Hybrid multiscale modeling and prediction of cancer cell behavior
Authored by Jafar Habibi, Mohammad Hossein Zangooei
Date Published: 2017
DOI: 10.1371/journal.pone.0183810
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Other Narrative
Mathematical description
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Abstract
Background
Understanding cancer development crossing several spatial-temporal
scales is of great practical significance to better understand and treat
cancers. It is difficult to tackle this challenge with pure biological
means. Moreover, hybrid modeling techniques have been proposed that
combine the advantages of the continuum and the discrete methods to
model multiscale problems.
Methods
In light of these problems, we have proposed a new hybrid vascular model
to facilitate the multiscale modeling and simulation of cancer
development with respect to the agent-based, cellular automata and
machine learning methods. The purpose of this simulation is to create a
dataset that can be used for prediction of cell phenotypes. By using a
proposed Q-learning based on SVR-NSGA-II method, the cells have the
capability to predict their phenotypes autonomously that is, to act on
its own without external direction in response to situations it
encounters.
Results
Computational simulations of the model were performed in order to
analyze its performance. The most striking feature of our results is
that each cell can select its phenotype at each time step according to
its condition. We provide evidence that the prediction of cell
phenotypes is reliable.
Conclusion
Our proposed model, which we term a hybrid multiscale modeling of cancer
cell behavior, has the potential to combine the best features of both
continuum and discrete models. The in silico results indicate that the
3D model can represent key features of cancer growth, angiogenesis, and
its related micro-environment and show that the findings are in good
agreement with biological tumor behavior. To the best of our knowledge,
this paper is the first hybrid vascular multiscale modeling of cancer
cell behavior that has the capability to predict cell phenotypes
individually by a self-generated dataset.
Tags
Agent-based model
Angiogenesis
Heterogeneity
Mathematical-model
Automaton model
Multicellular patterns
Solid tumor
Phenotypes
Avascular tumor-growth
Brain cancer