Project Archive - These research projects were formerly active avenues of investigation that are currently not being actively pursued within the Weis Lab.
We began with the hypothesis that interactions between cancer and tissue at the macroscopic level can be described by a coupled reactive-diffusive mechanics system, where tumor cells grow and diffuse in space depending on their mechanical environment. Rather than use this system to simulate tumor growth de novo, the Weis Lab works to leverage rich non-invasive imaging data sources available to make these models patient-specific and data driven. This has led to work developing a mathematical approach to interpret quantitative in vivo imaging data using biomathematical models of tumor growth in order to characterize and predict response to neoadjuvant chemotherapy based on early measurements. The Weis Lab investigates the use of these methods in both pre-clinical and clinical settings using 3D spheroid/organoid cancer model systems imaged using live-cell fluorescence microscopy and quantitative MRI in patients, respectively.
Patients with intracranial metastases often undergo stereotactic radiosurgery (e.g. GammaKnife) for local control. Following treatment, some patients develop radiation-induced necrosis, which appears radiographically similar to tumor recurrence on follow-up imaging. Both may appear as an enhancing lesion in contrast-enhanced MR imaging with surrounding fluid abnormality, complicating diagnostic and therapeutic efforts. The Weis Lab has developed a spatiotemporal model of tumor growth to parameterize tumor growth kinetics, based on contrast-enhanced serial MR imaging. Differences between patients with tumor recurrence and radiation-induced necrosis can be identified when comparing the biophysical model-based parameters, suggesting the potential to non-invasively distinguish between diagnoses in a biophysical model-based image analysis framework.
Mechanical investigations within the Weis Lab focus on studying cancer from a mechanics and mathematical modeling background to explore tissue-level mechanical stiffness imaging biomarkers in breast cancer. The Weis Lab has developed novel computational methodologies to assess tissue-level mechanical elasticity in breast cancer clinical and preclinical models based on anatomical magnetic resonance images collected before and after the application of a quasi-static mechanical compression. In an extension to the methodology, we have also investigated the use of the method in clinical cancer patients using gravitational excitation as a deformation source to drive model-based estimation of mechanical tissue stiffness markers.