Tumor angiogenesis and vascular patterning: a mathematical model.

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...

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Main Authors: Rui D M Travasso, Eugenia Corvera Poiré, Mario Castro, Juan Carlos Rodríguez-Manzaneque, A Hernández-Machado
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3103509?pdf=render
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spelling doaj-9166193f25344c26b259a89236aeef9f2020-11-25T02:33:34ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0165e1998910.1371/journal.pone.0019989Tumor angiogenesis and vascular patterning: a mathematical model.Rui D M TravassoEugenia Corvera PoiréMario CastroJuan Carlos Rodríguez-ManzanequeA Hernández-MachadoUnderstanding 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.http://europepmc.org/articles/PMC3103509?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Rui D M Travasso
Eugenia Corvera Poiré
Mario Castro
Juan Carlos Rodríguez-Manzaneque
A Hernández-Machado
spellingShingle Rui D M Travasso
Eugenia Corvera Poiré
Mario Castro
Juan Carlos Rodríguez-Manzaneque
A Hernández-Machado
Tumor angiogenesis and vascular patterning: a mathematical model.
PLoS ONE
author_facet Rui D M Travasso
Eugenia Corvera Poiré
Mario Castro
Juan Carlos Rodríguez-Manzaneque
A Hernández-Machado
author_sort Rui D M Travasso
title Tumor angiogenesis and vascular patterning: a mathematical model.
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.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
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.
url http://europepmc.org/articles/PMC3103509?pdf=render
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