Journal Information
Vol. 47. Issue S1.
2º Congresso CancerThera
(May 2025)
Vol. 47. Issue S1.
2º Congresso CancerThera
(May 2025)
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QUANTIFYING INTERSPECIFIC COMPETITION BETWEEN CANCER AND NORMAL CELLS USING USING NONLINEAR MIXED EFFECTS AND ORDINARY DIFFERENTIAL EQUATION MODELING
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Letícia Fernanda Alvesa, Mauro César Cafundó Moraisb, João Frederico Costa Azevedo Meyerc, Diego Samuel Rodriguesd
a PhD Program in Applied Mathematics, Universidade Estadual de Campinas (UNICAMP), Campinas, SP, Brazil
b Department of Clinical Analysis, Faculdade de Ciências Farmacêuticas, Universidade de São Paulo (USP), São Paulo, SP, Brazil
c Instituto de Matemática, Estatística e Computação Científica, Universidade Estadual de Campinas (UNICAMP), Campinas, SP, Brazil
d Faculdade de Tecnologia, Universidade Estadual de Campinas (UNICAMP), Limeira, SP, Brazil
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Vol. 47. Issue S1

2º Congresso CancerThera

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Abstract
Introduction/Justification

Tumor growth has been widely studied through various methodologies. In mathematical oncology, researchers use ordinary differential equations (ODEs) to analyze tumor dynamics. These models present meaningful parameters to link mathematical theory with experimental data. For in vitro cocultures, parameters quantifying cellular competition clarify interactions between tumor and normal cells.

Objectives

This research investigates the interaction between cancer and normal cells during competition, focusing on the in vitro growth of SK-MEL-147 (metastatic melanoma) and HaCaT (immortalized epithelial cells) cell lines. Using an ODE model with cell numbers as dependent variables, we quantify interspecific competition through the parameters α_{12} (impact of SK-MEL-147 on HaCaT) and α_{21} (impact of HaCaT on SK-MEL-147).

Materials and Methods

The in vitro cell growth experiments from Morais \textit{et al}., (2017), https://doi.org/10.1038/s41598-017-07553-6, allowed us to estimate parameters for Gatenby's 1996 ODE model. We used a nonlinear mixed effects model from NLMEModeling (https://doi.org/10.48550/arXiv.2011.06879) to account for observation errors and biological variability.

Results

The curve fitting matched the experimental data for both cell types. Parameter estimates showed that SK-MEL-147 cells experienced stronger inhibition from HaCaT cells than the reverse, suggesting normal cells hinder cancer cell growth upon contact.

Conclusion

Nonlinear mixed effects modeling successfully fit Gatenby's mathematical model to the experimental data, providing competition parameters that clarified interspecific interactions in tumor dynamics. Such models can predict cell growth behavior, supporting experimental design and reducing the need for preliminary \textit{in vitro} tests.

Keywords:
HaCaT Cell Lineage
SK-MEL-147 Cell Lineage
Skin cancer
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Idiomas
Hematology, Transfusion and Cell Therapy
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