Tumor angiogenesis and vascular patterning: a mathematical model

Detalhes bibliográficos
Autor(a) principal: Travasso, Rui D. M.
Data de Publicação: 2011
Outros Autores: Corvera Poiré, Eugenia, Castro, Mário, Rodríguez-Manzaneque, Juan Carlos, Hernández-Machado, A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Texto Completo: https://hdl.handle.net/10316/110051
https://doi.org/10.1371/journal.pone.0019989
Resumo: Understanding tumor induced angiogenesis is a challenging problem with important consequences for diagnosis and treatment of cancer. Recently, strong evidences suggest the dual role of endothelial cells on the migrating tips and on the proliferating body of blood vessels, in consonance with further events behind lumen formation and vascular patterning. In this paper we present a multi-scale phase-field model that combines the benefits of continuum physics description and the capability of tracking individual cells. The model allows us to discuss the role of the endothelial cells' chemotactic response and proliferation rate as key factors that tailor the neovascular network. Importantly, we also test the predictions of our theoretical model against relevant experimental approaches in mice that displayed distinctive vascular patterns. The model reproduces the in vivo patterns of newly formed vascular networks, providing quantitative and qualitative results for branch density and vessel diameter on the order of the ones measured experimentally in mouse retinas. Our results highlight the ability of mathematical models to suggest relevant hypotheses with respect to the role of different parameters in this process, hence underlining the necessary collaboration between mathematical modeling, in vivo imaging and molecular biology techniques to improve current diagnostic and therapeutic tools.
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spelling Tumor angiogenesis and vascular patterning: a mathematical modelAngiogenesis Inducing AgentsAnimalsCapillariesCell ProliferationChemotaxisDiffusionMiceNeoplasmsNeovascularization, PathologicModels, BiologicalOrganogenesisUnderstanding tumor induced angiogenesis is a challenging problem with important consequences for diagnosis and treatment of cancer. Recently, strong evidences suggest the dual role of endothelial cells on the migrating tips and on the proliferating body of blood vessels, in consonance with further events behind lumen formation and vascular patterning. In this paper we present a multi-scale phase-field model that combines the benefits of continuum physics description and the capability of tracking individual cells. The model allows us to discuss the role of the endothelial cells' chemotactic response and proliferation rate as key factors that tailor the neovascular network. Importantly, we also test the predictions of our theoretical model against relevant experimental approaches in mice that displayed distinctive vascular patterns. The model reproduces the in vivo patterns of newly formed vascular networks, providing quantitative and qualitative results for branch density and vessel diameter on the order of the ones measured experimentally in mouse retinas. Our results highlight the ability of mathematical models to suggest relevant hypotheses with respect to the role of different parameters in this process, hence underlining the necessary collaboration between mathematical modeling, in vivo imaging and molecular biology techniques to improve current diagnostic and therapeutic tools.This work was supported by Fundação para a Ciencia e Tecnologia (http://www.fct.mctes.pt), project PTDC/SAU-ENB/110354/2009; Fundação Calouste Gulbenkian (http://www.gulbenkian.pt/), Estımulo a Investigação Prize; CONACyT (http://www.conacyt.mx/), project 83149; Instituto de Salud Carlos III (http:// www.isciii.es/), project EMER07/055; Spanish Ministry of Science and Innovation (http://www.micinn.es/), projects FIS2009-12964-C05-02 and FIS2009-12964-C05- 03.Public Library of Science2011info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://hdl.handle.net/10316/110051https://hdl.handle.net/10316/110051https://doi.org/10.1371/journal.pone.0019989eng1932-6203Travasso, Rui D. M.Corvera Poiré, EugeniaCastro, MárioRodríguez-Manzaneque, Juan CarlosHernández-Machado, A.info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-09-18T09:54:21Zoai:estudogeral.uc.pt:10316/110051Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T06:01:43.010473Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Tumor angiogenesis and vascular patterning: a mathematical model
title Tumor angiogenesis and vascular patterning: a mathematical model
spellingShingle Tumor angiogenesis and vascular patterning: a mathematical model
Travasso, Rui D. M.
Angiogenesis Inducing Agents
Animals
Capillaries
Cell Proliferation
Chemotaxis
Diffusion
Mice
Neoplasms
Neovascularization, Pathologic
Models, Biological
Organogenesis
title_short Tumor angiogenesis and vascular patterning: a mathematical model
title_full Tumor angiogenesis and vascular patterning: a mathematical model
title_fullStr Tumor angiogenesis and vascular patterning: a mathematical model
title_full_unstemmed Tumor angiogenesis and vascular patterning: a mathematical model
title_sort Tumor angiogenesis and vascular patterning: a mathematical model
author Travasso, Rui D. M.
author_facet Travasso, Rui D. M.
Corvera Poiré, Eugenia
Castro, Mário
Rodríguez-Manzaneque, Juan Carlos
Hernández-Machado, A.
author_role author
author2 Corvera Poiré, Eugenia
Castro, Mário
Rodríguez-Manzaneque, Juan Carlos
Hernández-Machado, A.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Travasso, Rui D. M.
Corvera Poiré, Eugenia
Castro, Mário
Rodríguez-Manzaneque, Juan Carlos
Hernández-Machado, A.
dc.subject.por.fl_str_mv Angiogenesis Inducing Agents
Animals
Capillaries
Cell Proliferation
Chemotaxis
Diffusion
Mice
Neoplasms
Neovascularization, Pathologic
Models, Biological
Organogenesis
topic Angiogenesis Inducing Agents
Animals
Capillaries
Cell Proliferation
Chemotaxis
Diffusion
Mice
Neoplasms
Neovascularization, Pathologic
Models, Biological
Organogenesis
description Understanding tumor induced angiogenesis is a challenging problem with important consequences for diagnosis and treatment of cancer. Recently, strong evidences suggest the dual role of endothelial cells on the migrating tips and on the proliferating body of blood vessels, in consonance with further events behind lumen formation and vascular patterning. In this paper we present a multi-scale phase-field model that combines the benefits of continuum physics description and the capability of tracking individual cells. The model allows us to discuss the role of the endothelial cells' chemotactic response and proliferation rate as key factors that tailor the neovascular network. Importantly, we also test the predictions of our theoretical model against relevant experimental approaches in mice that displayed distinctive vascular patterns. The model reproduces the in vivo patterns of newly formed vascular networks, providing quantitative and qualitative results for branch density and vessel diameter on the order of the ones measured experimentally in mouse retinas. Our results highlight the ability of mathematical models to suggest relevant hypotheses with respect to the role of different parameters in this process, hence underlining the necessary collaboration between mathematical modeling, in vivo imaging and molecular biology techniques to improve current diagnostic and therapeutic tools.
publishDate 2011
dc.date.none.fl_str_mv 2011
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv https://hdl.handle.net/10316/110051
https://hdl.handle.net/10316/110051
https://doi.org/10.1371/journal.pone.0019989
url https://hdl.handle.net/10316/110051
https://doi.org/10.1371/journal.pone.0019989
dc.language.iso.fl_str_mv eng
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dc.publisher.none.fl_str_mv Public Library of Science
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