Subspecialty	Gastroenterology
Clinical Interests	Liver Disease
	Gastroenterology
Languages	English
Gender	Male
E-mail	scott.friedman@mssm.edu
Education and Training	MD, Mount Sinai School of Medicine
	Residency, Internal Medicine, Beth Israel Hospital
	Residency, Internal Medicine, Beth Israel Hospital
	Fellowship, Gastroenterology, University of California Hospitals
Awards	New award
	2009 President American Assn for the Study of Liver Diseases
	2008 Sackler Distinguished Lectureship Tel Aviv University, Israel
	2008 Dean's Distinguished Lecturer Georgetown U. School of Medicine
	2008 Fellow of the American Gastroenterological Assn
	2008 Advisory Council Natl Institute on Alcohol Abuse and Alcoholism
	2007 America's Top Doctors
	2006 Solomon Berson Dept of Medicine Housestaff Teaching Award
	2005 John Carbone Visiting Professor Medicine, NY, NY
	2004 Lieberman Memorial Lecture Lenox Hill Hospital Dept of Medicine, NY, NY
	2004 International Hans Popper Award to Outstanding Researcher in Hepatology
	2003 CecilWatson Lecturer U. Minnesota
	2003 International Hans Popper Award to Outstanding Researcher in Hepatology
	2001 Jacobson Visiting Professor and Lecturer U. of Newcastle School of Medicine
	1999 Ernest Hafter Memorial Lecture Swiss Gastroenterological Association
	1999 Charles Flood Memorial Lecture NY Cornell Presbyterian Hosp. GI Division
	1998 Irene and Dr. Arthur Fishberg Professor of Medicine Mount Sinai School of Medicine
	1995 Fulbright Senior Scholar Award
	1993 Saul Horowitz Outstanding Alumnus Award Mount Sinai School of Medicine
	1992 'Bay Area's Best Doctors' San Francisco Focus Magazine
	1979 Chapter President Alpha Omega Alpha, Lambda Chapter
	1979 Arthur H. Aufses Sr., Prize in Surgery Mount Sinai School of Medicine
	1976 Cum Laude Rensselaer Polytechnic Institute

Dr. Friedman has performed pioneering research into the underlying causes of scarring, or fibrosis associated with chronic liver disease, which affects millions worldwide. Dr. Friedman was the first to isolate and characterize the hepatic stellate cell, which is the key cell type responsible for scar production in liver. This work followed from earlier studies by Drs. Hans Popper and Fenton Schaffner of Mount Sinai who emphasized the stellate cell's potential importance in liver disease. Liver fibrosis has assumed major importance as a potential treatment target for the millions of patients infected with Hepatitis C, and much of this excitement can be traced to Dr. Friedman's contributions. His work has been continuously funded by the NIH since 1985, in addition to grants from American Heart Association and the American Gastroenterological Association.

Dr. Friedman is a 1979 graduate of Mount Sinai School of Medicine, where he served as the President of Alpha Omega Alpha Honor Society and was an awardee of the Arthur Aufses, Sr. Prize in Surgery. After graduation Dr. Friedman was a Medical Resident at the Beth Israel Hospital, Harvard Medical School, Boston, then a Gastroenterology Fellow at UCSF before assuming a faculty position there which he held for ten years. During a 1995-96 sabbatical from UCSF he was a Fulbright Scholar and Visiting Professor at the Weizmann Institute of Science in Israel, in the laboratory of Dr. Moshe Oren. In 2003 Dr. Friedman was awarded the Hans Popper International Liver Research Prize, recognizing his pioneering work into mechanisms and treatments of hepatic fibrosis.

Dr. Friedman has given invited lectures throughout the world and is also a respected author. His 1993 'Seminars in Medicine' article on liver fibrosis in the New England Journal of Medicine is the most widely cited review on the topic. He has mentored 10 postdoctoral fellows and students all of whom remain in academic training programs or faculty.

In addition to his laboratory research, Dr. Friedman is a respected clinician and teacher, having been listed among the 'Bay Area's Best Doctors' by San Francisco Focus Magazine. He maintains a clinical practice in Liver Diseases at Mount Sinai.

Dr. Friedman is currently an Associate Editor of Hepatology, and on the Editorial Board of Journal of Gastroenterology and Hepatology. He is co-Editor of the textbook 'Current Diagnosis and Treatment in Gastroenterology'. He is on the Scientific Advisory Board of the US-Israel Binational Science Foundation. Dr. Friedman was a recipient in 1993 of the Saul Horowitz, Jr. Outstanding Alumnus Award from Mount Sinai and is a member of the American Society of Clinical Investigation since 1995. He serves on numerous committees for the American Association for the Study of Liver Diseases and the American Gastroenterological Association.

Fibrosis Research Center
Mount Sinai Alcoholic Liver Disease Research Center

Curriculum Vitae: Curriculum Vitae

Education and Training	MD, Mount Sinai School of Medicine
	Residency, Internal Medicine, Beth Israel Hospital
	Residency, Internal Medicine, Beth Israel Hospital
	Fellowship, Gastroenterology, University of California Hospitals
Board Certification	Gastroenterology

Subspecialty	Gastroenterology
Clinical Interests	Liver Disease
	Gastroenterology
Languages	English
Board Certification	Gastroenterology

Dr. Friedman is the Director of both the Fibrosis Research Center and the Mount Sinai Alcoholic Liver Disease Research Center.

Specific Clinical/Research Interest:
1) Role of KLF6 tumor suppressor gene in cancer pathogenesis;
2) Molecular regulation of hepatic fibrosis;
3) Testing of novel antifibrotic therapies in preclinical models and human trials

Current Students: MD/PhD: Ursula Lang, Zhara Ghiassi-Nejad, Yedidya Saiman (co-mentor); Ph.D. - Jingjing Jiao (co-mentor_; Doris Duke Medical Student Research Fellow: Andrew Paris

Postdoctoral Fellows: Lars Bechmann, M.D.; Beatriz Minguez, M.D.; Sara Tofannin, Ph.D.; Rebekka Hannivoort, M.D.; Ursula Munoz, PhD; Diana Vetter M.D.

Research Personnel: Johnny Loke, M.S. (Lab Manager); Feng Hong M.D.

Summary of Research Studies:
-Role of KLF6 in Cell Growth and Human Cancer.

We have cloned a novel Kruppel like factor, KLF6, from liver that is ubiquitously expressed, and mutated in a number of human cancers. Major KLF6-related research projects are:

-Identification of KLF6 transcriptional targets by array
-Role of KLF6 in liver development
-Inactivation of KLF6 in human cancers, esp. hepatocellular carcinoma
-Animal models of cancer with KLF6 dysregulation
-KLF6 Interacting proteins
-Animal models of KLF6 dysregulation (tissue specific KO; KLF6 +/- mice responses to injury and carcinogens) Molecular Regulation of Hepatic Fibrosis.

Our work explores the molecular mechanisms of wound healing and fibrosis in liver. We use a variety of animal and cell culture models to identify key inflammatory mediatiors and signaling molecules regulating the activation of hepatic stellate cells, the principle fibrogenic cells in liver. Additionally, we test candidate antifibrotic lead compounds to develop potential new therapies for patients with chronic fibrosing liver diseases. Specific projects include:

-Testing of antifibrotic lead compounds in animal models
-Clinical trials of antifibrotic therapies in patients with chronic liver disease
-Exploration of mechanisms underlying risk-associated genes in hepatic fibrosis
-Role of KLF6 splicing in hepatic stellate cell activation

Guo J, Loke J, Zheng F, Hong F, Yea S, Fugita M, Tarocchi M, Abar OT, Huang H, Sninsky JJ, Friedman SL. Functional linkage of cirrhosis-predictive single nucleotide polymorphisms of toll-like receptor 4 to hepatic stellate cell responses. Hepatology 2009;.

Friedman SL. Hepatic stellate cells: protean, multifunctional and enigmatic cells of the liver. Physiological reviews 2008; 88: 125-172.

Hoshida Y, Augusto A, Kobayashi M, Peix J, Chiang D, Camargo A, Gupta S, Moore J, Wrobel MJ, Lerner J, Reich M, Chan JA, Glickman JN, Ikeda K, Hashimoto M, Watanabe G, Roayaie S, Schwartz M, Thung S, Salvesen HB, Mazzaferro GS V, Bruix J, Friedman SL, Kumada H, Llovet JM, Golub TR. Gene expression profiles of adjacent liver predict outcome in hepatocellular carcinoma. New England J Med 1995-2004, 2008; 359(19).

Friedman SL. Mechanisms of hepatic fibrosis. Gastroenterology 2008 May; 134(6): 1655-1669.

Yea S, Narla G, Zhao X, Garg R, Tal-Kremer S, Hod H, Villanueva A, Loke J, Tarocchi M, Akita K, Shirasawa S, Sasazuki T, Martignetti JA, Llovet JM, Friedman SL. Ras promotes growth by alternative splicing-mediated inactivation of the KLF6 tumor suppressor in hepatocellular carcinoma. Gastroenterology 2008; 134(5): 1521-1531.

Friedman SL. News & Views: Targeting siRNA to arrest fibrosis. Nature Biotechnology 2008; 26(4): 399-400.

Friedman SL, Nieto N. Preview. Cannabinoids provoke alcoholic steatosis through a conspiracy of neighbors. Cell Metabolism 2008; 7(3): 187-188.

Hartel M, Narla G, Wente MN, Nathalia A, Giese NA, Martignoni ME, Martignetti JA, Friess H, Friedman SL. Increased alternative splicing of the KLF6 tumor suppressor gene correlates with prognosis and tumor grade in patients with pancreatic cancer. European J Cancer 2008; 44(13): 1895-1903.

Kremer-Tal , Narla G, Chen Y, Hod E, DiFeo A, Yea S, Lee JS, Schwartz M, Thung SN, Fiel IM, Banck M, Zimran , Thorgeirsson SS, Mazzaferro V, Bruix J, Martignetti JA, Llovet JM, Friedman SL. Downregulation of KLF6 is an early event in hepatocarcinogenesis, and stimulates proliferation while reducing differentiation in vivo. Journal of Hepatology 2007; 46: 645-654.

Narla G, Kremer-Tal S, Matsumoto N, Zhao X, Yao S, Kelley K, Tarocchi M, Friedman SL. In vivo regulation of p21 by the KLF6 tumor suppressor gene in mouse liver and human hepatocellular carcinoma. Oncogene 2007; 26(30): 4428-4434.