Jan Breslow
Jan Leslie Breslow is an American physician and medical researcher who studies atherosclerosis. As of 2017, he is Frederick Henry Leonhardt Professor at Rockefeller University and directs the university's Laboratory of Biochemical Genetics and Metabolism.
Biography
Breslow attended Columbia College, Columbia University, gaining AB and MA degrees in chemistry. He then studied at Harvard Medical School, receiving his MD in 1968. He worked in pediatric medicine at the Boston Children's Hospital and then held a post-doctoral position at the National Heart, Lung, and Blood Institute.In 1973, he took up a post as head of the metabolism division of Boston Children's Hospital, as well as successively instructor, assistant and associate professor in pediatric medicine at Harvard Medical School. In 1984, he moved to Rockefeller University as a professor, and in 1986, was appointed Frederick Henry Leonhardt Professor at the Laboratory of Biochemical Genetics and Metabolism. In 2014, he was appointed director of the university's Sackler Center for Biomedicine and Nutrition. He also works at Rockefeller University Hospital as a senior physician and was physician-in-chief in the 1990s.
Research
Breslow's research has focused on the genetic factors that govern an individual's predisposition to develop atherosclerosis. He started to work on the genetics of cholesterol handling in the late 1970s, and in the early 1980s, with Vassilis Zannis, he was one of the earliest to dissect the different variants of human apolipoprotein E, a component of very low-density lipoprotein. People with different ApoE variants are now known to have different risks not only of heart disease but also of Alzheimer's disease. In 1992, his group found that deleting the mouse gene for ApoE caused the animals to develop elevated blood cholesterol levels and atherosclerosis within around 6 months, on a normal diet. Nobuyo Maeda's group at the University of North Carolina at Chapel Hill also independently created ApoE knockouts that developed atherosclerosis at the same time. The ApoE knockout was the earliest mouse model of the disease, and has been widely used in atherosclerosis research.His group has subsequently researched other genes associated with atherosclerosis, and for example, in 2003, were among the first to identify and characterize PCSK9, which encodes an enzyme acting in a novel cholesterol regulatory pathway. Antibodies targeting PCSK9 were approved by the US FDA as a novel class of cholesterol-lowering drugs in 2015.