible mechanistic understanding.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Dousatsu Sakata ◽  
Oleg Belov ◽  
Marie-Claude Bordage ◽  
Dimitris Emfietzoglou ◽  
Susanna Guatelli ◽  
...  

AbstractIonising radiation induced DNA damage and subsequent biological responses to it depend on the radiation’s track-structure and its energy loss distribution pattern. To investigate the underlying biological mechanisms involved in such complex system, there is need of predicting biological response by integrated Monte Carlo (MC) simulations across physics, chemistry and biology. Hence, in this work, we have developed an application using the open source Geant4-DNA toolkit to propose a realistic “fully integrated” MC simulation to calculate both early DNA damage and subsequent biological responses with time. We had previously developed an application allowing simulations of radiation induced early DNA damage on a naked cell nucleus model. In the new version presented in this work, we have developed three additional important features: (1) modeling of a realistic cell geometry, (2) inclusion of a biological repair model, (3) refinement of DNA damage parameters for direct damage and indirect damage scoring. The simulation results are validated with experimental data in terms of Single Strand Break (SSB) yields for plasmid and Double Strand Break (DSB) yields for plasmid/human cell. In addition, the yields of indirect DSBs are compatible with the experimental scavengeable damage fraction. The simulation application also demonstrates agreement with experimental data of $$\gamma$$ γ -H2AX yields for gamma ray irradiation. Using this application, it is now possible to predict biological response along time through track-structure MC simulations.


1999 ◽  
Vol 38 (1) ◽  
pp. 31-38 ◽  
Author(s):  
H. Nikjoo ◽  
P. O'Neill ◽  
M. Terrissol ◽  
D. T. Goodhead

2014 ◽  
Vol 90 (5) ◽  
pp. 392-400 ◽  
Author(s):  
Ya-Yun Hsiao ◽  
Tzu-Hsiang Hung ◽  
Shu-Ju Tu ◽  
Chuan-Jong Tung

2016 ◽  
Vol 3 (3) ◽  
pp. 352-361 ◽  
Author(s):  
Chun He ◽  
◽  
James C.L. Chow

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Alexander P. Klapproth ◽  
Jan Schuemann ◽  
Stefan Stangl ◽  
Tianwu Xie ◽  
Wei Bo Li ◽  
...  

Abstract Background Gold nanoparticles (AuNPs) are considered as promising agents to increase the radiosensitivity of tumor cells. However, the biological mechanisms of radiation enhancement effects of AuNPs are still not well understood. We present a multi-scale Monte Carlo simulation framework within TOPAS-nBio to investigate the increase of DNA damage due to the presence of AuNPs in mouse tumor models. Methods A tumor was placed inside a voxel mouse model and irradiated with either 100-kVp or 200-kVp X-ray beams. Phase spaces were employed to transfer particles from the macroscopic (voxel) scale to the microscopic scale, which consists of a cell geometry including a detailed mouse DNA model. Radiosensitizing effects were calculated in the presence and absence of hybrid nanoparticles with a $$\text{Fe}_2\text{O}_3$$ Fe 2 O 3 core surrounded by a gold layer (AuFeNPs). To simulate DNA damage even for very small energy tracks, Geant4-DNA physics and chemistry models were used on microscopic scale. Results An AuFeNP-induced enhancement of both dose and DNA strand breaks has been established for different scenarios. Produced chemical radicals including hydroxyl molecules, which were assumed to be responsible for DNA damage through chemical reactions, were found to be significantly increased. We further observed a dependency of the results on the location of the cells within the tumor for 200-kVp X-ray beams. Conclusion Our multi-scale approach allows to study irradiation-induced physical and chemical effects on cells. We showed a potential increase in cell radiosensitization caused by relatively small concentrations of AuFeNPs. Our new methodology allows the individual adjustment of parameters in each simulation step and therefore can be used for other studies investigating the radiosensitizing effects of AuFeNPs or AuNPs in living cells.


2009 ◽  
Vol 36 (6Part16) ◽  
pp. 2634-2634
Author(s):  
M Lee ◽  
Y Hsiao ◽  
T Chao ◽  
S Tu

2013 ◽  
Vol 40 (6Part18) ◽  
pp. 319-319
Author(s):  
C Kirkby ◽  
E Ghasroddashti ◽  
Y Poirier ◽  
M Tambasco ◽  
R Stewart

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