Boundedness in a three-dimensional chemotaxis-haptotaxis model

DOI10.1007/S00033-015-0601-3MaRDI QIDQ286427zbMATH OpenOpenAlexFDO

Authors Xinru Cao

Publication date 20 May 2016

Published in ZAMP. Zeitschrift für angewandte Mathematik und Physik (Search for Journal in Brave)

Full work available at URL https://arxiv.org/abs/1501.05383

zbMATH Keywords

boundednesschemotaxislogistic sourcehaptotaxis

Mathematics Subject Classification ID

Stability in context of PDEs (35B35) Asymptotic behavior of solutions to PDEs (35B40) Reaction-diffusion equations (35K57) PDEs in connection with biology, chemistry and other natural sciences (35Q92) Cell movement (chemotaxis, etc.) (92C17)

Abstract: This paper studies the chemotaxis-haptotaxis system �egin{equation}

onumber left{ �egin{array}{llc} u_t=Delta u-chi ablacdot(u abla v)-xi ablacdot(u

abla w)+mu u(1-u-w), &(x,t)in Omega imes (0,T),\ v_t=Delta v-v+u, &(x,t)inOmega imes (0,T),\ w_t=-vw,&(x,t)in Omega imes (0,T) end{array} ight.quadquad(star) end{equation} under Neumann boundary conditions. Here $Omegasubsetmathbb{R}^3$ is a bounded domain with smooth boundary and the parameters $xi,chi,mu>0$. We prove that for nonnegative and suitably smooth initial data $(u_0,v_0,w_0)$, if $chi/mu$ is sufficiently small, ($star$) possesses a global classical solution which is bounded in $Omegaimes(0,infty)$. We underline that the result fully parallels the corresponding parabolic-elliptic-ODE system.

Recommendations

• Boundedness in a three-dimensional chemotaxis-haptotaxis model with nonlinear diffusion
• Global boundedness in a three-dimensional chemotaxis-haptotaxis model
• Global boundedness to a chemotaxis-haptotaxis model with nonlinear diffusion
• Global boundedness in a chemotaxis-haptotaxis model with nonlinear diffusion and signal production
• Boundedness in a multi-dimensional chemotaxis-haptotaxis model with nonlinear diffusion

Cites work

• scientific article; zbMATH DE number 1133142 (Why is no real title available?)
• A Chemotaxis System with Logistic Source
• A user's guide to PDE models for chemotaxis
• Aggregation vs. global diffusive behavior in the higher-dimensional Keller-Segel model
• Boundedness and stabilization in a multi-dimensional chemotaxis-haptotaxis model
• Boundedness in the Higher-Dimensional Parabolic-Parabolic Chemotaxis System with Logistic Source
• Boundedness vs. blow-up in a chemotaxis system
• Dominance of chemotaxis in a chemotaxis-haptotaxis model
• Energy-type estimates and global solvability in a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant
• Exponential attractor for a chemotaxis-growth system of equations
• Finite-time blow-up in the higher-dimensional parabolic-parabolic Keller-Segel system
• From 1970 until present: The Keller-Segel model in chemotaxis and its consequences. I
• Global existence for a haptotaxis model of cancer invasion with tissue remodeling
• Global solution for a chemotactic–haptotactic model of cancer invasion
• Global weak solutions in a PDE-ODE system modeling multiscale cancer cell invasion
• Heat kernels and maximal l^p—l^qestimates for parabolic evolution equations
• Initiation of slime mold aggregation viewed as an instability
• L^PBounds of solutions of reaction-diffusion equations
• Mathematical modelling of cancer invasion of tissue: dynamic heterogeneity
• Toward a mathematical theory of Keller-Segel models of pattern formation in biological tissues

Cited in

(84)

• A quasilinear chemotaxis-haptotaxis model: the roles of nonlinear diffusion and logistic source
• Boundedness in a two-dimensional two-species cancer invasion haptotaxis model without cell proliferation
• BOUNDEDNESS OF SOLUTIONS OF A HAPTOTAXIS MODEL
• Global boundedness in an oncolytic virotherapy model with generalized logistic source
• Boundedness in a quasilinear chemotaxis-haptotaxis model of parabolic-parabolic-ODE type
• Global attractors in a two-species chemotaxis system with two chemicals and variable logistic sources
• A note for global existence of a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant
• Mathematical research for models which is related to chemotaxis system
• Finite-time blow-up in low-dimensional Keller-Segel systems with logistic-type superlinear degradation
• A new (and optimal) result for the boundedness of a solution of a quasilinear chemotaxis-haptotaxis model (with a logistic source)
• Global solvability and stabilization to a cancer invasion model with remodelling of ECM
• Boundedness in a multi-dimensional chemotaxis-haptotaxis model with nonlinear diffusion
• A new result for global solvability of a two species cancer invasion haptotaxis model with tissue remodeling
• Asymptotic stability of spatial homogeneity in a haptotaxis model for oncolytic virotherapy
• Global existence and uniqueness of a parabolic haptotaxis model
• Global boundedness for a \(N\)-dimensional two species cancer invasion haptotaxis model with tissue remodeling
• Global boundedness of solutions to a chemotaxis-haptotaxis model with tissue remodeling
• Global boundedness in a three-dimensional chemotaxis-haptotaxis model
• A quasilinear chemotaxis-haptotaxis system: existence and blow-up results
• Global solvability and large time behavior to a chemotaxis-haptotaxis model with nonlinear diffusion
• Boundedness of solutions to a chemotaxis-haptotaxis model with nonlocal terms
• Boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion
• Boundedness in a three-dimensional chemotaxis-haptotaxis model with nonlinear diffusion
• Global classical solutions to a doubly haptotactic cross-diffusion system modeling oncolytic virotherapy
• Large-data solutions in a three-dimensional chemotaxis-haptotaxis system with remodeling of non-diffusible attractant: the role of sub-linear production of diffusible signal
• Global existence and boundedness in a chemotaxis-haptotaxis system with signal-dependent sensitivity
• A critical virus production rate for efficiency of oncolytic virotherapy
• A chemotaxis-haptotaxis system with haptoattractant remodeling: boundedness enforced by mild saturation of signal production
• Large time behavior of solutions to a fully parabolic chemotaxis-haptotaxis model in \(N\) dimensions
• A new result for global solvability and boundedness in the \(N\)-dimensional quasilinear chemotaxis model with logistic source and consumption of chemoattractant
• Asymptotic stability in a quasilinear chemotaxis-haptotaxis model with general logistic source and nonlinear signal production
• Boundedness in an attraction-repulsion chemotaxis system with both nonlinear signal production and consumption
• Optimal control for a chemotaxis-haptotaxis model in two space dimensions
• Global generalized solutions of a haptotaxis model describing cancer cells invasion and metastatic spread
• Large time behavior in the logistic Keller-Segel model via maximal Sobolev regularity
• Dominance of chemotaxis in a chemotaxis-haptotaxis model
• A new result for 2D boundedness of solutions to a chemotaxis-haptotaxis model with/without sub-logistic source
• Global existence for a chemotaxis-haptotaxis model with \(p\)-Laplacian
• Critical mass for infinite-time blow-up in a haptotaxis system with nonlinear zero-order interaction
• Global classical solutions to an oncolytic viral therapy model with triply haptotactic terms
• Modeling multiple taxis: tumor invasion with phenotypic heterogeneity, haptotaxis, and unilateral interspecies repellence
• Negligibility of haptotaxis effect in a chemotaxis-haptotaxis model
• Global solutions to a haptotaxis system with a potentially degenerate diffusion tensor in two and three dimensions
• Fluid interaction does not affect the critical exponent in a three-dimensional Keller-Segel-Stokes model
• Finite time blow-up in the higher dimensional parabolic-elliptic-ODE minimal chemotaxis-haptotaxis system
• Boundedness in a high-dimensional forager-exploiter model with nonlinear resource consumption by two species
• Boundedness and stabilization enforced by mild saturation of taxis in a producer-scrounger model
• Analysis of a two-dimensional triply haptotactic model with a fusogenic oncolytic virus and syncytia
• Solving a chemotaxis-haptotaxis system in 2D using generalized finite difference method
• Combined effects of nonlinear diffusion and gradient-dependent flux limitation on a chemotaxis-haptotaxis model
• Boundedness in a quasilinear fully parabolic Keller-Segel system via maximal Sobolev regularity
• Negligibility of haptotaxis on global dynamics in a chemotaxis-haptotaxis system with indirect signal production
• Does indirectness of signal production reduce the explosion-supporting potential in chemotaxis–haptotaxis systems? Global classical solvability in a class of models for cancer invasion (and more)
• Global dynamics in a fully parabolic chemotaxis system with logistic source
• Global boundedness and decay for a multi-dimensional chemotaxis-haptotaxis system with nonlinear diffusion
• Boundedness and asymptotic behavior of solutions to a chemotaxis-haptotaxis model in high dimensions
• Global boundedness of weak solutions to a chemotaxis-haptotaxis model with \(p\)-Laplacian diffusion
• Boundedness of solutions for a quasilinear chemotaxis-haptotaxis model
• Boundedness and global solvability to a chemotaxis-haptotaxis model with slow and fast diffusion
• Critical exponent to a cancer invasion model with nonlinear diffusion
• On a chemotaxis-type Solow-Swan model for economic growth with capital-induced labor migration
• Analysis of global dynamics in an attraction-repulsion model with nonlinear indirect signal and logistic source
• Boundedness in a fully parabolic chemotaxis-type Solow-Swan model
• Global classical solution and boundedness to a chemotaxis-haptotaxis model with re-establishment mechanisms
• Global attractors in a two-species chemotaxis system with two chemicals and logistic sources
• Asymptotic behaviour in a doubly haptotactic cross-diffusion model for oncolytic virotherapy
• Boundedness and large time behavior of solutions of a higher-dimensional haptotactic system modeling oncolytic virotherapy
• Global dynamics in a chemotaxis system involving nonlinear indirect signal secretion and logistic source
• Some further progress for boundedness of solutions to a quasilinear higher-dimensional chemotaxis-haptotaxis model with nonlinear diffusion
• Global Classical Solutions to a Predator-Prey Model with Nonlinear Indirect Chemotaxis Mechanism
• Global boundedness of solutions to a food chain model with nonlinear taxis sensitivity
• Boundedness in the higher dimensional attraction-repulsion chemotaxis-growth system
• Global boundedness of solutions to a quasilinear parabolic-parabolic Keller-Segel system with logistic source
• Global boundedness for a food chain model with general logistic source
• Boundedness of solutions to a quasilinear parabolic-parabolic chemotaxis model with variable logistic source
• Finite-time blow-up and global boundedness for chemotaxis system with strong logistic dampening
• Global boundedness in a parabolic-parabolic-elliptic attraction-repulsion chemotaxis system with nonlinear productions
• Global Solvability and Stability of an Alarm-Taxis System
• Global dynamics of a three-species spatial food chain model
• Global boundedness in an attraction-repulsion chemotaxis system involving nonlinear indirect signal mechanism
• Global weak solutions in a three-dimensional two-species cancer invasion haptotaxis model without cell proliferation
• Global boundedness in a chemotaxis-haptotaxis model with nonlinear diffusion and signal production
• Global boundedness in a two-competing-species chemotaxis system with two chemicals
• Global existence of a two-dimensional chemotaxis-haptotaxis model with remodeling of non-diffusible attractant

This page was built for publication: Boundedness in a three-dimensional chemotaxis-haptotaxis model

Report a bug (only for logged in users!)Click here to report a bug for this page (MaRDI item Q286427)