scholarly journals A mathematical model of tumor growth by diffusion

1989 ◽  
Vol 94 (1) ◽  
pp. 155 ◽  
Author(s):  
John A. Adam
2018 ◽  
Author(s):  
Jeffrey West ◽  
Paul K. Newton

AbstractA tumor is made up of a heterogeneous collection of cell types all competing on a fitness landscape mediated by micro-environmental conditions that dictate their interactions. Despite the fact that much is known about cell signaling and cellular cooperation, the specifics of how the cell-to-cell coupling and the range over which this coupling acts affect the macroscopic tumor growth laws that govern total volume, mass, and carrying capacity remain poorly understood. We develop a statistical mechanics approach that focuses on the total number of possible states each cell can occupy, and show how different assumptions on correlations of these states gives rise to the many different macroscopic tumor growth laws used in the literature. Although it is widely understood that molecular and cellular heterogeneity within a tumor is a driver of growth, here we emphasize that focusing on the functional coupling of these states at the cellular level is what determines macroscopic growth characteristics.Significance statementA mathematical model relating tumor heterogeneity at the cellular level to tumor growth at the macroscopic level is described based on a statistical mechanics framework. The model takes into account the number of accessible states available to each cell as well as their long-range coupling (population cooperation) to other cells. We show that the degree to which cell populations cooperate determine the number of independent cell states, which in turn dictates the macroscopic (volumetric) growth law. It follows that targeting cell-to-cell interactions could be a way of mitigating and controlling tumor growth.


2010 ◽  
Author(s):  
Jiang ji ◽  
Guangde tu ◽  
Mei zou

2019 ◽  
Vol 29 (01) ◽  
pp. 1950009 ◽  
Author(s):  
Zonghong Feng ◽  
Xinxing Wu ◽  
Luo Yang

This paper studies a mathematical model for the interaction between tumor cells and Cytotoxic T lymphocytes (CTLs) under drug therapy. We obtain some sufficient conditions for the local and global asymptotical stabilities of the system by using Schur–Cohn criterion and the theory of Lyapunov function. In addition, it is known that the system without any treatment may undergo Neimark–Sacker bifurcation, and there may exist a chaotic region of values of tumor growth rate where the system exhibits chaotic behavior. So it is important to narrow the chaotic region. This may be done by increasing the intensity of the treatment to some extent. Moreover, for a fixed value of tumor growth rate in the chaotic region, a threshold value [Formula: see text] is predicted of the treatment parameter [Formula: see text]. We can see Neimark–Sacker bifurcation of the system when [Formula: see text], and the chaotic behavior for tumor cells ends and the system becomes locally asymptotically stable when [Formula: see text].


1973 ◽  
Vol 95 (3) ◽  
pp. 324-327 ◽  
Author(s):  
Leon Glass

A mathematical model which reproduces several qualitative features of cancerous tumor growth is proposed. The onset of unstable growth is characterized by a dimensionless number, which is defined in terms of the parameters describing the system. Patterns of mitotic activity of the model system are compared with experimentally observed patterns of mitotic activity in cancerous tissues.


2020 ◽  
Vol 2020 ◽  
pp. 1-5
Author(s):  
Xiaofei Yang ◽  
Bo Lu

In this paper, we consider a gradient-driven mathematical model of antiangiogenesis in tumor growth. In the model, the movement of endothelial cells is governed by diffusion of themselves and chemotaxis in response to gradients of tumor angiogenic factors and angiostatin. The concentration of tumor angiogenic factors and angiostatin is assumed to diffuse and decay. The resulting system consists of three parabolic partial differential equations. In the present paper, we study the global existence and boundedness of classical solutions of the system under homogeneous Neumann boundary conditions.


Author(s):  
Shihe Xu

AbstractIn this paper, a mathematical model for a solid avascular tumor growth under the effect of periodic therapy is studied. Necessary and sufficient conditions for the global stability of tumor free equilibrium are given. The conditions under which there exists a unique periodic solution to the model are determined and we also show that the unique periodic solution is global attractor of all other positive solutions.


2012 ◽  
Vol 2012 ◽  
pp. 1-19 ◽  
Author(s):  
F. A. Rihan ◽  
M. Safan ◽  
M. A. Abdeen ◽  
D. Abdel Rahman

We provide a family of ordinary and delay differential equations to model the dynamics of tumor-growth and immunotherapy interactions. We explore the effects of adoptive cellular immunotherapy on the model and describe under what circumstances the tumor can be eliminated. The possibility of clearing the tumor, with a strategy, is based on two parameters in the model: the rate of influx of the effector cells and the rate of influx of IL-2. The critical tumor-growth rate, below which endemic tumor does not exist, has been found. One can use the model to make predictions about tumor dormancy.


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