Undergraduate Research Assistant
CurrentMy project utilizes a hyaluronic acid hydrogel matrix to mimic the biophysical characteristics of the brain tumor microenvironment to study drug response in brain metastatic breast cancer (BMBC) spheroids. Two different stiffnesses are used to mimic the normal brain (soft, ~0.4 kPa) and tumor (stiff, ~4.5 kPa) environments. Both MDA-MB-231Br and BT474Br spheroids cultured on soft gels exhibited a resistant phenotype with no observed response to drug treatment, while spheroids cultured on stiff gels responded to the treatment. My findings demonstrate that drug resistance in the soft environment was mediated, in part, by serum/glucocorticoid-regulated kinase 1 (SGK-1), as inhibition of SGK-1 resulted in a response to treatment. Overall, such platforms provide a tool to further understand drug resistance mechanisms mediated by the tumor microenvironment in BMBC spheroids.