An evolutionary-game model of tumour-cell interactions: possible relevance to gene therapy

被引:52
作者
Bach, LA
Bentzen, SM
Alsner, J
Christiansen, FB
机构
[1] Mt Vernon Hosp, Gray Canc Inst, Grp Biostat Oncol, Northwood HA6 2JR, Middx, England
[2] Aarhus Univ, Dept Genet & Ecol, Aarhus, Denmark
[3] Aarhus Univ Hosp, Dept Expt Clin Oncol, DK-8000 Aarhus, Denmark
关键词
cell interactions; stable clonic heterogeneity; threshold proportion of cells; gene therapy; angiogenesis;
D O I
10.1016/S0959-8049(01)00246-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Evolutionary games have been applied as simple mathematical models of populations where interactions between individuals control the dynamics. Recently, it has been proposed to use this type of model to describe the evolution of tumour cell populations with interactions between cells. We extent the analysis to allow for synergistic effects between cells. A mathematical model of a tumour cell population is presented in which population-level synergy is assumed to originate through the interaction of triplets of cells. A threshold of two cooperating cells is assumed to be required to produce a proliferative advantage. The mathematical behaviour of this model is explored. Even this simple synergism (minor clustering effect) is sufficient to generate qualitatively different cell-population dynamics from the models published previously. The most notable feature of the model is the existence of an unstable internal equilibrium separating two stable equilibria. Thus, cells of a malignant phenotype can exist in a stable polymorphism, but may be driven to extinction by relatively modest perturbations of their relative frequency. The proposed model has some features that may be of interest to biological interpretations of gene therapy. Two prototypical strategies for gene therapy are suggested, both of them leading to extinction of the malignant phenotype: one approach would be to reduce the relative proportion of the cooperating malignant cell type below a certain critical value. Another approach would be to increase the critical threshold value without reducing the relative frequency of cells of the malignant phenotype. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
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页码:2116 / 2120
页数:5
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