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Program Director/Principle Investigator (Last, First, Middle): Cheresh, David A. BIOGRAPHICAL SKETCH Provide the following information for the Senior/key personnel and other significant contributors in the order listed on Form Page 2. Follow this format for each person. DO NOT EXCEED FOUR PAGES. NAME POSITION TITLE Cheresh, David A. Professor eRA COMMONS USER NAME (credential, e.g., agency login) CHERESH EDUCATION/TRAINING (Begin with baccalaureate or other initial professional education, such as nursing, include postdoctoral training and residency training if applicable.) DEGREE INSTITUTION AND LOCATION MM/YY FIELD OF STUDY (if applicable) University of Michigan, Ann Arbor, MI University of Miami, Miami, FL University of Miami, Miami, FL B.S. M.S. Ph.D. 1975 1978 1982 Biology Microbiology Immunology A. Personal Statement A major goal of our research is to understand the molecular of pathological neovascularization. We have begun to understand how growth factors such as VEGF and its receptor(s) as well as integrins impact the process of neovascularization. We are interested in how growth factors and integrins regulate vascular cell signals that enable blood vessel growth and stabilization. My research efforts have helped to delineate how these processes are regulated at the molecular level. These studies have lead to the development of integrin antagonists as novel therapeutics for cancer treatment that function to suppress the growth of angiogenic blood vessels. Two drugs that have developed from our work include Vitaxin (Abegrin) a humanized monoclonal antibody that targets avb3 and Cilengitide a cyclic peptide antagonist of integrins avb3 and avb5. Both of these drugs have show clinical activity in cancer patients in Phase II trials and are now being tested in Phase III trials. It is likely that these efforts will help to define the molecular basis of drugs such as Vitaxin and Cilengitide which are beginning to show promise for patients with metastatic disease. A second area of focus involves the development of tumor vascular targeted nanoparticles. We have developed strategies to target drugs, genes and imaging molecules to neovascular tissue. This has allowed us to both image or therapeutically treat the growth of tumors. B. Positions and Honors Positions and Employment 1985-1989 Assistant Professor, Dept. of Immunology, The Scripps Research Institute, La Jolla, CA. 1989-1996 Associate Professor, Dept. of Immunology, The Scripps Research Institute, La Jolla, CA. 1996-2005 Professor, Depts. of IMM & Vascular Biology, The Scripps Research Institute, La Jolla, CA. 2005-present Professor, Department of Pathology, University of California, San Diego, La Jolla, CA. 2005-present Professor, Assoc. Director for Translational Res., Moores UCSD Cancer Center, La Jolla, CA. 2006-present Vice Chair for Research, Dept. of Pathology, UCSD, La Jolla, CA. Other Experience and Professional Memberships 1987-present Member, The American Society for Cell Biology 1994-present Member, American Association for the Advancement of Science 1996-present Scientific Advisory Board member, North American Vascular Biology Organization 1997 Myron Karon Memorial Lecturer, Children’s Hospital, Los Angeles 1997 15th Hans Lindner Memorial Lecturer, Weizmann Institute of Science, Rehovot, Israel 1998-present Member, American Association for Cancer Research 1998 McGill University Visiting Professor in Oncology, Montreal, Quebec, Canada 1998 Robert Bear Lecturer, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada 2000 Chairman, Gordon Research Conference on Vascular Biology PHS 398/2590 (Rev. 06/09) Page 1 Biographical Sketch Format Page Cheresh, David A. 2001 Chairman, Gordon Research Conference on Angiogenesis and Microcirculation 2002 Organizer and Chairman Keystone Symp. on Biological Response to the Extracellular Matrix 2004-present Member, The American Society for Hematology 2004 Visiting Professorship, University New Mexico Cancer Center 2007 Organizer and Chairman Keystone Symp. ”Host Cell Interaction and Response to Cancer Cell” 2008 Organizer and Chairman, 4th Annual Translational Onc. Symp. Moores Cancer Ctr, La Jolla, CA 2009 Organizer and Chairman, 21st Annual Usha Mahajani Symposium, La Jolla, CA 2010 Invited speaker, Gordon Research Conference, University of New England, Biddeford, ME 2010 Invited speaker, 16th International Vascular Biology Meeting, UCLA, Los Angeles, CA Program Director/Principle Investigator (Last, First, Middle): Honors 1999 1999 2002 2003 2003 2005 2006 2007 2007 2007 2007 2009 2010 2010 Recipient, 75th Anniversary Spirit of Scripps Award, La Jolla, California Recipient, NIH MERIT award, CA50286 Keynote Spkr, Society Biological Therapy Understanding Angiogenesis/Molecular Mechanisms Keynote Spkr, Cold Spring Harbor Lab “Vector Targeting Strategies for Therapeutic Gene Del. Keynote Spkr, Medical Univ. SC, Hollings Cancer Center Research Symposium Basic Science Lecture Award, American Society of Cytopathology 53rd Annual Scientific Mtg Elkin Distinguished Lecture, Emory University, Atlanta, Georgia Davis Distinguished Lecturer, Cardiovascular Day 2007, University of Missouri, St. Louis, MO Featured Speaker, Sidney Kimmel Cancer Center symposium. Coronado, CA Highlight Lecture at Vasculata 2007, Chapel Hill, NC Keynote Lecture, 3rd Annual Meeting of the American Academy of Nanomedicine, La Jolla, CA Recipient, NIH MERIT award, CA50286 Recipient, Paget-Ewing award of the Metastasis Research Society and AACR Meeting Keynote Lecture, 4th Mayo Clinic Angiogenesis Symposium, Mackinac Island, MI C. Selected Peer-reviewed Publications (Selected from 214 peer-reviewed publications) Recent publications of importance to the field (in chronological order) 1. Hood, J.D, Bednarski, M, Frausto, R, Guccione, S, Reisfeld, R.A, Xiang, R. & Cheresh D.A. Tumor regression by targeted gene delivery to the neovasculature. Science 2002; 296:2404-7. 2. Alavi, A, Hood, J.D, Frausto, R, Stupack, D.G. & Cheresh D.A. Role of Raf in vascular protection from distinct apoptotic stimuli. Science 2003; 301:94-6. 3. Hood, J.D, Frausto, R, Kiosses, W.B, Schwartz, M.A. & Cheresh D.A. Differential v-integrin-mediated Ras-ERK signaling during two pathways of angiogenesis. J Cell Biol 2003; 162(5): 933-43. PMCID:PMC2172815. 4. Weis, S.M. & Cheresh D.A. Pathophysiological consequences of VEGF-induced vascular permeability. Nature 2005; 437:497-504. 5. Stupack, D.G, Teitz, T, Potter, M, Mikolon, D, Kidd, V.J, Lahti, J.M. & Cheresh D.A. Potentiation of neuroblastoma metastasis by loss of caspase 8. Nature 2006; 439:95-9. 6. Alavi, A.S, Acevedo, L, Min, W. & Cheresh D.A. Chemoresistance of endothelial cells induced by bFGF depends on Raf-1-mediated inhibition of the pro-apoptotic kinase, ASK1. Cancer Res 2007; 67:2766-72. 7. Murphy, E.A, Majeti, B.K, Barnes, L, Makale, M, Weis, S.M, Wrasidlo, W. & Cheresh D.A. Nanoparticlemediated drug delivery to tumor vasculature suppresses metastasis. PNAS 2008; 105:9343-8. PMCID2453735. 8. Stockmann, C, Doedens, A, Weidemann, A, Zhang, N, Takeda, N, Greenberg, J.I, Cheresh D.A. and Johnson, R.S. Deletion of vascular endothelial growth factor in myeloid cells accelerates tumorigenesis. Nature 2008; 456: 814-9. 9. Greenberg, J.I, Shields, D.J, Barillas, S.G, Acevedo, L.M, Murphy, E, Huang, J, Scheppke, E, Stockmann, C, Johnson, R.S, Angle, N. & Cheresh D.A. A role for VEGF as a negative regulator of pericyte function and vessel maturation. Nature 2008; 456: 809-13. PMCID2605188. PHS 398/2590 (Rev. 06/09) Page 2 Continuation Format Page Program Director/Principle Investigator (Last, First, Middle): Cheresh, David A. 10. Ricono, J.M, Huang, M, Barnes, L.A, Lau, S.K, Weis, S.M, Schlaepfer, D.D, Hanks, S.K. & Cheresh D.A. Specific crosstalk between EGFR and integrin αvβ5 promotes carcinoma cell invasion and metastasis. Can Res 2009; 69(4): 1383-91. PMCID2741736. 11. Desgrosellier, J.S, Barnes, L.A, Shields, D.J, Huang, M, Lau, S.K, Prévost, N, Tarin, D, Shattil, S.J. and Cheresh D.A. Integrin avb3/c-src “Oncogenic Unit” Promotes Anchorage-independence and Tumor Progression. Nature Medicine 2009; 15:1163-1169. PMCID2759406 12. Desgrosellier, J.S. & Cheresh, D.A. Integrins in Cancer: Biological Implications and Therapeutic Opportunities. Nat Rev Cancer 2010 Jan; 10(1):9-22. PMCID-in process. 13. Shields, D.J, Niessen, S, Murphy, E, Mielgo, A, Desgrosellier, J.S, Lau, S.K, Barnes, L.A, Lesperance, J, Bouvet, M, Tarin, D, Cravatt, B.F, & Cheresh D.A. RBBP9: A tumor-associated serine hydrolase activity required for pancreatic neoplasia. Proc Natl Acad Sci USA. 2010 Feb 2; 107(5):2189-94. PMCID2836678 14. Murphy, E.A, Shields, D.J, Stoletov, K, Dneprovskaia, E, McElroy, M, Lindquist,J, Acevedo, L, Anand, S, Majeti, B.K, Tsigelny, I, Saldanha, A, Walsh, B, Hoffman, R.M, Bouvet, M, Klemke, R, Vogt, P.K, Arnold, L, Wrasidlo, W. & Cheresh D.A. Disruption of angiogenesis and tumor growth with an orally active drug that stabilizes the inactive state of PDGFRβ/B-RAF. Proc Natl Acad Sci USA. 2010 Mar 2:107(9):4299-304. PMCID2840076 15. Anand, S, Majeti, B.K, Acevedo, L.M, Murphy, E.A, Mukthavaram, R, Scheppke, L, Huang, M, Shields, D.J, Lindquist, J.N, Lapinski, P.E, King, P.D, Weis, S.M. and Cheresh, D. A. MicroRNA-132 mediated loss of p120RasGAP activates endothelium to facilitate pathological angiogenesis. Nature Medicine. 2010, 16:909-14. PMCID-in process. D. Research Support: Ongoing Research Support: R01 CA045726 Cheresh (PI) 04/01/07 - 05/31/12 Regulation of metastasis by alpha V integrin and Src The major goals of this application will determine how EGFR and Src influence in metastatic pancreatic cancer. Role: PI R01 CA095262 Cheresh (PI) 08/01/07 - 05/31/12 Regulation of cell invasion by apoptotic mechanisms The overall goal of this grant is to characterize mechanisms of cell survival/death among invasive cells. Role: PI P30 CA 023100 Carson (PI) 07/01/96 - 04/30/12 Cancer Center Support Grant (CCSG) This grant provides infrastructure and developmental funds support of the Moores UCSD Cancer Center, an NCI designated comprehensive cancer center. The Center has 7 research programs, 11 shared resources and developmental programs organized to foster and promote collaboration and translation of discovery into advanced patient care toward the ultimate control of cancer. Role: Co-Investigator R37 CA050286 Cheresh (PI) 05/01/09 - 03/31/14 VEGF and PDGF in Angiogenesis and Tumor Progression The goals of this grant are to understand how PDGF and VEGF regulate blood vessel maturation and thereby contribute to growth and invasion of tumors. Role: PI P01 HL057900 Shattil (PI) 02/01/08 - 03/31/13 Integrin Signaling in Hemostasis and Blood Diseases This project will elucidate the pathways that regulate and coordinate migration of vascular cells. Role: Co-Investigator PHS 398/2590 (Rev. 06/09) Page 3 Continuation Format Page Program Director/Principle Investigator (Last, First, Middle): Cheresh, David A. P01 CA104898 Talamini (PI) 05/01/05 - 08/30/11 Targeting Vessels in Tumors This project is designed to complement the other projects in this program by providing a gene delivery platform to test new targets and strategies to disrupt the tumor vasculature and thereby influence the growth and metastasis of human cancer. Role: Co-Investigator R01 CA045726 Cheresh (PI) 07/01/09 - 06/30/11 Regulation of metastasis by alpha V integrin and Src The goal of this proposal is to combine respective areas of expertise in advanced functional proteomics and invivo tumor biology models to identify and validate novel therapeutic targets of pancreatic tumor metastasis. Role: PI Completed Research Support: R21 CA129660 Cheresh (PI) 09/01/07 - 08/31/09 Identification of novel pancreatic cancer biomarkers The goals are to enable detection of pancreatic cancer at the earliest stages and identify novel predictive markers of disease using a cross-species advanced proteomics approach. Role: PI R01 HL78912 Cheresh (PI) 08/01/05 - 07/31/10 Endothelial Barrier Function Regulation by VEGF The objective of this grant is to understand, at the molecular and biological levels, how endothelial cell (EC) barrier function is modulated in blood vessels exposed to vascular endothelial cell growth factor (VEGF), and to determine the consequences of this process in disease. Role: PI U54 CA119335 Esener (PI) 09/01/05 - 08/31/10 Center of Nanotechnology for Treatment, Understanding, and Monitoring of Cancer The objective of this proposal is to establish a role for nanotechnology as a viable therapeutic option for cancer patients. We will work with chemists and biologists to develop novel nano-platforms for tumor-targeted delivery of drugs. Role: Co-Investigator PHS 398/2590 (Rev. 06/09) Page 4 Continuation Format Page