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We propose a model for acid-mediated tumor invasion involving two different scales: the microscopic one, for the dynamics of intracellular protons and their exchange with their extracellular counterparts, and the macroscopic scale of interactions between tumor cell and normal cell populations, along with the evolution of extracellular protons. We also account for the tactic behavior of cancer cells, the latter being assumed to biase their motion according to a gradient of extracellular protons (following [2,31] we call this pH taxis). A time dependent (and also time delayed) carrying capacity for the tumor cells in response to the effects of acidity is considered as well. The global well posedness of the resulting multiscale model is proved with a regularization and fixed point argument. Numerical simulations are performed in order to illustrate the behavior of the model.
Cancer cell migration is an essential feature in the process of tumor spread and establishing of metastasis. It characterizes the invasion observed on the level of the cell population, but it is also tightly connected to the events taking place on the subcellular level. These are conditioning the motile and proliferative behavior of the cells, but are also influenced by it. In this work we propose a multiscale model linking these two levels and aiming to assess their interdependence. On the subcellular, microscopic scale it accounts for integrin binding to soluble and insoluble components present in the peritumoral environment, which is seen as the onset of biochemical events leading to changes in the cell's ability to contract and modify its shape. On the macroscale of the cell population this leads to modifications in the diffusion and haptotaxis performed by the tumor cells and implicitly to changes in the tumor environment. We prove the (local) well posedness of our model and perform numerical simulations in order to illustrate the model predictions.
Starting from the two-scale model for pH-taxis of cancer cells introduced in [1], we consider here an extension accounting for tumor heterogeneity w.r.t. treatment sensitivity and a treatment approach including chemo- and radiotherapy. The effect of peritumoral region alkalinization on such therapeutic combination is investigated with the aid of numerical simulations.