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Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis
BACKGROUND: We investigated an algorithmic approach to modelling angiogenesis controlled by vascular endothelial growth factor (VEGF), the anti-angiogenic soluble VEGF receptor 1 (sVEGFR-1) and adenosine (Ado). We explored its feasibility to test angiogenesis-relevant hypotheses. We illustrated its...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090359/ https://www.ncbi.nlm.nih.gov/pubmed/21477269 http://dx.doi.org/10.1186/1742-4682-8-7 |
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author | Azuaje, Francisco Léonard, Frédérique Rolland-Turner, Magali Devaux, Yvan Wagner, Daniel R |
author_facet | Azuaje, Francisco Léonard, Frédérique Rolland-Turner, Magali Devaux, Yvan Wagner, Daniel R |
author_sort | Azuaje, Francisco |
collection | PubMed |
description | BACKGROUND: We investigated an algorithmic approach to modelling angiogenesis controlled by vascular endothelial growth factor (VEGF), the anti-angiogenic soluble VEGF receptor 1 (sVEGFR-1) and adenosine (Ado). We explored its feasibility to test angiogenesis-relevant hypotheses. We illustrated its potential to investigate the role of Ado as an angiogenesis modulator by enhancing VEGF activity and antagonizing sVEGFR-1. RESULTS: We implemented an algorithmic model of angiogenesis consisting of the dynamic interaction of endothelial cells, VEGF, sVEGFR-1 and Ado entities. The model is based on a logic rule-based methodology in which the local behaviour of the cells and molecules is encoded using if-then rules. The model shows how Ado may enhance angiogenesis through activating and inhibiting effects on VEGF and sVEGFR-1 respectively. Despite the relative simplicity of the model, it recapitulated basic features observed in in vitro models. However, observed disagreements between our models and in vitro data suggest possible knowledge gaps and may guide future experimental directions. CONCLUSIONS: The proposed model can support the exploration of hypotheses about the role of different molecular entities and experimental conditions in angiogenesis. Future expansions can also be applied to assist research planning in this and other biomedical domains. |
format | Text |
id | pubmed-3090359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30903592011-05-10 Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis Azuaje, Francisco Léonard, Frédérique Rolland-Turner, Magali Devaux, Yvan Wagner, Daniel R Theor Biol Med Model Research BACKGROUND: We investigated an algorithmic approach to modelling angiogenesis controlled by vascular endothelial growth factor (VEGF), the anti-angiogenic soluble VEGF receptor 1 (sVEGFR-1) and adenosine (Ado). We explored its feasibility to test angiogenesis-relevant hypotheses. We illustrated its potential to investigate the role of Ado as an angiogenesis modulator by enhancing VEGF activity and antagonizing sVEGFR-1. RESULTS: We implemented an algorithmic model of angiogenesis consisting of the dynamic interaction of endothelial cells, VEGF, sVEGFR-1 and Ado entities. The model is based on a logic rule-based methodology in which the local behaviour of the cells and molecules is encoded using if-then rules. The model shows how Ado may enhance angiogenesis through activating and inhibiting effects on VEGF and sVEGFR-1 respectively. Despite the relative simplicity of the model, it recapitulated basic features observed in in vitro models. However, observed disagreements between our models and in vitro data suggest possible knowledge gaps and may guide future experimental directions. CONCLUSIONS: The proposed model can support the exploration of hypotheses about the role of different molecular entities and experimental conditions in angiogenesis. Future expansions can also be applied to assist research planning in this and other biomedical domains. BioMed Central 2011-04-08 /pmc/articles/PMC3090359/ /pubmed/21477269 http://dx.doi.org/10.1186/1742-4682-8-7 Text en Copyright ©2011 Azuaje et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Azuaje, Francisco Léonard, Frédérique Rolland-Turner, Magali Devaux, Yvan Wagner, Daniel R Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis |
title | Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis |
title_full | Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis |
title_fullStr | Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis |
title_full_unstemmed | Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis |
title_short | Proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis |
title_sort | proof-of-principle investigation of an algorithmic model of adenosine-mediated angiogenesis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090359/ https://www.ncbi.nlm.nih.gov/pubmed/21477269 http://dx.doi.org/10.1186/1742-4682-8-7 |
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