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A mathematical and computer model of cancer growth
Colloquium| Speaker: | Dr. Vittorio Cristini, University of Minnesota |
| Location: | 693 Kerr |
| Start time: | Tue, Jan 22 2002, 4:10PM |
Description
I will present and discuss the current status of a mathematical and
computer model of cancer growth under development in my research
group. The motivation of this work is to identify and analyze diagnostic
and treatment strategies through direct in silico simulations. Once
completed, this sophisticated computer model will provide a physician with
a tool that simulates the development of a tumor corresponding to a
specific patient's clinical history. In particular, the efficacy of
different treatment strategies will be assessed by direct simulation.
The development of a realistic computer model is now possible due to the
recent advances by our group in adaptive numerical modeling and simulation
techniques for complex evolving microstructures. These new techniques are
capable of describing, for example, the complex shape of a solid carcinoma
characterized by invasive fingering and metastasization.
The model will include all phases of growth that have been identified in
the biological and biomedical literature:
1. the initial, diffusion-driven growth to a dormant multicell spheroid
state, regulated by the transport of nutrient chemical species;
2. necrosis, and the formation of a core of dead tumor cells, due to the
transport of growth inhibitor factors;
3. angiogenesis, or blood vessel formation in the tumor, triggered by tumor
angiogenetic factors, and endothelial cell migration and proliferation in
response to the growth of the multicell spheroid;
4. vascular growth of malignant carcinoma with invasive fingering and
metastasization.
I will present the current status of the model, capable of simulating
phases 1, 2, and 4, but not the process of angiogenesis. I will then
demonstrate how the assumptions and predictions of the model have been
validated and refined, for the case of avascular growth (1 and 2), by
direct comparison with experimental observations of in vitro and in vivo
tumor growth. I will also discuss how angiogenesis will be included in our
model.
