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Multiscale biphasic modelling of peritumoural collagen microstructure: The effect of tumour growth on permeability and fluid flow
We present an in-silico model of avascular poroelastic tumour growth coupled with a multiscale biphasic description of the tumour–host environment. The model is specified to in-vitro data, facilitating biophysically realistic simulations of tumour spheroid growth into a dense collagen hydrogel. We u...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597211/ https://www.ncbi.nlm.nih.gov/pubmed/28902902 http://dx.doi.org/10.1371/journal.pone.0184511 |
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author | Wijeratne, Peter A. Hipwell, John H. Hawkes, David J. Stylianopoulos, Triantafyllos Vavourakis, Vasileios |
author_facet | Wijeratne, Peter A. Hipwell, John H. Hawkes, David J. Stylianopoulos, Triantafyllos Vavourakis, Vasileios |
author_sort | Wijeratne, Peter A. |
collection | PubMed |
description | We present an in-silico model of avascular poroelastic tumour growth coupled with a multiscale biphasic description of the tumour–host environment. The model is specified to in-vitro data, facilitating biophysically realistic simulations of tumour spheroid growth into a dense collagen hydrogel. We use the model to first confirm that passive mechanical remodelling of collagen fibres at the tumour boundary is driven by solid stress, and not fluid pressure. The model is then used to demonstrate the influence of collagen microstructure on peritumoural permeability and interstitial fluid flow. Our model suggests that at the tumour periphery, remodelling causes the peritumoural stroma to become more permeable in the circumferential than radial direction, and the interstitial fluid velocity is found to be dependent on initial collagen alignment. Finally we show that solid stresses are negatively correlated with peritumoural permeability, and positively correlated with interstitial fluid velocity. These results point to a heterogeneous, microstructure-dependent force environment at the tumour–peritumoural stroma interface. |
format | Online Article Text |
id | pubmed-5597211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55972112017-09-15 Multiscale biphasic modelling of peritumoural collagen microstructure: The effect of tumour growth on permeability and fluid flow Wijeratne, Peter A. Hipwell, John H. Hawkes, David J. Stylianopoulos, Triantafyllos Vavourakis, Vasileios PLoS One Research Article We present an in-silico model of avascular poroelastic tumour growth coupled with a multiscale biphasic description of the tumour–host environment. The model is specified to in-vitro data, facilitating biophysically realistic simulations of tumour spheroid growth into a dense collagen hydrogel. We use the model to first confirm that passive mechanical remodelling of collagen fibres at the tumour boundary is driven by solid stress, and not fluid pressure. The model is then used to demonstrate the influence of collagen microstructure on peritumoural permeability and interstitial fluid flow. Our model suggests that at the tumour periphery, remodelling causes the peritumoural stroma to become more permeable in the circumferential than radial direction, and the interstitial fluid velocity is found to be dependent on initial collagen alignment. Finally we show that solid stresses are negatively correlated with peritumoural permeability, and positively correlated with interstitial fluid velocity. These results point to a heterogeneous, microstructure-dependent force environment at the tumour–peritumoural stroma interface. Public Library of Science 2017-09-13 /pmc/articles/PMC5597211/ /pubmed/28902902 http://dx.doi.org/10.1371/journal.pone.0184511 Text en © 2017 Wijeratne et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wijeratne, Peter A. Hipwell, John H. Hawkes, David J. Stylianopoulos, Triantafyllos Vavourakis, Vasileios Multiscale biphasic modelling of peritumoural collagen microstructure: The effect of tumour growth on permeability and fluid flow |
title | Multiscale biphasic modelling of peritumoural collagen microstructure: The effect of tumour growth on permeability and fluid flow |
title_full | Multiscale biphasic modelling of peritumoural collagen microstructure: The effect of tumour growth on permeability and fluid flow |
title_fullStr | Multiscale biphasic modelling of peritumoural collagen microstructure: The effect of tumour growth on permeability and fluid flow |
title_full_unstemmed | Multiscale biphasic modelling of peritumoural collagen microstructure: The effect of tumour growth on permeability and fluid flow |
title_short | Multiscale biphasic modelling of peritumoural collagen microstructure: The effect of tumour growth on permeability and fluid flow |
title_sort | multiscale biphasic modelling of peritumoural collagen microstructure: the effect of tumour growth on permeability and fluid flow |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597211/ https://www.ncbi.nlm.nih.gov/pubmed/28902902 http://dx.doi.org/10.1371/journal.pone.0184511 |
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