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Josep Maria de Anta Vinyals
Associate Professor of Embriology and Human Anatomy
Professor Agregat d'Anatomia i Embriologia Humana
E-mail: janta@ub.edu
Phone: +3493 4021904
Research Interests
and Current Projects
Our main research
interest is focused the genetic basis of arteriogenesis in the heart
(coronary collateral circulation). We are searching molecular determinants
of collateral circulation in coronary artery disease patients. In particular,
we are studying the role of functional SNP genotypes in arteriogenic
and angiogenic genes, as well as the functional responses of endothelial
progenitor cells from coronary artery patients to fluid shear stress
in relation with collateral circulation. Other approach is based on
an experimental model of arteriogenesis to evaluate the effect of hypercholesterolemia
on Notch signaling pathway during arteriogenesis.
Our group is also
interested in the genetic basis of human anatomical variations, in particular
on coronary artery patterning and its importance in myocardial perfusion.
This investigation has been supported by several grants from University
of Barcelona (ACESBELL).
Our
group
Our group includes
several members with a large experience in cellular and molecular biology,
anatomical dissection and also in morphology techniques:
- Josep Maria
de Anta. Ph.D. Associate Professor of Human Anatomy and Embryology.
- Víctor J. Götzens. Ph.D. Associate Professor of Human Anatomy and Embryology.
- Joan Duran, Ph.D. Assistant
Professsor of Human Anatomy and Embryology.
- Alex Cordero, B.Sc.
PhD fellow.
Our team also
includes cardiologists from two reference hospitals
of Barcelona (Centre Cardiovascular
Sant Jordi and Hospital Universitari
Vall d’Hebron)
Current projects
- Genetic susceptibility
to coronary neovascularisation in patients with coronary heart disease:
an approach based on single nucleotide polymorphism genotyping of genes
involved in arteriogenesis and angiogenesis. Fundació La Marató de
TV3 (Ref. 20080810). 2009-12. IP.
- Effect of hypercholesterolemia
in Notch signalling pathway during arteriogenesis in mice with hindlimb
ischemia. ACESBELL 09. University of Barcelona. 2009-10
- Fluid shear stress
responses in endothelial progenitor cells from coronary artery patients
as determinants of coronary collateral circulation. IP. Fondo de Investigación
Sanitaria. Spanish Ministery of Health. Submitted 2010. IP
- Effect of hypercholesterolemia
in Notch signalling pathway during arteriogenesis in mice with hindlimb
ischemia and its reversion by simvastatina. Importance in coronary collateral
circulation. Grants on Basic Cardiology. Spanish Society of Cardiology.
Submitted 2010.
Selected Recent
Publications and Congress
Former research has been focused
on the study of mechanisms of resistance to antimetabolites in colon
adenocarcinoma cell lines, activities supported by several competitive
grants that have resulted in several publications:
- De Anta, J.M., Real,
F.X., Mayol, X. Low tumor cell density environment yields survival advantage
of tumor cells exposed to MTX in vitro. Biochim Biophys Acta. 2005 Jan
18;1721(1-3):98-106. Epub 2004 Nov 4.
- De Anta, J.M., Real,
F.X., Mayol, X. Methotrexate resistance in vitro is achieved by a dynamic
selection process of tumor cell variants emerging during treatment.
Int J Cancer. 2006 Oct 1;119(7):1607-15.
- De Anta, J.M., Pérez-Castro,
A.J., Real, F.X., Freire, R. and Mayol, X. The DNA damage checkpoint
is activated during residual tumour cell survival to methotrexate treatment
as an initial step of acquired drug resistance. Anticancer Drugs. 2006
Nov;17(10):1171-1177.
Congress and publications
regarding current research:
- De Anta, JM, Ramírez,
M, Buxeda, M, Sánchez, E, Götzens, V, Duran, J, Ortiz, JC.
VEGFA and KDR single nucleotide polymorphisms and coronary
artery variations in hearts from human cadaver specimens. 104th International
Meeting of the Anatomische Gesellschaft. Antwerpen. Belgium. 2009.
- Duran J, Götzens V,
Cordero A, Carballo, J, Petit M, de Anta JM. Coronary arterial branching
is associated with +405 VEGFA genotypes. Clinical implications
for myocardial infarction. In preparation. 2010.
- Cordero A, Carballo,
J, Duran J, Götzens V, Petit M, de Anta JM. +469G ICAM1 allele is associated
with low collateral support in coronary artery disease patients. En
preparación.
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