George C. Prendergast, PhD

Photo of George Prendergast


Phone: 484.476.8144

Fax: 484.476.8533

Office: L48

Department: Administration

Association: Resident Faculty

Other Appointment:Professor


  • BA, Biochemistry, University of Pennsylvania, 1983
  • MS, Molecular Biophysics, Yale University, 1984
  • PhD, Molecular Biology, Princeton University, 1989


  • 2004 - Professor, President & CEO, Lankenau Institute for Medical Research
  • 2006 - Professor, Dept. of Pathology, Anatomy & Cell Biology, Jefferson Medical School, Thomas Jefferson University
  • 2006 - Co-Director, Program in Cell Biology & Signaling, Kimmel Cancer Center, Thomas Jefferson University
  • 2007 - CEO, LIMR Development, Inc.
  • 2010 - Editor-in-Chief, Cancer Research

Research Interests

Lab Personnel

  • James DuHadaway, Research Lab Associate
  • Sunil Thomas, PhD, Research Assistant Professor
  • U. Margaretha Wallon, PhD, Research Assistant Professor

Selected Awards and Honors

  • 1995 - American Cancer Society Junior Faculty Award
  • 1995 - Pew Scholar in the Biomedical Sciences Award
  • 2000 - Who's Who in America
  • 2003 - Highlighted Project, 2003 DoD Prostate Cancer Research Program Report
  • 2008 - Special Achievement Award, Chinese Society for Clinical Oncology
  • 2008 - Designated One of the 250 Historically Most Influential Alumni of Princeton University
  • 2011 - Translational Medicine Award, Shanghai Translational Medicine Forum, Shanghai China
  • 2011, 2014 - Highlighted ‘In the Pipeline’ Project, DoD Breast Cancer Research Program Annual Report
  • 2011 - European Academy of Tumor Immunology 
  • 2012 - Inventor of the Year, Jefferson Kimmel Cancer Center

Lay Description

By studying disease modifier genes we seek to develop new principles to treat cancer, diabetes, autoimmune disorders and cardiovascular disease. Currently most biomedical research focuses on understanding disease pathways. We seek to understand general disease modifier pathways that determine disease severity, an understudied area from which many useful drugs such as NSAIDs and statins are based. A major thrust of our present work focuses on modifiers of inflammatory processes which contribute significantly to the severity of many age-associated diseases. In our main project, we have developed a new class of drugs that recruit the immune system to eradicate a broad spectrum of advanced cancers, including breast, lung, skin, and pancreas tumors that are often refractory to chemotherapy. These drugs, called IDO inhibitors, are presently in Phase II clinical trials. In other projects, with our Lankenau colleagues we are developing new agents to treat autoimmune disorders, reduce risks of cardiovascular disease, and ameliorate diabetes.

Scientific Description

Our laboratory is interested primarily in cancer genes, cancer immunology and molecular therapeutics. We use transgenic mouse models and preclinical drug strategies to learn new ways to suppress cancer, focusing on long-term goals of improving strategies for cancer prognosis and treatment.

Localized tumors are often curable if they are detected before progression to invasive status, but many patients diagnosed with cancer already have invasive disease. What factors dictate malignant progression and how might they be therapeutically exploited? Molecular therapeutics that target key oncogene and tumor suppressor pathways show some clinical promise, but they have shown limited efficacy to date. Cancer modifier pathways that influence the immune microenvironment of tumor cells may strongly influence clinical course. Accordingly, new therapies we are developing are based on blocking enzymes that limit the ability of immune cells to destroy cancer cells or drive disease.

RhoB studies derive from our long-standing research on this member of the Ras/Rho superfamily in cancer cell signaling. Recent work in collaboration with Drs. Lisa Laury-Kleintop and Laura Mandik-Nayak at Lankenau has opened exciting new directions in studies of the role of RhoB in autoimmune and cardiovascular disease. A start-up company has been created to fund and advance the preclinical and clinical work needed to explore a provocative new therapy emerging from these novel directions, which in principle may be useful to treat one or more diseases in important areas of medicine.

Bin1 studies originating in cancer cell studies led us to discover that it regulates the immune modulatory enzyme indoleamine 2,3-dioxygenase (IDO). Bin1 modifies inflammation in a variety of settings including cancer. Recently, in preclinical studies we found that its genetic blockade can limit the development of inflammatory bowel disease (colitis). Based on this finding, we are now investigating the use of Bin1 antibodies we have developed to treat this disorder.

IDO is a tryptophan catabolic enzyme that blocks T cell activation in physiological settings such as pregnancy and in many pathophysiological settings like cancer. IDO is very widely activated as a mechanism of immune escape by cancer cells. Genetic studies reveal that IDO is essential for inflammation-driven cancers, not only supporting immune escape but also angiogenesis and metastasis. We pioneered preclinical studies of IDO inhibitory drugs that can arrest tumor growth and enhance chemotherapeutic efficacy. Mechanistic studies of one clinical lead inhibitor, D-1MT (indoximod), will greatly assist ongoing Phase II studies of this drug. Translational studies including on an IDO-related gene called IDO2 discovered at Lankenau are currently a major focus of the laboratory.

Dr. Prendergast's Google Scholar page

2015 Selected Publications

Novel Colitis Immunotherapy Targets Bin1 and Improves Colon Cell Barrier Function. Thomas S, Mercado JM, DuHadaway J, DiGuilio K, Mullin JM, Prendergast GC. Dig Dis Sci. 2015 Jul 21.

Cardiac-Specific Disruption of Bin1 in Mice Enables a Model of Stress- and Age-Associated Dilated Cardiomyopathy. Laury-Kleintop LD, Mulgrew JR, Heletz I, Nedelcoviciu RA, Chang MY, Harris DM, Koch WJ, Schneider MD, Muller AJ, Prendergast GC. J Cell Biochem. 2015 Nov;116(11):2541-51.

Accumulation of an endogenous tryptophan-derived metabolite in colorectal and breast cancers. Puccetti P, Fallarino F, Italiano A, Soubeyran I, MacGrogan G, Debled M, Velasco V, Bodet D, Eimer S, Veldhoen M, Prendergast GC, Platten M, Bessede A, Guillemin GJ. PLoS One. 2015 Apr 16;10(4):e0122046.

Cardiac-Specific Disruption of Bin1 in Mice Enables a Model of Stress- and Age-Associated Dilated Cardiomyopathy. Laury-Kleintop LD, Mulgrew JR, Heletz I, Nedelcoviciu RA, Chang MY, Harris DM, Koch WJ, Schneider MD, Muller AJ, Prendergast GC. J Cell Biochem. 2015 Nov;116(11):2541-51.

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