Abstract

In this paper, we focused on numerical solutions of carcinogenesis mutations models that are based on reaction-diffusion systems and Lotka-Volterra food chains. We consider the case with one and two-stages of mutations with appropriate initial conditions and the zero-flux boundary conditions. The main purpose is to construct a stable discretization scheme, which allows much accuracy than those of a standard approach. To this end, we use the spectral method to postprocess numerical solutions for the proposed model by using some classical methods for solving differential equations. The implementation of the algorithm is simple and it does not need to solve the linear or nonlinear system (in case the model is nonlinear). We simulate the one and two-stage carcinogenesis mutations model and compared the results with previously published ones.

Highlights

  • The struggle for finding an effective and permanent cure for tumor continues to challenge scientists has been made by a lot of progresses in discovering new methodologies which are helpful in successful treatments to reduce and even clear tumors

  • We focused on numerical solutions of carcinogenesis mutations models that are based on reaction-diffusion systems and Lotka-Volterra food chains

  • The immune response to tumors depends on how antigenic the tumor is

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Summary

Introduction

The struggle for finding an effective and permanent cure for tumor continues to challenge scientists has been made by a lot of progresses in discovering new methodologies which are helpful in successful treatments to reduce and even clear tumors. We study a simple model of carcinogenesis mutations of DNA, which originally comes from [3]. Was studied in [4,5,6,7,8,9], which describe a process of carcinogenesis mutations with n different steps of mutations (from normal to malignant cells). The model is expressed in terms of system of partial differential equation, in which the latest stage of mutation has different forms depending on whether it has growth advantage in favorable or competitive conditions or disadvantage of growth in unfavorable and competitive conditions. For simplicity in this paper, we only consider the latest stage in unfavorable conditions, as in the case of favorable conditions there is no possibility to cure the disease without any treatment.

Formulation of the Model
Formulation of One and Two-Stage Mutation
Finite Difference Scheme
Postprocessing
LN 1 xj
Concluding Remarks
Full Text
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