Overall, the project is designed to (1) add insights as to the biophysical mechanisms that link molecular- and cell-scale variations in the tumor and the microenvironment to the tumor's growth, (2) develop techniques that allow us to readily incorporate cutting-edge experimental measurements into the multi-scale model and thus more quickly determine their impact on overall tumor progression and response to therapy, (3) investigate and quantify the spatiotemporal dynamics of tumor response to therapy, (4) improve the in vivo-in silico development feedback loop that forms the backbone of true integrative modeling, and so (4) push the frontier of multi-scale, integrative cancer modeling. In order to quantify the relationships between complex cancer phenomena at different scales, we harness the advantages of both discrete and continuum modeling approaches by employing hybrid modeling. We implement hybrid, multi-scale algorithms as the next stage of cancer modeling in general, and lymphoma and leukemia modeling in particular. This involves dynamically coupling tumor-scale models and molecular/cell-scale models developed by Cristini, Macklin and coworkers with cell signaling and evolutionary/hereditary models developed by Research Project 2. This also requires integration with state of- the-art intravital time-course measurements of tumor growth, vascularization, and response to chemotherapy by Gambhir and co-workers. These experiments will (1) provide us with first-hand biological data that will shape the model development, (2) provide us with precise measurements of key model parameters that uniquely constrain the modeling framework, (3) provide additional, independent tests for model validation and testing, and (4) provide an opportunity for true integrative modeling, where our first round of investigating the calibrated model leads to follow-up experiments to test new cancer biology hypotheses and improve the multiscale model.

Public Health Relevance

We bring together a team of leading experts in mathematical modeling of cancer and multiple scales (PI Cristini) with a team of cancer biologists with innovative, cutting-edge in vivo tumor imaging methods (PI Gambhir) to conduct integrative modeling, where experiments shape model development, and subsequent simulations generate testable hypotheses for further experiments.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54CA143907-02
Application #
8182432
Study Section
Special Emphasis Panel (ZCA1)
Project Start
Project End
Budget Start
2010-08-01
Budget End
2011-07-31
Support Year
2
Fiscal Year
2010
Total Cost
$375,857
Indirect Cost
Name
University of Southern California
Department
Type
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
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Tennill, Thomas A; Gross, Mitchell E; Frieboes, Hermann B (2017) Automated analysis of co-localized protein expression in histologic sections of prostate cancer. PLoS One 12:e0178362
Ware, Matthew J; Curtis, Louis T; Wu, Min et al. (2017) Pancreatic adenocarcinoma response to chemotherapy enhanced with non-invasive radio frequency evaluated via an integrated experimental/computational approach. Sci Rep 7:3437

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