CHIRONIAN 2020
BOARD OF TRUSTEES Joseph D. Mark, Chair Joseph Schwartz, M.D., Vice Chair Alan Kadish, M.D. Robert Alter, M.D. Gary Barnett Howard Baruch, M.D. Ben Chouake, M.D. Dee DelBello Rabbi Menachem Genack Gary Gettenberg, M.D. β83 Munr Kazmir, M.D. Moshe Lichtenstein
Stephen Nicholas, M.D. β86 Martin Oliner, Esq. Eliot Peyser Ronald F. Poe Joseph Popack Avi Retter, M.D. Stephen Rosenberg Alan B. Rosenthal, D.M.D. Henry Saphier, M.D. β61 Kenneth R. Theobalds
SCHOOL OF MEDICINE ALUMNI ASSOCIATION BOARD OF GOVERNORS Joseph L. Giamelli, M.D. β02 President
Jerry A. Rubano, M.D. β09 Secretary
John M. Cosgrove, M.D. β83 President-Elect
Damon A. DelBello, M.D. β88 Treasurer
Jay D. Tartell, M.D. β82 Vice President and Archivist
Charles W. Episalla, M.D. β88, M.S. β87 Immediate Past President
Michael A. Antonelle, M.D. β62 Peter E. Bentivegna, M.D. β85 Eileen M. Dieck, M.D. β86 Joseph F. Dursi, M.D. β59 Robert J. Furey, M.D. β62
Jay Y. Lee, M.D. β86 Adelaide G. Nardone, M.D. β83 Christopher F. X. Riegler, M.D. β88 Henry I. Saphier, M.D. β61 Alyssa M. Simeone M.D. β16
BOARD OF ADVISORS Martin Katzenstein, M.D. β78, Chair Nirmala Akkapeddi, M.D. Sabra Brock, Ph.D. William J. Camera, C.P.A. Edward Chew, M.D. β03 Steven H. Cho, D.D.S. Eric I. Choe, M.D. β88 Raymond A. Conta, J.D. Noreen Ferrante, M.D. β86 Kathleen Case Finzel, M.D. β87 Moshe E. Hirth, M.D. β88 Moira T. Imperial Howard Jonas Norman L. Maron, M.D. β70 Beth McErlean-Pierce Ruben Medina
Monica Y. Michell, M.D. β82 Leonard J. Newman, M.D. β70 Rebecca B. Newman, M.D. β05 Stuart A. Paris Lawrence Rein Anne Negrin Reis, M.D. β02 Bruce Schanzer William Smith Susan Tierman, M.D. β79 Steven Topfer, D.O. Rajesh Verma, M.D. β93 Anthony Viceroy Vincent J. Vigorita, M.D. β76 Patricia White, M.D. John M. Zimmerman, M.D. β78
SCHOOL OF HEALTH SCIENCES AND PRACTICE ALUMNI LEADERSHIP COUNCIL Christina Damo, M.S. β10, Chair Karel Amaranth, M.P.H. β10 Jillian Annunziata, M.P.H. β15 Linda Assante, M.P.H. β12 Ellen Bloom, M.P.H. β00 Tiffany Channer, M.P.H. β13 Sheila Conklin, M.P.H. β00 Carolyn DeGoria, D.P.T. β13 Nina Luppino, M.P.H. β09 46
C H I R O N I A N 2020
Zachary R. Messer, M.P.H. β15 Fnu Namrata BDS, M.P.H. β18 Jaclyn (Offitto) Rance, M.S. β10 Jesse S. Rosenblatt, M.P.H. β07 Denise Serrano-Eanelli, Dr.Ph. β19, M.P.H, M.S., R.D. Julia Telfer, M.P.H. β15 Jason Tenzer, M.P.H. β04
ALUMNI PROFILE Anton Bennett, Ph.D. β93 Unlocking the Power of PTPs to Regulate Cell Behavior BY KRISTIN BAIRD RATTINI
H
ow do protein-tyrosine phosphatases (PTPs) regulate cell signaling pathways and lead to the development of disease? Those questions drive the work of Anton Bennett, Ph.D. β93, the Dorys McConnell Duberg Professor of Pharmacology and Professor of Comparative Medicine at the Yale School of Medicine. Throughout his tenure at Yale, Dr. Bennett has unlocked just how crucial of a role that PTPs play in cell function. βPTPs are a very highly regulated family of enzymes involved in modifying proteins,β he explains. βThose modifications allow enzymes in our body to be either switched off or switched on, and so PTPs control the ability of a cell to work properly. Understanding how PTPs are involved in switching enzymes on and off can lead us to knowledge about basic cellular functions, but it has also led us to uncover pathways in which these enzymes when dysfunctional can cause human disease. And what weβve been able to do is connect those altered PTP functions to a variety of different human diseases such as obesity, diabetes and cardiovascular disease.β For example, he discovered that a particular PTP known as MAPK phosphatase 1 is overexpressed in individuals with obesity and type 2 diabetes. Using genetic knockout models in mice, Dr. Bennett eliminated the expression of MAPK phosphatase 1 and then fed the mice a high-fat diet. The mice no longer gained weight and their ability to respond to insulin improved significantly. βWeβre now researching how we can target MAPK phosphatase 1 pharmacologically to come up with new therapeutic strategies for obesity and/or type 2 diabetes.β He also discovered that mutations in a PTP known as SHP-2 lead to the activation of pathways in the heart that cause a congenital heart disease called hypertrophic cardiomyopathy, or enlargement of the heart. βBy identifying targets that SHP-2 interacts with, we can work out how to disable SHP-2 aberrant activity during development,β Dr. Bennett says. During his decade as co-director of the Integrative Cell Signaling and Neurobiology of Metabolism Program at Yale, he has assembled a team of 12 faculty investigators from varied backgrounds to work toward a common goal: to understand the underpinnings of metabolism in health and disease. βWeβre able to answer questions in