Chen Yan, Ph.D.

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Contact

University of Rochester
School of Medicine and Dentistry
601 Elmwood Ave, ACVRI-211 Bailey Road
Rochester, New York 14642

Office: 585 276-9792 (primary)

Lab: 585 276-9843

Fax: 585 276-9830

Portrait

General Research Interests: Regulation and function of cyclic nucleotide phosphodiesterases in the cardiovascular system. Second messenger cyclic nucleotides (cAMP and cGMP) regulate many signaling pathways in the cardiovascular system. For example, the vascular tone, smooth muscle cell growth, and cardiac muscle contractility are all regulated by cyclic nucleotide signaling. We are interested in phosphodiesterases (PDEs), the enzymes that break down cyclic nucleotides and thus control the amplitude, duration, and compartmentalization of cyclic nucleotide signaling in the cell. It has become increasingly clear that cyclic nucleotide degradation by PDEs is not a constitutive function of the cell, but rather a highly regulated one controlled by different mechanisms in different physiological and pathological circumstances. PDE regulation and function is further complicated by the fact that there are more than 50 individual PDEs belonging to 11 different PDE families, yet our understanding of the physiological function of each PDE is far from complete. PDEs have been demonstrated to be good pharmacological targets for therapeutic agents due to the presence of multiple structurally different, tissue-specific, differentially regulated, and functionally distinct isozymes. Several drugs, such as Viagra, have been shown to have unique specific effects via selectively inhibit individual PDE isozymes. Our focus has been on determining the regulation and function of individual PDE isozymes in cardiovascular diseases such as hypertension, atherosclerosis, heart failure, and cardiovascular inflammatory diseases. Ongoing and future studies using in vitro and in vivo approaches will focus on the various roles of PDEs in cardiovascular physiology and pathology, which may provide new therapeutic information for tissue specific interventions in cardiovascular diseases.

Current Appointments

Education
Ph.D. Pharmacology University of Washington 1996
MS Genetics Genetic Institute, Fudan University 1986
BS Biochemistry Department of Biology, Fudan University 1983
Post-Doctoral Training & Residency
Division of Cardiology, University of Washington, Seattle, WA, USA Supervisor: Dr. Bradford Berk 1997 - 1998
Department of Pharmacology, University of Washington, Seattle, WA, USA Supervisor: Dr. Joseph Beavo 1996 - 1997

Lab Description

Research * Regulation and function of cyclic nucleotide phosphodiesterases in the cardiovascular system.


Lab Website

http://www.urmc.rochester.edu/cvri/research/yan-lab.cfm


Recent Journal Articles
Showing the 5 most recent journal articles. (49 available)
Ishinaga H; Jono H; Lim JH; Kweon SM; Xu H; Ha UH; Xu H; Koga T; Yan C; Feng XH; Chen LF; Li JD. "TGF-beta induces p65 acetylation to enhance bacteria-induced NF-kappaB activation." The EMBO journal. 2007; 26(4):1150-62. Epub 2007 Feb 01.
Yan C; Ding B; Shishido T; Woo CH; Itoh S; Jeon KI; Liu W; Xu H; McClain C; Molina CA; Blaxall BC; Abe J. "Activation of extracellular signal-regulated kinase 5 reduces cardiac apoptosis and dysfunction via inhibition of a phosphodiesterase 3A/inducible cAMP early repressor feedback loop." Circulation research. 2007; 100(4):510-9. Epub 2007 Feb 01.
Yan C; Miller CL; Abe J. "Regulation of phosphodiesterase 3 and inducible cAMP early repressor in the heart." Circulation research. 2007; 100(4):489-501.
Garin G; Abe J; Mohan A; Lu W; Yan C; Newby AC; Rhaman A; Berk BC. "Flow antagonizes TNF-alpha signaling in endothelial cells by inhibiting caspase-dependent PKC zeta processing." Circulation research. 2007; 101(1):97-105. Epub 2007 May 24.
Chen C; Korshunov VA; Massett MP; Yan C; Berk BC. "Impaired vasorelaxation in inbred mice is associated with alterations in both nitric oxide and super oxide pathways." Journal of vascular research. 2007; 44(6):504-12. Epub 2007 Jul 30.