Utilizing organoid models for PDAC drug screening to identify compounds inducing prooxidative stress and inhibiting glutamine metabolism, this solution aims to enhance therapeutic efficacy by targeting critical tumor pathways.
The research seeks to revolutionize pancreatic ductal adenocarcinoma (PDAC) drug screening by utilizing organoid models. These models help identify compounds that simultaneously induce prooxidative stress and inhibit glutamine metabolism. This dual-action mechanism is expected to target crucial pathways in tumor progression, potentially leading to more effective PDAC therapies and improved patient outcomes.
The technology readiness level is stated as 4, indicating the solution has been validated in laboratory environments. Future plans include testing in patient-derived xenograft (PDX) and syngeneic models to ensure clinical relevance.
USC is a large, comprehensive private research university in Los Angeles, anchored by two urban campuses and an academic health system. Industry engages through applied research institutes such as the Information Sciences Institute, co-located engineering and clinical facilities, and flexible sponsored research contracting. Proximity to the region’s aerospace, media, and biotech corridors provides access to testbeds, talent, and pilot-scale partners across the greater L.A. innovation economy. Research is supported by competitive federal funding from NIH, NSF, and other major agencies alongside significant industry-sponsored awards. A dedicated technology transfer office supports IP strategy, licensing, corporate partnerships, and venture formation.