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PhysiBoSS 2.0: a sustainable integration of stochastic Boolean and agent-based modelling frameworks

In systems biology, mathematical models and simulations play a crucial role in understanding complex biological systems. Different modelling frameworks are employed depending on the nature and scales of the system under study. For instance, signalling and regulatory networks can be simulated using B...

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Autores principales: Ponce-de-Leon, Miguel, Montagud, Arnau, Noël, Vincent, Meert, Annika, Pradas, Gerard, Barillot, Emmanuel, Calzone, Laurence, Valencia, Alfonso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616087/
https://www.ncbi.nlm.nih.gov/pubmed/37903760
http://dx.doi.org/10.1038/s41540-023-00314-4
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author Ponce-de-Leon, Miguel
Montagud, Arnau
Noël, Vincent
Meert, Annika
Pradas, Gerard
Barillot, Emmanuel
Calzone, Laurence
Valencia, Alfonso
author_facet Ponce-de-Leon, Miguel
Montagud, Arnau
Noël, Vincent
Meert, Annika
Pradas, Gerard
Barillot, Emmanuel
Calzone, Laurence
Valencia, Alfonso
author_sort Ponce-de-Leon, Miguel
collection PubMed
description In systems biology, mathematical models and simulations play a crucial role in understanding complex biological systems. Different modelling frameworks are employed depending on the nature and scales of the system under study. For instance, signalling and regulatory networks can be simulated using Boolean modelling, whereas multicellular systems can be studied using agent-based modelling. Herein, we present PhysiBoSS 2.0, a hybrid agent-based modelling framework that allows simulating signalling and regulatory networks within individual cell agents. PhysiBoSS 2.0 is a redesign and reimplementation of PhysiBoSS 1.0 and was conceived as an add-on that expands the PhysiCell functionalities by enabling the simulation of intracellular cell signalling using MaBoSS while keeping a decoupled, maintainable and model-agnostic design. PhysiBoSS 2.0 also expands the set of functionalities offered to the users, including custom models and cell specifications, mechanistic submodels of substrate internalisation and detailed control over simulation parameters. Together with PhysiBoSS 2.0, we introduce PCTK, a Python package developed for handling and processing simulation outputs, and generating summary plots and 3D renders. PhysiBoSS 2.0 allows studying the interplay between the microenvironment, the signalling pathways that control cellular processes and population dynamics, suitable for modelling cancer. We show different approaches for integrating Boolean networks into multi-scale simulations using strategies to study the drug effects and synergies in models of cancer cell lines and validate them using experimental data. PhysiBoSS 2.0 is open-source and publicly available on GitHub with several repositories of accompanying interoperable tools.
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spelling pubmed-106160872023-11-01 PhysiBoSS 2.0: a sustainable integration of stochastic Boolean and agent-based modelling frameworks Ponce-de-Leon, Miguel Montagud, Arnau Noël, Vincent Meert, Annika Pradas, Gerard Barillot, Emmanuel Calzone, Laurence Valencia, Alfonso NPJ Syst Biol Appl Article In systems biology, mathematical models and simulations play a crucial role in understanding complex biological systems. Different modelling frameworks are employed depending on the nature and scales of the system under study. For instance, signalling and regulatory networks can be simulated using Boolean modelling, whereas multicellular systems can be studied using agent-based modelling. Herein, we present PhysiBoSS 2.0, a hybrid agent-based modelling framework that allows simulating signalling and regulatory networks within individual cell agents. PhysiBoSS 2.0 is a redesign and reimplementation of PhysiBoSS 1.0 and was conceived as an add-on that expands the PhysiCell functionalities by enabling the simulation of intracellular cell signalling using MaBoSS while keeping a decoupled, maintainable and model-agnostic design. PhysiBoSS 2.0 also expands the set of functionalities offered to the users, including custom models and cell specifications, mechanistic submodels of substrate internalisation and detailed control over simulation parameters. Together with PhysiBoSS 2.0, we introduce PCTK, a Python package developed for handling and processing simulation outputs, and generating summary plots and 3D renders. PhysiBoSS 2.0 allows studying the interplay between the microenvironment, the signalling pathways that control cellular processes and population dynamics, suitable for modelling cancer. We show different approaches for integrating Boolean networks into multi-scale simulations using strategies to study the drug effects and synergies in models of cancer cell lines and validate them using experimental data. PhysiBoSS 2.0 is open-source and publicly available on GitHub with several repositories of accompanying interoperable tools. Nature Publishing Group UK 2023-10-30 /pmc/articles/PMC10616087/ /pubmed/37903760 http://dx.doi.org/10.1038/s41540-023-00314-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ponce-de-Leon, Miguel
Montagud, Arnau
Noël, Vincent
Meert, Annika
Pradas, Gerard
Barillot, Emmanuel
Calzone, Laurence
Valencia, Alfonso
PhysiBoSS 2.0: a sustainable integration of stochastic Boolean and agent-based modelling frameworks
title PhysiBoSS 2.0: a sustainable integration of stochastic Boolean and agent-based modelling frameworks
title_full PhysiBoSS 2.0: a sustainable integration of stochastic Boolean and agent-based modelling frameworks
title_fullStr PhysiBoSS 2.0: a sustainable integration of stochastic Boolean and agent-based modelling frameworks
title_full_unstemmed PhysiBoSS 2.0: a sustainable integration of stochastic Boolean and agent-based modelling frameworks
title_short PhysiBoSS 2.0: a sustainable integration of stochastic Boolean and agent-based modelling frameworks
title_sort physiboss 2.0: a sustainable integration of stochastic boolean and agent-based modelling frameworks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10616087/
https://www.ncbi.nlm.nih.gov/pubmed/37903760
http://dx.doi.org/10.1038/s41540-023-00314-4
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