James A. DeCaprio, M.D.

Associate Professor, Department of Medicine, Harvard Medical School

Discovery Leader, Center for Applied Cancer Sciences, Dana-Farber Cancer Institute

Active Staff and Clinical Associate in Medicine, Medical Oncology, Dana-Farber Cancer Institute

Senior Director, DF/HCC Monoclonal Antibody Core, Dana-Farber Cancer Institute

Associate Professor of Medicine, Medical Oncology, Dana-Farber Cancer Institute

Active Staff and Associate Physician, Medicine, Brigham And Women's Hospital

Contact Info

James DeCaprio
Dana-Farber Cancer Institute
44 Binney Street
Boston, MA, 02115
Mailstop: Mayer 457
Phone: 617-632-3825
Fax: 617-582-8601
james_decaprio@dfci.harvard.edu

Assistant

Tracy Baker
Medical Oncology
Dana-Farber Cancer Institute
Mailstop: DFCI MA440
Phone: 617-582-8605
Fax: 617-582-8601
tracy_baker@dfci.harvard.edu

DF/HCC Program Affiliation

Cancer Cell Biology
Cancer Genetics

DF/HCC Associations

Director, Monoclonal Antibody
Member, Center Scientific Council

Research Abstract

This laboratory is focused on understanding the mechanisms of cellular transformation. In particular, we study how SV40 large T antigen (T Ag) is capable of inducing all of the cellular changes associated with oncogenic transformation. Cellular transformation by T Ag is dependent, at least in part, on inactivation of cellular tumor suppressers. Genetic analysis has led to identification of three transforming domains of T Ag: a C-terminal domain that binds the p53 tumor suppresser and the p300/CBP transcription coactivators; the LxCxE domain that binds the retinoblastoma (pRB) family of tumor suppressers, including pRB, p107 and p130 and an N-terminal domain that resembles the J domain found in the DnaJ/hsp40 family of molecular chaperones. The laboratory seeks to identify novel cellular targets of SV40 T Ag. We have identified a novel E3 ubiquitin ligase, CUL7/FBXW8, that binds to T Ag and appears to contribute to viral oncogenesis.

Publications