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BIOGRAPHY
Dr. Richard George Pestell
Dr. Richard George Pestell, M.B. B.S., M.D., Ph.D., F.R.A.C.P., is the Director, Lombardi Cancer Center, Georgetown University, Washington, DC Francis L. and Charlotte Gragnani Chair, and Chairman of the Department of Oncology, Professor of Oncology and Medicine Georgetown University Medical Center, Washington, DC. Dr Pestell has served as a clinician for over 20 years with clinical training in Oncology and Endocrinology. He serves on a number of regional, national and international governing boards for cancer research, education and treatment, including Medstar Health, NIH, the Raine and the Welcome foundation. Dr. Pestell has been a reviewer for 18 distinct scientific journals and is currently an active editorial board member of 5 journals, including J BioI. Chem., Cancer Res., and Int. J. of Oncology. He has received awards for research (elected member (ASCI), Irma T. Hirschl Weil Caulier Career Scientist Award, Diane Belfer Faculty Scholar), and minority education (Robert Wood Johnson minority medical education).
Dr. Pestell has authored over 170 original publications and book chapters and over 130 published abstracts. His papers have been published in outstanding journals including Cell, Science, Nature Medicine, Molecular Cell and EMBO J. His total scientific impact is over 800. His work is highly cited and he was ranked first in the world for increase in total scientific impact in Biology and first in the world for Biochemistry (ISI) in March 2002. Dr Pestell is funded as the Principal Investigator of 4 R01 grants and PI of the Lombardi Cancer Center CCSG grant.
Dr. Pestell has made major contributions to the area of cell-cycle control. These include the discovery that cyclins are direct transcriptional targets of oncogenic and tumor suppressor signals and that cyclin expression is rate-limiting for oncogene-induced tumor growth in vivo His laboratory established this as a general mechanisms of oncogenic signaling and showed that the cyclins physically interact with nuclear receptors and tumor suppressors providing novel targets for cancer therapies. Most recently he has shown that nuclear receptors are acetylated, and that this event is rate-limiting in hormone signaling and growth control. He demonstrated that this was a general mechanism conserved among nuclear receptors that affect diverse biological processes. His laboratory pioneered the application of tissue-specific inducible transgenics and the development of gene-targeted and transgenic mice to model the role of cell-cycle proteins in human cancer.
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Copyright © 2008 The International Network For Cancer Treatment and Research
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