George C. Prendergast (born 1961) is an American biomedical scientist. His research has focused on cancer pathobiology and immunology.[1] Since 2004, he has been the President and CEO of
Lankenau Institute for Medical Research, a cancer-focused research center in the U.S.[2][3][4] He is also the co-director of the Program in Cancer Cell Biology & Signaling at the Sidney Kimmel Cancer Center,
Thomas Jefferson University.[5]
Education
Prendergast earned his bachelor's degree in biochemistry from the
University of Pennsylvania, his master's degree in molecular biophysics and biochemistry from
Yale University and his PhD in molecular biology from
Princeton University.[6][7][8] He was later an American Cancer Society postdoctoral fellow at the Howard Hughes Medical Institute at New York University Medical Center before working in the Department of
Cancer Research at Merck.[9][10]
Career
In 1993, Prendergast joined the faculties of The Wistar Institute and the Department of Genetics at the
University of Pennsylvania. In 1999, he also became a Senior Director at the DuPont Pharmaceuticals Company.[11][12]
In 2002, he moved his groups at Wistar and DuPont to the Lankenau Institute for Medical Research (LIMR) and became the President and CEO there in 2004.[13] At LIMR, Prendergast created an organizational model for nonprofit biomedical research termed the acapreneurial™ model, whose stated aim is to balance academic studies with invention, product development and partnered entrepreneurialism.[14][15][16][17]
Prendergast's current research focuses on new uses of IDO1 inhibitory drugs in medicine, investigations of the IDO2 enzyme in cancer and autoimmunity, and therapeutic antibodies that target the disease severity modifier genes Bin1 and RhoB to broadly treat autoimmune disorders and diabetic complications.
His research team pioneered the early discovery and development of experimental drugs that inhibit the tryptophan catabolizing enzyme IDO1 as a new type of oral immunotherapy for cancer,[18] currently under study worldwide.[19]
In 2008, Prendergast was recognized as one of the 250 most influential alumni of
Princeton University.[20] From 2010-2017, Prendergast was Editor-in-Chief of Cancer Research, a journal of the American Association for Cancer Research, one of the most cited in the field.[21] In 2018, Prendergast was named The Havens Chair in Biomedical Research by the Lankenau Medical Center Foundation.[22]
Muller, AJ; Duhadaway, JB; Donover, PS; Sutanto-Ward, E; Prendergast, GC (2005). "Inhibition of indoleamine 2,3-dioxygenase, an immunoregulatory target of the cancer suppression gene Bin1, potentiates cancer chemotherapy". Nature Medicine. 11 (3): 312–9.
doi:
10.1038/nm1196.
PMID15711557.
S2CID12338548.
Sakamuro, D; Elliott, KJ; Wechsler-Reya, R; Prendergast, GC (1996). "BIN1 is a novel MYC-interacting protein with features of a tumour suppressor". Nature Genetics. 14 (1): 69–77.
doi:
10.1038/ng0996-69.
PMID8782822.
S2CID21484402.
Prendergast GC, editor (2004). Molecular Cancer Therapeutics: Strategies for Drug Discovery and Development. New York: John Wiley & Sons.
ISBN9780471656166. Reviewed in New England Journal of Medicine 352, 422-423 [2005][23]
Prendergast GC and Jaffee EM, editors (2007). Cancer Immunotherapy: Immune Suppression and Tumor Growth. 1st ed. New York:
Academic Press.
ISBN9780123725516. Reviewed in New England Journal of Medicine 358, 1764-1765 [2008] [24]
Prendergast GC and Jaffee EM, editors (2013). Cancer Immunotherapy: Immune Suppression and Tumor Growth. 2nd ed. New York: Elsevier/Academic Press.
ISBN9780123946331.