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Inside human aortic stenosis: a proteomic analysis of plasma

dc.contributor.authorGil Dones, Félix
dc.contributor.authorDarde, Verónica
dc.contributor.authorAlonso-Orgaz, Sergio
dc.contributor.authorLopez-Almodovar, Luis
dc.contributor.authorMourino-Alvarez, Laura
dc.contributor.authorPadial, Luis
dc.contributor.authorVivanco, Fernando
dc.contributor.authorBarderas, Maria
dc.date.accessioned2024-01-23T08:57:50Z
dc.date.available2024-01-23T08:57:50Z
dc.date.issued2012
dc.descriptionThis work was supported by grants from the Instituto de Salud Carlos III (FIS PI070537, CP09/00229), Fondo de Investigación Sanitaria de Castilla la Mancha (FISCAM, PI2008/28 and PI2008/08) and Redes Temáticas de Investigación Cooperativa (FONDOS FEDER, RD06/0014/1015), CNIC.
dc.description.abstractValvular aortic stenosis (AS) produces a slowly progressive obstruction in left ventricular outflow track. For this reason, aortic valve replacement is warranted when the valvular stenosis is hemodinamically significant, becoming the most common worldwide cause of aortic valve surgery. Recent epidemiologic studies have revealed an association between degenerative AS and cardiovascular risk factors for atherosclerosis, althought reducing the exposure to such factors and statin therapies both fail to delay or reverse the pathology. Hence, a deeper understanding of the pathophysiology of this disease is required to identify appropriate preventive measures. A proteomic analysis of plasma will permit to know and identify the changes in protein expression induced by AS in this tissue. Using two-dimensional difference gel electrophoresis (2D-DIGE) followed by mass spectrometry (MS), we compared the crude (not pre-fractioned) and pre-fractioned plasma from AS patients and control subjects. We sought to identify plasma proteins whose expression is modified in AS. In addition we investigated if crude plasma presented some alterations in the more abundant proteins since to date, has never been studied before. We also further investigated the link between this disease and atherosclerosis with a view to identifying new potential markers and therapeutic targets.
dc.description.departmentDepto. de Genética, Fisiología y Microbiología
dc.description.facultyFac. de Ciencias Biológicas
dc.description.refereedTRUE
dc.description.sponsorshipInstituto de Salud Carlos III
dc.description.sponsorshipJunta de Comunidades de Castilla-La Mancha
dc.description.sponsorshipEuropean Commission
dc.description.statuspub
dc.identifier.citationGil-Dones, Félix, et al. «Inside Human Aortic Stenosis: A Proteomic Analysis of Plasma». Journal of Proteomics, vol. 75, n.o 5, febrero de 2012, pp. 1639-53. https://doi.org/10.1016/j.jprot.2011.11.036.
dc.identifier.doi10.1016/j.jprot.2011.11.036
dc.identifier.issn1874-3919
dc.identifier.officialurlhttps://doi.org/10.1016/j.jprot.2011.11.036
dc.identifier.urihttps://hdl.handle.net/20.500.14352/94604
dc.issue.number5
dc.journal.titleJournal of Proteomics
dc.language.isoeng
dc.page.final1653
dc.page.initial1639
dc.publisherElsevier
dc.rights.accessRightsrestricted access
dc.subject.cdu577.112
dc.subject.cdu577.21
dc.subject.cdu616.12
dc.subject.keywordAortic stenosis
dc.subject.keywordDiseases proteomics
dc.subject.keywordBiomarkers
dc.subject.keywordTwo dimensional fluorescence difference gel electrophoresis (2D-DIGE)
dc.subject.keywordCombinatorial peptide ligand library (CPLL)
dc.subject.keywordImmunoaffinity depletion of high-abundance proteins
dc.subject.ucmBioquímica (Biología)
dc.subject.ucmGenética
dc.subject.ucmCardiología
dc.subject.unesco2403 Bioquímica
dc.subject.unesco2409 Genética
dc.subject.unesco3205.01 Cardiología
dc.titleInside human aortic stenosis: a proteomic analysis of plasma
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number75
dspace.entity.typePublication
relation.isAuthorOfPublication0827e638-921a-4475-9a48-b859587719c5
relation.isAuthorOfPublication.latestForDiscovery0827e638-921a-4475-9a48-b859587719c5

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