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. 2010 Jun 15:7:21.
doi: 10.1186/1742-4682-7-21.

Chemotherapy in conjoint aging-tumor systems: some simple models for addressing coupled aging-cancer dynamics

Affiliations

Chemotherapy in conjoint aging-tumor systems: some simple models for addressing coupled aging-cancer dynamics

Mitra S Feizabadi et al. Theor Biol Med Model. .

Abstract

Background: In this paper we consider two approaches to examining the complex dynamics of conjoint aging-cancer cellular systems undergoing chemotherapeutic intervention. In particular, we focus on the effect of cells growing conjointly in a culture plate as a precursor to considering the larger multi-dimensional models of such systems. Tumor cell growth is considered from both the logistic and the Gompertzian case, while normal cell growth of fibroblasts (WI-38 human diploid fibroblasts) is considered as logistic only.

Results: We demonstrate, in a simple approach, how the interdependency of different cell types in a tumor, together with specifications of for treatment, can lead to different evolutionary patterns for normal and tumor cells during a course of therapy.

Conclusions: These results have significance for understanding appropriate pharmacotherapy for elderly patients who are also undergoing chemotherapy.

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Figures

Figure 1
Figure 1
Blue curve: Evolution of normal cells. Purple curve: Evolution of tumor cells. Common parameters: rN = 0.4, rT = 0.3, KT = 1.2.106, KN = 106. Left: There is no interaction between normal cells and tumor cells (both populations undergo logistic growth), k = 0, β = 0. Right: Normal and tumor cells are allowed to interact with each other, k = 1, β = 2, ρ0 = 1, ρ1 = 1000, T* = 3.105, N0 = 1, T0 = 1. The mini-window magnifies the behavior of normal and tumor cells close to the critical size of the tumor. As the size of the tumor cells T exceed the critical size, T* (dashed line), the size of normal cells N starts decreasing.
Figure 2
Figure 2
The evolution of normal cells and tumor cells during the phase of therapy. The drug is considered to be static. First row: the drug does not have any effects on normal cells, aN(1 - emu) = 0, and aT(1 - emu) = 0.01 (red), 0.05 (green), 0.1 (black). Second row: the drug kills both normal and tumor cells with more killing strength on the tumor cells. Blue represents the untreated system when aN(1 - emu) = 0 = aT(1 - emu) = 0. From there, the response of the tumor cells is considered to be constant, aT(1 - emu) = 0.1, while a variation is considered for the response of normal cells as: aN(1 - emu) = 0.01 (red), 0.05, (green), 0.1 (black). Third row: the drug kills both normal and tumor cells with more killing strength on normal cells. blue is untreated system when aN(1 - emu) = 0 = aT(1 - emu) = 0, From there, the response of the normal cells is considered to be constant, aN(1 - emu) = 0.1, while a variation is considered for the response of the normal cells as: aT(1 - emu) = 0.01 (red), 0.05, (green), 0.1 (black). The rest of the parameters are similar to the common parameter introduced in Figure [1].
Figure 3
Figure 3
The evolution of normal cells and tumor cells during the phases of therapy. The drug is considered to be dynamic and its concentration diffuses exponentially over time. u0 is the initial value of the drug and d is the decaying rate, and m is linked to pharmacokinetics and considered to be 1 in this study. The drug does not have any effect on normal cells, aN(1 - emu) = 0, aT = 0.1. First row: The evolution of normal and tumor cells is simulated for different drug decaying rates. u0 = 1, and untreated (blue), d = 0.1 (red), 0.5 (green), 1 (black), and 2 (brown). As can be seen, the system tends to behave as untreated as the decaying rate increases. Second row: Same parameters in the first row except the initial value of the drug is increased, u0 = 3, which maintains the diffusion behavior of the drug leading to slower growth for the tumor cells and a delay in entering the inhibition phase for the normal cells. The rest of the parameters are similar to the common parameter introduced in Figure [1].
Figure 4
Figure 4
Model 2. Top-Blue: Evolution of normal cells, Purple: Evolution of tumor cells. Common parameters: rN = 0.4, h = 105, γ = 0.083, KN = 106. Top left: there is no interaction between normal cells and tumor cells k = 0, β = 0. Tumor cells show a higher increasing rate at the beginning compared to the normal cells. Top right: normal and tumor cells are allowed to interact, k = 1, β = 2, ρ0 = 1, ρ1 = 1000, T* = 3.105, N0 = 1, T0 = 1. Fast growing tumor cells force the normal passes the critical size of tumor cells quickly and force normal cells enter to the inhibition phase in a short time. Down: The evolution of normal cells and tumor cells during the phase of therapy. The drug is considered to be static. Down Left: the drug does not have any effects on normal cells, aN(1 - emu) = 0, and aT(1 - emu) = 0.0 (Blue-untreated system), 0.1 (red), and 0.17 (green). Effect of the drug in slower growth of tumor cells and a delay in entering the inhibition phase for the normal cells can be detected.

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