In this article, we are going to explore Napoleone Ferrara and everything it has to offer. From its origins to its impact on today's society, we will dive into a comprehensive analysis of Napoleone Ferrara and its relevance in different aspects of life. We will discover how Napoleone Ferrara has evolved over time and how it has left a mark on history. Additionally, we will examine how Napoleone Ferrara has changed the way people interact and relate to each other. This article seeks to provide a comprehensive view of Napoleone Ferrara and its influence in today's world. Get ready to immerse yourself in the fascinating world of Napoleone Ferrara!
Napoleone Ferrara (born 26 July 1956 in Catania) is an Italian-American molecular biologist who joined University of California, San DiegoMoores Cancer Center in 2013 after a career in Northern California at the biotechnology giant Genentech, where he pioneered the development of new treatments for angiogenic diseases such as cancer, age-related macular degeneration (AMD), and diabetic retinopathy.[1] At Genentech, he discovered VEGF—and made the first anti-VEGF antibody—which suppresses growth of a variety of tumors. These findings helped lead to development of the first clinically available angiogenesis inhibitor, bevacizumab (Avastin), which prevents the growth of new blood vessels into a solid tumor and which has become part of standard treatment for a variety of cancers.[citation needed] Ferrara's work led also to the development of ranibizumab (Lucentis), a drug that is highly effective at preventing vision loss in intraocular neovascular disorders.[citation needed]
At UC San Diego Moores Cancer Center, Ferrara, a member of the National Academy of Sciences since 2006, serves as Senior Deputy Director for Basic Science and is a Distinguished Professor of Pathology in the UC San Diego School of Medicine, where he will continue cancer drug research targeting angiogenesis.[citation needed] He is presently focusing on investigating mechanisms of tumor angiogenesis alternative to VEGF, in particular the role of factors produced by myeloid cells and fibroblasts in mediating resistance to VEGF inhibitors.[citation needed]