Biomechanics of Collective Cell Migration in Cancer Progression -- Experimental and Computational Methods
arXiv:1903.04921
Abstract
Cell migration is essential for regulating many biological processes in physiological or pathological conditions, including embryonic development and cancer invasion. In vitro and in silico studies suggest that collective cell migration is associated with some biomechanical particularities, such as restructuring of extracellular matrix, stress and force distribution profiles, and reorganization of cytoskeleton. Therefore, the phenomenon could be understood by an in-depth study of cells' behavior determinants, including but not limited to mechanical cues from the environment and from fellow travelers. This review article aims to cover the recent development of experimental and computational methods for studying the biomechanics of collective cell migration during cancer progression and invasion. We also summarized the tested hypotheses regarding the mechanism underlying collective cell migration enabled by these methods. Together, the paper enables a broad overview on the methods and tools currently available to unravel the biophysical mechanisms pertinent to cell collective migration, as well as providing perspectives on future development towards eventually deciphering the key mechanisms behind the most lethal feature of cancer.
References in corpus (12)
- Novel type of phase transition in a system of self-driven particles
- A density-independent glass transition in biological tissues
- Motility-driven glass and jamming transitions in biological tissues
- Phase transition in the collective migration of tissue cells: experiment and model
- Active Jamming: Self-propelled soft particles at high density
- Universal geometric constraints during epithelial jamming
- Jamming of Deformable Polygons
- Correlating Cell Shape and Cellular Stress in Motile Confluent Tissues
- Inference of internal stress in a cell monolayer
- Emergent Behaviors from A Cellular Automaton Model for Invasive Tumor Growth in Heterogeneous Microenvironments
- Soft yet sharp interfaces in a vertex model of confluent tissue
- Modeling Three-dimensional Invasive Solid Tumor Growth in Heterogeneous Microenvironment under Chemotherapy