TY - JOUR
T1 - Nonlinear simulation of tumor necrosis, neo-vascularization and tissue invasion via an adaptive finite-element/level-set method
AU - Zheng, X.
AU - Wise, S. M.
AU - Cristini, V.
N1 - Funding Information:
We are first and foremost grateful to Prof. John Lowengrub for useful and enjoyable discussions on the numerical methods. XZ is also grateful to Prof. Bernardo Cockburn for discussions on the LDG methods. We are grateful to Graduate Student Hermann Frieboes (Biomedical Engineering, UC Irvine) for providing experimental results on tumor spheroids. We are also grateful to the reviewers for their very insightful comments. We acknowledge the National Science Foundation, the Biomedical Engineering-College of Medicine Program and the Center for Complex Biological Systems both at UC Irvine for partial support. SW also acknowledges the Mathematics Department for partial support. We acknowledge the Biomedical Engineering Department, the Network and Academic Computing Systems and the Mathematics Department for computing time and assistance.
PY - 2005/3
Y1 - 2005/3
N2 - We present a multi-scale computer simulator of cancer progression at the tumoral level, from avascular stage growth, through the transition from avascular to vascular growth (neo-vascularization), and into the later stages of growth and invasion of normal tissue. We use continuum scale reaction-diffusion equations for the growth component of the model, and a combined continuum-discrete model for the angiogenesis component. We use the level set method for describing complex topological changes observed during growth such as tumor splitting and reconnection, and capture of healthy tissue inside the tumor. We use an adaptive, unstructured finite element mesh that allows for finely resolving important regions of the computational domain such as the necrotic rim, the tumor interface and around the capillary sprouts. We present full nonlinear, two-dimensional simulations, showing the potential of our virtual cancer simulator. We use microphysical parameters characterizing malignant glioma cells, obtained from recent in vitro experiments from our lab and from clinical data, and provide insight into the mechanisms leading to infiltration of the brain by the cancer cells. The results indicate that diffusional instability of tumor mass growth and the complex interplay with the developing neo-vasculature may be powerful mechanisms for tissue invasion.
AB - We present a multi-scale computer simulator of cancer progression at the tumoral level, from avascular stage growth, through the transition from avascular to vascular growth (neo-vascularization), and into the later stages of growth and invasion of normal tissue. We use continuum scale reaction-diffusion equations for the growth component of the model, and a combined continuum-discrete model for the angiogenesis component. We use the level set method for describing complex topological changes observed during growth such as tumor splitting and reconnection, and capture of healthy tissue inside the tumor. We use an adaptive, unstructured finite element mesh that allows for finely resolving important regions of the computational domain such as the necrotic rim, the tumor interface and around the capillary sprouts. We present full nonlinear, two-dimensional simulations, showing the potential of our virtual cancer simulator. We use microphysical parameters characterizing malignant glioma cells, obtained from recent in vitro experiments from our lab and from clinical data, and provide insight into the mechanisms leading to infiltration of the brain by the cancer cells. The results indicate that diffusional instability of tumor mass growth and the complex interplay with the developing neo-vasculature may be powerful mechanisms for tissue invasion.
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U2 - 10.1016/j.bulm.2004.08.001
DO - 10.1016/j.bulm.2004.08.001
M3 - Article
C2 - 15710180
AN - SCOPUS:13744255578
SN - 0092-8240
VL - 67
SP - 211
EP - 259
JO - Bulletin of Mathematical Biology
JF - Bulletin of Mathematical Biology
IS - 2
ER -