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Treatment Analysis in a Cancer Stem Cell Context Using a Tumor Growth Model Based on Cellular Automata
Cancer can be viewed as an emergent behavior in terms of complex system theory and artificial life, Cellular Automata (CA) being the tool most used for studying and characterizing the emergent behavior. Different approaches with CA models were used to model cancer growth. The use of the abstract mod...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503350/ https://www.ncbi.nlm.nih.gov/pubmed/26176702 http://dx.doi.org/10.1371/journal.pone.0132306 |
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author | Monteagudo, Ángel Santos, José |
author_facet | Monteagudo, Ángel Santos, José |
author_sort | Monteagudo, Ángel |
collection | PubMed |
description | Cancer can be viewed as an emergent behavior in terms of complex system theory and artificial life, Cellular Automata (CA) being the tool most used for studying and characterizing the emergent behavior. Different approaches with CA models were used to model cancer growth. The use of the abstract model of acquired cancer hallmarks permits the direct modeling at cellular level, where a cellular automaton defines the mitotic and apoptotic behavior of cells, and allows for an analysis of different dynamics of the cellular system depending on the presence of the different hallmarks. A CA model based on the presence of hallmarks in the cells, which includes a simulation of the behavior of Cancer Stem Cells (CSC) and their implications for the resultant growth behavior of the multicellular system, was employed. This modeling of cancer growth, in the avascular phase, was employed to analyze the effect of cancer treatments in a cancer stem cell context. The model clearly explains why, after treatment against non-stem cancer cells, the regrowth capability of CSCs generates a faster regrowth of tumor behavior, and also shows that a continuous low-intensity treatment does not favor CSC proliferation and differentiation, thereby allowing an unproblematic control of future tumor regrowth. The analysis performed indicates that, contrary to the current attempts at CSC control, trying to make CSC proliferation more difficult is an important point to consider, especially in the immediate period after a standard treatment for controlling non-stem cancer cell proliferation. |
format | Online Article Text |
id | pubmed-4503350 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45033502015-07-17 Treatment Analysis in a Cancer Stem Cell Context Using a Tumor Growth Model Based on Cellular Automata Monteagudo, Ángel Santos, José PLoS One Research Article Cancer can be viewed as an emergent behavior in terms of complex system theory and artificial life, Cellular Automata (CA) being the tool most used for studying and characterizing the emergent behavior. Different approaches with CA models were used to model cancer growth. The use of the abstract model of acquired cancer hallmarks permits the direct modeling at cellular level, where a cellular automaton defines the mitotic and apoptotic behavior of cells, and allows for an analysis of different dynamics of the cellular system depending on the presence of the different hallmarks. A CA model based on the presence of hallmarks in the cells, which includes a simulation of the behavior of Cancer Stem Cells (CSC) and their implications for the resultant growth behavior of the multicellular system, was employed. This modeling of cancer growth, in the avascular phase, was employed to analyze the effect of cancer treatments in a cancer stem cell context. The model clearly explains why, after treatment against non-stem cancer cells, the regrowth capability of CSCs generates a faster regrowth of tumor behavior, and also shows that a continuous low-intensity treatment does not favor CSC proliferation and differentiation, thereby allowing an unproblematic control of future tumor regrowth. The analysis performed indicates that, contrary to the current attempts at CSC control, trying to make CSC proliferation more difficult is an important point to consider, especially in the immediate period after a standard treatment for controlling non-stem cancer cell proliferation. Public Library of Science 2015-07-15 /pmc/articles/PMC4503350/ /pubmed/26176702 http://dx.doi.org/10.1371/journal.pone.0132306 Text en © 2015 Monteagudo, Santos http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Monteagudo, Ángel Santos, José Treatment Analysis in a Cancer Stem Cell Context Using a Tumor Growth Model Based on Cellular Automata |
title | Treatment Analysis in a Cancer Stem Cell Context Using a Tumor Growth Model Based on Cellular Automata |
title_full | Treatment Analysis in a Cancer Stem Cell Context Using a Tumor Growth Model Based on Cellular Automata |
title_fullStr | Treatment Analysis in a Cancer Stem Cell Context Using a Tumor Growth Model Based on Cellular Automata |
title_full_unstemmed | Treatment Analysis in a Cancer Stem Cell Context Using a Tumor Growth Model Based on Cellular Automata |
title_short | Treatment Analysis in a Cancer Stem Cell Context Using a Tumor Growth Model Based on Cellular Automata |
title_sort | treatment analysis in a cancer stem cell context using a tumor growth model based on cellular automata |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503350/ https://www.ncbi.nlm.nih.gov/pubmed/26176702 http://dx.doi.org/10.1371/journal.pone.0132306 |
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