Abstract
BackgroundGlioblastoma multiforme (GBM) is a devastating brain cancer for which there is no known cure. Its malignancy is due to rapid cell division along with high motility and invasiveness of cells into the brain tissue. Simple 2-dimensional laboratory assays (e.g., a scratch assay) commonly are used to measure the effects of various experimental perturbations, such as treatment with chemical inhibitors. Several mathematical models have been developed to aid the understanding of the motile behavior and proliferation of GBM cells. However, many are mathematically complicated, look at multiple interdependent phenomena, and/or use modeling software not freely available to the research community. These attributes make the adoption of models and simulations of even simple 2-dimensional cell behavior an uncommon practice by cancer cell biologists.ResultsHerein, we developed an accurate, yet simple, rule-based modeling framework to describe the in vitro behavior of GBM cells that are stimulated by the L1CAM protein using freely available NetLogo software. In our model L1CAM is released by cells to act through two cell surface receptors and a point of signaling convergence to increase cell motility and proliferation. A simple graphical interface is provided so that changes can be made easily to several parameters controlling cell behavior, and behavior of the cells is viewed both pictorially and with dedicated graphs. We fully describe the hierarchical rule-based modeling framework, show simulation results under several settings, describe the accuracy compared to experimental data, and discuss the potential usefulness for predicting future experimental outcomes and for use as a teaching tool for cell biology students.ConclusionsIt is concluded that this simple modeling framework and its simulations accurately reflect much of the GBM cell motility behavior observed experimentally in vitro in the laboratory. Our framework can be modified easily to suit the needs of investigators interested in other similar intrinsic or extrinsic stimuli that influence cancer or other cell behavior. This modeling framework of a commonly used experimental motility assay (scratch assay) should be useful to both researchers of cell motility and students in a cell biology teaching laboratory.
Highlights
Glioblastoma multiforme (GBM) is a devastating brain cancer for which there is no known cure
We have shown that the neural adhesion molecule L1CAM (L1) stimulates GBM cell motility and invasion both in vitro and in vivo using a variety of approaches [1, 10, 17]
If mechanisms controlling GBM cell motility and invasion can be modeled and simulated, this likely will aid in experimental design and predicting outcomes of experimental manipulations
Summary
Glioblastoma multiforme (GBM) is a devastating brain cancer for which there is no known cure. Many are mathematically complicated, look at multiple interdependent phenomena, and/or use modeling software not freely available to the research community. These attributes make the adoption of models and simulations of even simple 2-dimensional cell behavior an uncommon practice by cancer cell biologists. GBM cells aggressively invade surrounding brain tissue from the start, so that cells invariably are left behind after surgical resection. These cells are resistant to adjuvant chemo- or radiation-therapy, so that they initiate tumor regrowth. If mechanisms controlling GBM cell motility and invasion can be modeled and simulated, this likely will aid in experimental design and predicting outcomes of experimental manipulations
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