Abstract
Multiscale modeling has now been well-accepted as a powerful tool to quantitatively represent, simulate, understand, and predict cancer progression and development across multiple biological scales. In this chapter, we focus on a specific type of multiscale cancer models where molecular signaling profiles are explicitly linked to the determination of cellular phenotypic changes. These models are particularly suitable for exploring the relationship between signaling dynamics within each individual cancer cell and the emergent cancer behavior on the multicellular level. We also discuss current challenges and future directions of this molecular signaling-incorporated multiscale cancer modeling approach.
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Abbreviations
- ABM:
-
Agent-based model or agent-based modeling
- EGF:
-
Epidermal growth factor
- EGFR:
-
EGF receptor
- EMT:
-
Epithelial–mesenchymal transition
- ERK:
-
Extracellular signal-regulated kinase
- NSCLC:
-
Non-small cell lung cancer
- ODE:
-
Ordinary differential equation
- PDE:
-
Partial differential equation
- PLCγ:
-
Phopholipase Cγ
- TGFβ:
-
Transforming growth factor β
- 2D:
-
Two-dimensional
- 3D:
-
Three-dimensional
- TEM:
-
Transendothelial migration
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Acknowledgments
This work has been supported in part by National Institutes of Health (NIH) grant CA 113004. VC acknowledges the NIH for support through 1U54CA143837, 1U54CA143907, and 1U54CA149196, and the National Science Foundation (NSF) for support under grant DMS-0818104.
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Wang, Z., Cristini, V. (2013). Integration of Molecular Signaling into Multiscale Modeling of Cancer. In: Gefen, A. (eds) Multiscale Computer Modeling in Biomechanics and Biomedical Engineering. Studies in Mechanobiology, Tissue Engineering and Biomaterials, vol 14. Springer, Berlin, Heidelberg. https://doi.org/10.1007/8415_2012_151
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DOI: https://doi.org/10.1007/8415_2012_151
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