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The complexity of DNA damage by radiation follows a Gamma distribution: insights from the Microdosimetric Gamma Model
INTRODUCTION: DNA damage is the main predictor of response to radiation therapy for cancer. Its Q8 quantification and characterization are paramount for treatment optimization, particularly in advanced modalities such as proton and alpha-targeted therapy. METHODS: We present a novel approach called...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313124/ https://www.ncbi.nlm.nih.gov/pubmed/37397382 http://dx.doi.org/10.3389/fonc.2023.1196502 |
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author | Bertolet, Alejandro Chamseddine, Ibrahim Paganetti, Harald Schuemann, Jan |
author_facet | Bertolet, Alejandro Chamseddine, Ibrahim Paganetti, Harald Schuemann, Jan |
author_sort | Bertolet, Alejandro |
collection | PubMed |
description | INTRODUCTION: DNA damage is the main predictor of response to radiation therapy for cancer. Its Q8 quantification and characterization are paramount for treatment optimization, particularly in advanced modalities such as proton and alpha-targeted therapy. METHODS: We present a novel approach called the Microdosimetric Gamma Model (MGM) to address this important issue. The MGM uses the theory of microdosimetry, specifically the mean energy imparted to small sites, as a predictor of DNA damage properties. MGM provides the number of DNA damage sites and their complexity, which were determined using Monte Carlo simulations with the TOPAS-nBio toolkit for monoenergetic protons and alpha particles. Complexity was used together with a illustrative and simplistic repair model to depict the differences between high and low LET radiations. RESULTS: DNA damage complexity distributions were were found to follow a Gamma distribution for all monoenergetic particles studied. The MGM functions allowed to predict number of DNA damage sites and their complexity for particles not simulated with microdosimetric measurements (yF) in the range of those studied. DISCUSSION: Compared to current methods, MGM allows for the characterization of DNA damage induced by beams composed of multi-energy components distributed over any time configuration and spatial distribution. The output can be plugged into ad hoc repair models that can predict cell killing, protein recruitment at repair sites, chromosome aberrations, and other biological effects, as opposed to current models solely focusing on cell survival. These features are particularly important in targeted alpha-therapy, for which biological effects remain largely uncertain. The MGM provides a flexible framework to study the energy, time, and spatial aspects of ionizing radiation and offers an excellent tool for studying and optimizing the biological effects of these radiotherapy modalities. |
format | Online Article Text |
id | pubmed-10313124 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103131242023-07-01 The complexity of DNA damage by radiation follows a Gamma distribution: insights from the Microdosimetric Gamma Model Bertolet, Alejandro Chamseddine, Ibrahim Paganetti, Harald Schuemann, Jan Front Oncol Oncology INTRODUCTION: DNA damage is the main predictor of response to radiation therapy for cancer. Its Q8 quantification and characterization are paramount for treatment optimization, particularly in advanced modalities such as proton and alpha-targeted therapy. METHODS: We present a novel approach called the Microdosimetric Gamma Model (MGM) to address this important issue. The MGM uses the theory of microdosimetry, specifically the mean energy imparted to small sites, as a predictor of DNA damage properties. MGM provides the number of DNA damage sites and their complexity, which were determined using Monte Carlo simulations with the TOPAS-nBio toolkit for monoenergetic protons and alpha particles. Complexity was used together with a illustrative and simplistic repair model to depict the differences between high and low LET radiations. RESULTS: DNA damage complexity distributions were were found to follow a Gamma distribution for all monoenergetic particles studied. The MGM functions allowed to predict number of DNA damage sites and their complexity for particles not simulated with microdosimetric measurements (yF) in the range of those studied. DISCUSSION: Compared to current methods, MGM allows for the characterization of DNA damage induced by beams composed of multi-energy components distributed over any time configuration and spatial distribution. The output can be plugged into ad hoc repair models that can predict cell killing, protein recruitment at repair sites, chromosome aberrations, and other biological effects, as opposed to current models solely focusing on cell survival. These features are particularly important in targeted alpha-therapy, for which biological effects remain largely uncertain. The MGM provides a flexible framework to study the energy, time, and spatial aspects of ionizing radiation and offers an excellent tool for studying and optimizing the biological effects of these radiotherapy modalities. Frontiers Media S.A. 2023-06-16 /pmc/articles/PMC10313124/ /pubmed/37397382 http://dx.doi.org/10.3389/fonc.2023.1196502 Text en Copyright © 2023 Bertolet, Chamseddine, Paganetti and Schuemann https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Bertolet, Alejandro Chamseddine, Ibrahim Paganetti, Harald Schuemann, Jan The complexity of DNA damage by radiation follows a Gamma distribution: insights from the Microdosimetric Gamma Model |
title | The complexity of DNA damage by radiation follows a Gamma distribution: insights from the Microdosimetric Gamma Model |
title_full | The complexity of DNA damage by radiation follows a Gamma distribution: insights from the Microdosimetric Gamma Model |
title_fullStr | The complexity of DNA damage by radiation follows a Gamma distribution: insights from the Microdosimetric Gamma Model |
title_full_unstemmed | The complexity of DNA damage by radiation follows a Gamma distribution: insights from the Microdosimetric Gamma Model |
title_short | The complexity of DNA damage by radiation follows a Gamma distribution: insights from the Microdosimetric Gamma Model |
title_sort | complexity of dna damage by radiation follows a gamma distribution: insights from the microdosimetric gamma model |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313124/ https://www.ncbi.nlm.nih.gov/pubmed/37397382 http://dx.doi.org/10.3389/fonc.2023.1196502 |
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