|
|
|
Calvin
Vary, Ph.D.
Center for Molecular Medicine
Maine Medical Center Research Institute
81
Research Drive
Scarborough, ME 04704
(207) 885-8148 Office
(207) 885-8175 Lab
(207) 885-8179 Fax
varyc@mmc.org
|
 |
|
Biosketch
Calvin
Vary, Ph.D., is a Senior Scientist and principle investigator
in the Center for Molecular Medicine at MMCRI. Dr. Vary received
his PhD in Biological Chemistry from Michigan
State University. Following work in the area of RNA secondary
structure and its relationship to function, he spent several years
conducting research and development in the biotechnology sector
at Allied Signal Corp. and moved to Maine to join AgriTech, now
IDEXX Corp. He joined the Maine
Cytometry Research Institute in 1991 prior to this Institution's
incorporation into the Maine Medical Center as the MMC Research
Institute. Currently in MMCRI's Center for Molecular Medicine,
Dr. Vary studies the regulation of TGFb
receptor signaling in vascular development and disease. He also
directs the Protein, Nucleic
Acid Analysis and Cell Imaging Core facility within the Center
of Biological Research Excellence in Vascular
Biology.
|
|
Research
Interests
Our
laboratory works to understand how endoglin, a TGFb
receptor-associated transmembrane protein, and the TGFb
receptors, regulate the process of angiogenesis and the occurrance
of vascular pathology. In humans, mutations in the genes encoding
either endoglin, or the TGFb receptor
ALK1, cause the vascular disease hereditary hemorrhagic telangiectasia
(HHT). Currently, we are interested in those aspects of endoglin's
structure that regulate its phosphorylation by the TGFb
receptors, and how endoglin phosphorylation effects cell physiology
within a variety of tissue contexts. Understanding the details
of endoglin's function will lead to mechanistic insights into
the processes of cell adhesion, migration, and invasion, and will
advance our understanding of a variety of complex biological processes,
including vascular development, vascular disease, and cancer progression.
|
|
Educational,
Community, State, and International Affiliations
Dr.
Vary is a long-standing member of the MMC Mentored
Research Committee and has hosted several MMC residents and
fellows in his laboratory. He currently holds the position of
adjunct associate professor at the University
of Southern Maine and in the University
of Vermont College of Medicine. He is an associate of the
Graduate Faculty in the University
of Maine Graduate School of Biomedical Sciences in and the
Functional Genomics
Program. In
addition, Dr. Vary serves as chair of the Maine
Technology Institute Biotechnology Sector Board, and is a
member of the HHT Foundation
International, Global
Research and Medical Advisory Board.
|
|
Current Staff
Diana
Romero, PhD, Postdoctoral Fellow
Aleksandra
Terzic, DVM, PhD, Postdoctoral Fellow
Kira
Young, BS, Doctoral Candidate
and
Barbara Conley, MS, Research Associate.
|
|
Recent Placements
and Graduates
Rosi
Koleva, PhD, Department of Cancer Biology, Dana-Farber Cancer
Institute, Harvard Medical School
Thea
Nicola, MD, PhD, Department of Cell Biology, University of Alabama.
Maria
Mancini, PhD, Department of Pathology, Beth Israel Deaconess Medical
Center
|
|
Selected
Recent Publications
Nikopoulos GN, Martins JF, Adams TL, Karaczyn A, Adams D, Vary
C, Verdi JM. NRAGE: A Potential Rheostat During Branching Morphogenesis.
Mech
Dev 2009; 126:337-349.
Romero,
D, Iglesias, M, Vary, CPH, and Quintanilla, M. Functional blockade
of Smad4 leads to a decrease in b-catenin
levels and signaling activity in human pancreatic carcinoma cells.
Carcinogenesis,
2008; 5:1070-1076.
Craft,
CS, Li, Xu, Romero, D, Vary, CPH, and Bergan, RC. Genistein induces
phenotypic reversion of endoglin deficiency in human prostate
cancer cells. Mol
Pharmacol. 2008;73(1):235-42.
Bernabeu
C, Conley BA, and Vary CPH. Novel Biochemical Pathways of Endoglin
in Vascular Cell Physiology. J.
Cell. Biochem., 2007; 102:1375-1388.
Mancini
ML, Verdi JM, Conley BA, Nicola T, Spicer DB, Oxburgh L, and Vary,
CPH. Endoglin is required for myogenic differentiation potential
of neural crest stem cells. Dev.
Biol. 2007; 308: 520-533.
Craft
CS, Romero D, Vary CPH, and Bergan, RC. Endoglin inhibits prostate
cancer motility via activation of the ALK2-Smad1 pathway. Oncogene,
2007; 26:7240-50.
Santibanez
JF, Letamendia A, Perez-Barriocanal F, Silvestri C, Saura M, Vary
CPH, Lopez-Novoa JM, Attisano L, Bernabeu C. Endoglin increases
eNOS expression by modulating Smad2 protein levels and Smad2-dependent
TGF- signaling. J.
Cell Physiol. 2007; 210:456-468.
Jerkic
M, Rivas-Elena JV, Santibanez JF, Prieto M, Rodríguez-Barbero
A, Pericacho M, Arévalo M, Vary CPH, Letarte M, Bernabeu C, and
López-Novoa JM. Endoglin regulates COX-2 expression and activity.
Circ.
Res. 2006; 99:248-56.
Koleva
RI, Conley BA, Romero D, Riley KS, Marto JA, Lux A, and Vary CPH.
Endoglin Structure and Function: Determinants of Endoglin Phosphorylation
by TGFb Receptors. J.
Biol. Chem. 2006; 281:25110-25123.
Lindner
V, Conley BA, Friesel R, Vary CPH. The role of periostin in the
vascular response to Injury. Arter.
Throm. and Vas. Bio. 2005; 25:77-83.
Conley
BA, Koleva R, Smith JD, Kacer D, Zhang D, Bernabeu C, and Vary
CPH. Endoglin Controls Cell Migration and Composition of Focal
Adhesions. J.
Biol. Chem.
2004; 279:27440-27449.
Full
Publication List
|
|
Lab
Photo
|
Left
to Right:
Cal Vary, Maria Mancini, Diana Romero, Barbara Conley, and Scott
Morin
|
|