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Emergent Behaviors from a Cellular Automaton Model for Invasive Tumor Growth in Heterogeneous Microenvironments

Overview of attention for article published in PLoS Computational Biology, December 2011
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Title
Emergent Behaviors from a Cellular Automaton Model for Invasive Tumor Growth in Heterogeneous Microenvironments
Published in
PLoS Computational Biology, December 2011
DOI 10.1371/journal.pcbi.1002314
Pubmed ID
Authors

Yang Jiao, Salvatore Torquato

Abstract

Understanding tumor invasion and metastasis is of crucial importance for both fundamental cancer research and clinical practice. In vitro experiments have established that the invasive growth of malignant tumors is characterized by the dendritic invasive branches composed of chains of tumor cells emanating from the primary tumor mass. The preponderance of previous tumor simulations focused on non-invasive (or proliferative) growth. The formation of the invasive cell chains and their interactions with the primary tumor mass and host microenvironment are not well understood. Here, we present a novel cellular automaton (CA) model that enables one to efficiently simulate invasive tumor growth in a heterogeneous host microenvironment. By taking into account a variety of microscopic-scale tumor-host interactions, including the short-range mechanical interactions between tumor cells and tumor stroma, degradation of the extracellular matrix by the invasive cells and oxygen/nutrient gradient driven cell motions, our CA model predicts a rich spectrum of growth dynamics and emergent behaviors of invasive tumors. Besides robustly reproducing the salient features of dendritic invasive growth, such as least-resistance paths of cells and intrabranch homotype attraction, we also predict nontrivial coupling between the growth dynamics of the primary tumor mass and the invasive cells. In addition, we show that the properties of the host microenvironment can significantly affect tumor morphology and growth dynamics, emphasizing the importance of understanding the tumor-host interaction. The capability of our CA model suggests that sophisticated in silico tools could eventually be utilized in clinical situations to predict neoplastic progression and propose individualized optimal treatment strategies.

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The data shown below were compiled from readership statistics for 114 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 6 5%
France 2 2%
United Kingdom 1 <1%
Germany 1 <1%
Japan 1 <1%
Spain 1 <1%
Unknown 102 89%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 28 25%
Researcher 27 24%
Student > Master 12 11%
Student > Bachelor 10 9%
Professor 8 7%
Other 15 13%
Unknown 14 12%
Readers by discipline Count As %
Agricultural and Biological Sciences 31 27%
Biochemistry, Genetics and Molecular Biology 13 11%
Computer Science 12 11%
Physics and Astronomy 11 10%
Engineering 11 10%
Other 18 16%
Unknown 18 16%