Nonlinear simulations of solid tumor growth using a mixture model: invasion and branching
We develop a thermodynamically consistent mixture model for avascular solid tumor growth which takes into account the effects of cell-to-cell adhesion, and taxis inducing chemical and molecular species. The mixture model is well-posed and the governing equations are of Cahn-Hilliard type. When there...
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description | We develop a thermodynamically consistent mixture model for avascular solid tumor growth which takes into account the effects of cell-to-cell adhesion, and taxis inducing chemical and molecular species. The mixture model is well-posed and the governing equations are of Cahn-Hilliard type. When there are only two phases, our asymptotic analysis shows that earlier single-phase models may be recovered as limiting cases of a two-phase model. To solve the governing equations, we develop a numerical algorithm based on an adaptive Cartesian block-structured mesh refinement scheme. A centered-difference approximation is used for the space discretization so that the scheme is second order accurate in space. An implicit discretization in time is used which results in nonlinear equations at implicit time levels. We further employ a gradient stable discretization scheme so that the nonlinear equations are solvable for very large time steps. To solve those equations we use a nonlinear multilevel/multigrid method which is of an optimal order O(N) where N is the number of grid points. Spherically symmetric and fully two dimensional nonlinear numerical simulations are performed. We investigate tumor evolution in nutrient-rich and nutrient-poor tissues. A number of important results have been uncovered. For example, we demonstrate that the tumor may suffer from taxis-driven fingering instabilities which are most dramatic when cell proliferation is low, as predicted by linear stability theory. This is also observed in experiments. This work shows that taxis may play a role in tumor invasion and that when nutrient plays the role of a chemoattractant, the diffusional instability is exacerbated by nutrient gradients. Accordingly, we believe this model is capable of describing complex invasive patterns observed in experiments. |
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The mixture model is well-posed and the governing equations are of Cahn-Hilliard type. When there are only two phases, our asymptotic analysis shows that earlier single-phase models may be recovered as limiting cases of a two-phase model. To solve the governing equations, we develop a numerical algorithm based on an adaptive Cartesian block-structured mesh refinement scheme. A centered-difference approximation is used for the space discretization so that the scheme is second order accurate in space. An implicit discretization in time is used which results in nonlinear equations at implicit time levels. We further employ a gradient stable discretization scheme so that the nonlinear equations are solvable for very large time steps. To solve those equations we use a nonlinear multilevel/multigrid method which is of an optimal order O(N) where N is the number of grid points. Spherically symmetric and fully two dimensional nonlinear numerical simulations are performed. We investigate tumor evolution in nutrient-rich and nutrient-poor tissues. A number of important results have been uncovered. For example, we demonstrate that the tumor may suffer from taxis-driven fingering instabilities which are most dramatic when cell proliferation is low, as predicted by linear stability theory. This is also observed in experiments. This work shows that taxis may play a role in tumor invasion and that when nutrient plays the role of a chemoattractant, the diffusional instability is exacerbated by nutrient gradients. Accordingly, we believe this model is capable of describing complex invasive patterns observed in experiments.</description><identifier>ISSN: 0303-6812</identifier><identifier>EISSN: 1432-1416</identifier><identifier>DOI: 10.1007/s00285-008-0215-x</identifier><identifier>PMID: 18787827</identifier><language>eng</language><publisher>Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag</publisher><subject>Adaptive mesh refinement ; Algorithms ; Animals ; Applications of Mathematics ; Body Water - physiology ; Cahn-Hilliard equation ; Cell Adhesion - physiology ; Cell Proliferation ; chemotaxis ; Humans ; Linear Models ; Mathematical and Computational Biology ; Mathematical Concepts ; Mathematics ; Mathematics and Statistics ; Mixture theory ; Models, Biological ; Neoplasm Invasiveness - pathology ; Neoplasm Invasiveness - physiopathology ; Neoplasms - pathology ; Neoplasms - physiopathology ; Nonlinear Dynamics ; Nonlinear multigrid methods ; Nonlinear simulation ; Solid tumor growth ; Spheroids, Cellular - pathology ; Thermodynamics ; Tumor Cells, Cultured</subject><ispartof>Journal of mathematical biology, 2009-04, Vol.58 (4-5), p.723-763</ispartof><rights>Springer-Verlag 2008</rights><rights>Springer-Verlag 2009</rights><rights>Springer-Verlag 2008 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c557t-278d5d888a547fe374c3f5cae91ab19e07f1a2ae548b15d86e5b7ef0736c248a3</citedby><cites>FETCH-LOGICAL-c557t-278d5d888a547fe374c3f5cae91ab19e07f1a2ae548b15d86e5b7ef0736c248a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00285-008-0215-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00285-008-0215-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18787827$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cristini, Vittorio</creatorcontrib><creatorcontrib>Li, Xiangrong</creatorcontrib><creatorcontrib>Lowengrub, John S</creatorcontrib><creatorcontrib>Wise, Steven M</creatorcontrib><title>Nonlinear simulations of solid tumor growth using a mixture model: invasion and branching</title><title>Journal of mathematical biology</title><addtitle>J. Math. Biol</addtitle><addtitle>J Math Biol</addtitle><description>We develop a thermodynamically consistent mixture model for avascular solid tumor growth which takes into account the effects of cell-to-cell adhesion, and taxis inducing chemical and molecular species. The mixture model is well-posed and the governing equations are of Cahn-Hilliard type. When there are only two phases, our asymptotic analysis shows that earlier single-phase models may be recovered as limiting cases of a two-phase model. To solve the governing equations, we develop a numerical algorithm based on an adaptive Cartesian block-structured mesh refinement scheme. A centered-difference approximation is used for the space discretization so that the scheme is second order accurate in space. An implicit discretization in time is used which results in nonlinear equations at implicit time levels. We further employ a gradient stable discretization scheme so that the nonlinear equations are solvable for very large time steps. To solve those equations we use a nonlinear multilevel/multigrid method which is of an optimal order O(N) where N is the number of grid points. Spherically symmetric and fully two dimensional nonlinear numerical simulations are performed. We investigate tumor evolution in nutrient-rich and nutrient-poor tissues. A number of important results have been uncovered. For example, we demonstrate that the tumor may suffer from taxis-driven fingering instabilities which are most dramatic when cell proliferation is low, as predicted by linear stability theory. This is also observed in experiments. This work shows that taxis may play a role in tumor invasion and that when nutrient plays the role of a chemoattractant, the diffusional instability is exacerbated by nutrient gradients. Accordingly, we believe this model is capable of describing complex invasive patterns observed in experiments.</description><subject>Adaptive mesh refinement</subject><subject>Algorithms</subject><subject>Animals</subject><subject>Applications of Mathematics</subject><subject>Body Water - physiology</subject><subject>Cahn-Hilliard equation</subject><subject>Cell Adhesion - physiology</subject><subject>Cell Proliferation</subject><subject>chemotaxis</subject><subject>Humans</subject><subject>Linear Models</subject><subject>Mathematical and Computational Biology</subject><subject>Mathematical Concepts</subject><subject>Mathematics</subject><subject>Mathematics and Statistics</subject><subject>Mixture theory</subject><subject>Models, Biological</subject><subject>Neoplasm Invasiveness - pathology</subject><subject>Neoplasm Invasiveness - physiopathology</subject><subject>Neoplasms - pathology</subject><subject>Neoplasms - physiopathology</subject><subject>Nonlinear Dynamics</subject><subject>Nonlinear multigrid methods</subject><subject>Nonlinear simulation</subject><subject>Solid tumor growth</subject><subject>Spheroids, Cellular - 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physiology</topic><topic>Cahn-Hilliard equation</topic><topic>Cell Adhesion - physiology</topic><topic>Cell Proliferation</topic><topic>chemotaxis</topic><topic>Humans</topic><topic>Linear Models</topic><topic>Mathematical and Computational Biology</topic><topic>Mathematical Concepts</topic><topic>Mathematics</topic><topic>Mathematics and Statistics</topic><topic>Mixture theory</topic><topic>Models, Biological</topic><topic>Neoplasm Invasiveness - pathology</topic><topic>Neoplasm Invasiveness - physiopathology</topic><topic>Neoplasms - pathology</topic><topic>Neoplasms - physiopathology</topic><topic>Nonlinear Dynamics</topic><topic>Nonlinear multigrid methods</topic><topic>Nonlinear simulation</topic><topic>Solid tumor growth</topic><topic>Spheroids, Cellular - pathology</topic><topic>Thermodynamics</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cristini, Vittorio</creatorcontrib><creatorcontrib>Li, Xiangrong</creatorcontrib><creatorcontrib>Lowengrub, John S</creatorcontrib><creatorcontrib>Wise, Steven M</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Computer Science Collection</collection><collection>Computer Science Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of mathematical biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cristini, Vittorio</au><au>Li, Xiangrong</au><au>Lowengrub, John S</au><au>Wise, Steven M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nonlinear simulations of solid tumor growth using a mixture model: invasion and branching</atitle><jtitle>Journal of mathematical biology</jtitle><stitle>J. Math. Biol</stitle><addtitle>J Math Biol</addtitle><date>2009-04-01</date><risdate>2009</risdate><volume>58</volume><issue>4-5</issue><spage>723</spage><epage>763</epage><pages>723-763</pages><issn>0303-6812</issn><eissn>1432-1416</eissn><abstract>We develop a thermodynamically consistent mixture model for avascular solid tumor growth which takes into account the effects of cell-to-cell adhesion, and taxis inducing chemical and molecular species. The mixture model is well-posed and the governing equations are of Cahn-Hilliard type. When there are only two phases, our asymptotic analysis shows that earlier single-phase models may be recovered as limiting cases of a two-phase model. To solve the governing equations, we develop a numerical algorithm based on an adaptive Cartesian block-structured mesh refinement scheme. A centered-difference approximation is used for the space discretization so that the scheme is second order accurate in space. An implicit discretization in time is used which results in nonlinear equations at implicit time levels. We further employ a gradient stable discretization scheme so that the nonlinear equations are solvable for very large time steps. To solve those equations we use a nonlinear multilevel/multigrid method which is of an optimal order O(N) where N is the number of grid points. Spherically symmetric and fully two dimensional nonlinear numerical simulations are performed. We investigate tumor evolution in nutrient-rich and nutrient-poor tissues. A number of important results have been uncovered. For example, we demonstrate that the tumor may suffer from taxis-driven fingering instabilities which are most dramatic when cell proliferation is low, as predicted by linear stability theory. This is also observed in experiments. This work shows that taxis may play a role in tumor invasion and that when nutrient plays the role of a chemoattractant, the diffusional instability is exacerbated by nutrient gradients. Accordingly, we believe this model is capable of describing complex invasive patterns observed in experiments.</abstract><cop>Berlin/Heidelberg</cop><pub>Berlin/Heidelberg : Springer-Verlag</pub><pmid>18787827</pmid><doi>10.1007/s00285-008-0215-x</doi><tpages>41</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adaptive mesh refinement Algorithms Animals Applications of Mathematics Body Water - physiology Cahn-Hilliard equation Cell Adhesion - physiology Cell Proliferation chemotaxis Humans Linear Models Mathematical and Computational Biology Mathematical Concepts Mathematics Mathematics and Statistics Mixture theory Models, Biological Neoplasm Invasiveness - pathology Neoplasm Invasiveness - physiopathology Neoplasms - pathology Neoplasms - physiopathology Nonlinear Dynamics Nonlinear multigrid methods Nonlinear simulation Solid tumor growth Spheroids, Cellular - pathology Thermodynamics Tumor Cells, Cultured |
title | Nonlinear simulations of solid tumor growth using a mixture model: invasion and branching |
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