Jane Ishmael smiles at camera outside

Jane Ishmael

Professor

Research/Career Interests

Our research focuses on understanding the functional relationship between autophagy (“self-eating”) and cell death signaling in brain tumor cells. Glioblastoma multiforme is the most common malignant primary tumor of the central nervous system and remains very difficult to treat. These tumors arise from astrocytes and have many biological characteristics that allow them to evade cell death. We utilize a range of human cancer cell types and genetically modified mouse embryonic fibroblasts (MEFs) to determine how cells use autophagy as a survival response to stress. Our research interests are closely aligned with the drug discovery efforts in the College of Pharmacy, and we study a number of unique compounds that have arisen in nature in diverse and unusual ecosystems. The main projects in the Ishmael laboratory are currently centered around structures with anticancer potential that were discovered by Drs. Kerry McPhail and Taifo Mahmud at collection sites in Panama, South Africa, Indonesia and the Red Sea.  By working at the interface of Medicinal Chemistry and Pharmacology we seek to understand the potential of these naturally occurring structures to modulate autophagy, inhibit cellular proliferation and induce apoptotic or alternate modes of cancer cell death.  Our long-term goal is to characterize new chemical entities with the potential to inspire drug development for and identify new cellular targets for cancer chemotherapy.

 

Credentials

National Institute on Drug Abuse Postdoctoral Fellow, 1996-1999 Oregon State University, Postdoctoral Training, 1995-1999 Oregon State University, Ph.D., 1995 University of Bradford, England, Bachelor of Science, 1988

Contact

1601 SW Jefferson Avenue
Pharmacy Building 411
97331 OR
United States

Research Topics & Highlights
Research Highlights

Dr. Ishmael’s research focuses on the use of new chemical entities from marine organisms and fungi as tool compounds to disrupt cell signaling and proteostasis in human cancer cells. With a special interest in glioblastoma, our goal is to identify and validate novel druggable targets for the treatment of human disease.