Search arXivSearch

arXiv · 2210.01564

Simulation of DNA damage using Geant4-DNA: an overview of the "molecularDNA" example application

Abstract

The scientific community shows a great interest in the study of DNA damage induction, DNA damage repair and the biological effects on cells and cellular systems after exposure to ionizing radiation. Several in-silico methods have been proposed so far to study these mechanisms using Monte Carlo simulations. This study outlines a Geant4-DNA example application, named "molecularDNA", publicly released in the 11.1 version of Geant4 (December 2022). It was developed for novice Geant4 users and requires only a basic understanding of scripting languages to get started. The example currently proposes two different DNA-scale geometries of biological targets, namely "cylinders", and the "human cell". This public version is based on a previous prototype and includes new features such as: the adoption of a new approach for the modeling of the chemical stage (IRT-sync), the use of the Standard DNA Damage (SDD) format to describe radiation-induced DNA damage and upgraded computational tools to estimate DNA damage response. Simulation data in terms of single strand break (SSB) and double strand break (DSB) yields were produced using each of these geometries. The results were compared to the literature, to validate the example, producing less than 5 % difference in all cases.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Konstantinos P. Chatzipapas, Ngoc Hoang Tran, Milos Dordevic, Sara Zivkovic, Sara Zein, Wook Geun Shin, Dousatsu Sakata, Nathanael Lampe, Jeremy M. C. Brown, Aleksandra Ristic-Fira, Ivan Petrovic, Ioanna Kyriakou, Dimitris Emfietzoglou, Susanna Guatelli, Sébastien Incerti. 2023-03-20. Simulation of DNA damage using Geant4-DNA: an overview of the "molecularDNA" example application. https://doi.org/10.1002/pro6.1186

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Prediction of biological radiation effects based on ionization clusters (nanodosimetry)

This article reviews approaches that link the formation of ionization clusters in nanometric volumes to radiobiological effectiveness. The corresponding models were developed as the field of nanodosimetry developed. Some address early biological radiation effects, such as DNA damage, while most aim to predict cell survival or inactivation. The models also differ in the nanodosimetric quantities considered, with many based on the probability distribution of ionization cluster formation in a single target. Some models account for the synergistic effects of pairs of ionization clusters formed in different targets. Several models feature macroscopic aggregation frameworks based on particle fluence, which are proposed for use in radiotherapy treatment planning, particularly in ion-beam radiotherapy. The models are presented here using harmonized terminology and notation for nanodosimetric quantities. An extension of the conceptual framework of nanodosimetry is also discussed. This extension transitions from a target-centered description to a track-centered description. It also introduces nanodosimetry-based analogs of dosimetric concepts, such as dose and linear energy transfer. This paper traces and summarizes the historical development of nanodosimetry-based biological effect models and discusses conceptual aspects of the models to reveal their underlying assumptions and the extent to which they are mechanistic or merely elucidate correlations. Eventually, an attempt is made to identify the key open questions in this field that still need to be addressed.

physics.med-ph

Contextual Cellular Growth (ConCeG) of neural cells for realistic grey matter tissue generation for diffusion MRI simulations

Accurate interpretation of diffusion magnetic resonance imaging (dMRI) signals in grey matter (GM) remains challenging due to the complex, heterogeneous, and densely packed cellular environment. Numerical phantoms provide a controlled framework for investigating the relationship between microstructure and diffusion signals, yet existing approaches often lack the morphological realism and multi-cellular organisation required to faithfully represent GM tissue. In this work, we introduce Contextual Cellular Growth (ConCeG), a generative framework for creating individual cells or constructing dense, three-dimensional, multi-cellular GM substrates informed by real neuronal and glial morphologies. The method combines topological neuron synthesis with a spatially constrained growth network, allowing for the controlled generation of heterogeneous cellular environments with realistic intra- and extracellular compartments. Synthetic cells are generated using morphological and topological characteristics derived from biological reconstructions. We validate the framework through comparisons of structural features with real cellular data, demonstrating strong agreement in branch order, length, angle, and tortuosity distributions. Power spectrum analysis further shows that both intracellular compartments reproduce the spatial correlations observed in biological tissue. Together, these results show ConCeG provides a biologically grounded framework for generating grey matter substrates suitable for large scale diffusion MRI simulation.

physics.med-ph

A wearable, stretchable radio-frequency coil for extremity imaging in low-field MRI systems

Purpose: To develop a wearable, stretchable radio-frequency (RF) coil that conforms to the extremities and improves the filling factor in low-field MRI. Methods: A stretchable solenoid RF coil was fabricated by stitching a sinusoidally arranged Litz-wire conductor onto an elastic textile. The coil was compared with four rigid coils, including two routinely used designs and two prototypes designed to isolate the effects of conductor material and stretchability. Performance was characterized through quality-factor, loading-factor, transmit-efficiency, and image-based signal-to-noise ratio (SNR) measurements. Phantom and in-vivo knee experiments for one volunteer were performed using two portable MRI systems operating at 3.53 and 3.04 MHz. Results: The electrical performance of the selected Litz wire decreased with increasing frequency, becoming a slight disadvantage at 3.53 MHz. Nevertheless, the stretchable coil provided the highest phantom SNR in both systems, exceeding that of the best-performing rigid coil by approximately 8 % at 3.53 MHz and 20 % at 3.04 MHz. In vivo, its global SNR was 5 % lower than that of the best rigid coil at 3.53 MHz and 19 % higher at 3.04 MHz. Compared with the larger rigid coil required when knee positioning is constrained, the corresponding SNR improvements were approximately 18 % and 80 %. Conclusion: Anatomical conformity can compensate for the frequency-dependent electrical limitations of Litz wire in stretchable low-field RF coils. The proposed design provided SNR comparable to or greater than the best rigid designs while facilitating coil placement in subjects for whom smaller rigid coils may be impractical.

physics.med-ph