ALBERT

Description: Mathematical Oncology has emerged as a research field that applies either continuous or discrete models to mathematically describe cancer-related phenomena. Such methods are usually expressed in terms of differential equations, however tumor composition involves specific cellular structure and can demonstrate probabilistic nature, often requiring tailor-made approaches. In this context, cell-based models allow monitoring independent single parameters, which might vary in both time and space. By relying on extant tumor growth models in the literature, this study introduces cellular-automata simulation strategies that admit heterogeneous cell population while capturing both single-cell and cluster-cell behaviors. In this agent-based computational model, tumor cells are limited to follow four possible courses of action, namely: proliferation, migration, apoptosis or quiescence. Despite the apparent simplicity of those actions, the model can represent different complex tumor features depending on parameter settings. This study virtualized five different scenarios, showcasing model capabilities of representing tumor dynamics including alternate dormancy periods, cell death instability and cluster formation. Implementation techniques are also explored together with prospective model expansion towards deterministic features. The proposed stochastic cellular automaton model is able to effectively simulate different scenarios regarding tumor growth effectively, figuring as an interesting tool for in silico modeling, with promising capabilities of expansion to support research in mathematical oncology, thus improving diagnosis tools and/or personalized treatment.