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MINAS TIRITH: a new tool for simulating radiation-induced DNA damage at the cell population level
Y Thibaut1, G Gonon1, J S Martinez1
1Institut de Radioprotection et de Sûreté Nucléaire (IRSN), PSE-SANTE/SDOS/LDRI, PSE-SANTE/SERAMED/LRAcc, PSE-SANTE/SDOS/LMDN, BP 17, F-92262 Fontenay-aux-Roses, France.
The MINAS TIRITH tool models radiation-induced DNA damage across cell populations, bridging the gap between experimental data and simulations. This approach offers faster computation and enables direct comparison of modeling with biological experiments.
Area of Science:
- Radiation biology
- Computational biophysics
- Medical physics
Background:
- Understanding radiation-induced DNA damage is crucial for radiobiology and radiation protection.
- Current modeling often uses Monte Carlo simulations for single cells, differing in scale from population-level experiments.
- Stochastic energy deposition leads to non-uniform dose distributions in cell populations, complicating direct comparisons.
Purpose of the Study:
- To introduce the MINAS TIRITH tool for modeling radiation-induced DNA damage at the cell population level.
- To enable direct comparison between computational modeling and biological experiments.
- To address the scale difference between single-cell simulations and population-based experiments.
Main Methods:
- Utilized precomputed microdosimetric parameters and DNA damage distributions from Geant4-DNA.
- Assigned specific energy (z) to individual cells within a population based on absorbed dose (Dabs).
- Modeled DNA damage events per cell based on assigned specific energy, incorporating stochasticity.
Main Results:
- Validated MINAS TIRITH against Geant4-DNA track structure code and a simulation chain.
- Demonstrated consistency in dose distribution across populations and DNA damage calculations.
- Confirmed the tool's ability to accurately represent radiation effects at the cellular level.
Conclusions:
- MINAS TIRITH provides a novel approach for calculating population-level radiation-induced DNA damage.
- The tool significantly reduces simulation time compared to track structure codes.
- Facilitates more direct and meaningful comparisons between computational models and experimental findings in radiobiology.
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