The Frederick P. Whiddon College of Medicine recently announced the recipients of the 2023 Faculty Intramural Grants Program Research Awards, which provide funds for basic science or translational research through an annual competitive program.
The awards allow faculty to develop new research ideas through seed funding, develop new critical preliminary data for revised extramural proposal submissions, or enable sustained research progress between extramural grant funding periods.
This year’s winners, who each received $50,000 in funding, are Luis del Pozo-Yauner, Ph.D., assistant professor of pathology; Jin H. Kim, D.V.M., Ph.D., assistant professor of microbiology and immunology; and Wito Richter, Ph.D., associate professor of biochemistry and molecular biology.
Luis del Pozo-Yauner, Ph.D. |
“Therefore, we hypothesize that the ovarian cancer cells that overexpress PERK protein constitute a subpopulation of polyploid giant cancer cells associated with a poor response to anti-tumor therapy and increased rate of tumor recurrence in ovarian cancer patients,” del Pozo-Yauner said. “Our research may help identify both new biomarkers and therapeutic targets that allow for better prognosis and therapy for ovarian cancer patients.”
Jin H. Kim, D.V.M., Ph.D. |
New drugs are being developed that target different parts of the flu virus, but their effectiveness needs to be tested. “The aim of this research is to find a combination of drugs that can treat the flu and extend the treatment window beyond what is currently possible,” Kim said. “We will test various drug combinations in a mouse model using bioluminescent flu virus to track the effectiveness of the treatments. The ultimate goal is to develop a safe and effective combination therapy for the flu that can be used in future clinical trials.”
Wito Richter, Ph.D. |
“As each PDE4 isoform serves unique and non-overlapping physiological and pathophysiological roles, targeting individual PDE4 proteins can serve to dissect the therapeutically beneficial from the side effects associated with current non-selective PDE4 inhibitors,” Richter said. “To this end, we will identify the specific PDE4 isoforms that represent the most promising therapeutic targets in metabolic syndromes, paving the way for development of subtype-selective PDE4 inhibitors as novel therapeutics targeting obesity and associated metabolic syndromes.”