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dc.contributor.authorAlique Aguilar, Matilde 
dc.contributor.authorSánchez-López E, Elsa
dc.contributor.authorBodega Magro, Guillermo 
dc.contributor.authorGiannarelli, Chiara
dc.contributor.authorCarracedo Añón, Julia María 
dc.contributor.authorRamírez Chamond, Manuel Rafael 
dc.date.accessioned2022-03-28T07:30:24Z
dc.date.available2022-03-28T07:30:24Z
dc.date.issued2020-01-20
dc.identifier.bibliographicCitationAlique M, Sánchez-López E, Bodega G, Giannarelli C, Carracedo J, Ramírez R. Hypoxia-Inducible Factor-1α: The Master Regulator of Endothelial Cell Senescence in Vascular Aging. Cells. 2020; 9(1):195en
dc.identifier.issn2073-4409
dc.identifier.urihttp://hdl.handle.net/10017/51267
dc.description.abstractAging is one of the hottest topics in biomedical research. Advances in research and medicine have helped to preserve human health, leading to an extension of life expectancy. However, the extension of life is an irreversible process that is accompanied by the development of aging-related conditions such as weakness, slower metabolism, and sti ness of vessels. It also debated that aging can be considered an actual disease with aging-derived comorbidities, including cancer or cardiovascular disease. Currently, cardiovascular disorders, including atherosclerosis, are considered as premature aging and represent the first causes of death in developed countries, accounting for 31% of annual deaths globally. Emerging evidence has identified hypoxia-inducible factor-1 as a critical transcription factor with an essential role in aging-related pathology, in particular, regulating cellular senescence associated with cardiovascular aging. In this review, we will focus on the regulation of senescence mediated by hypoxia-inducible factor-1 in age-related pathologies, with particular emphasis on the crosstalk between endothelial and vascular cells in age-associated atherosclerotic lesions. More specifically, we will focus on the characteristics and mechanisms by which cells within the vascular wall, including endothelial and vascular cells, achieve a senescent phenotype.en
dc.description.sponsorshipInstituto de Salud Carlos IIIes
dc.description.sponsorshipSociedad Española de Nefrologíaes
dc.description.sponsorshipUniversidad de Alcaláes
dc.description.sponsorshipGrupo Santanderes
dc.description.sponsorshipUniversity of California San Diegoen
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.rights© 2020 by the authors. Licensee MDPI, Basel, Switzerlanden
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.subjectHypoxia-inducible factor-1alfa (HIF1alfa)en
dc.subjectVascular agingen
dc.subjectSenescent cellsen
dc.subjectEndothelial cellsen
dc.subjectVascular smooth muscle cellsen
dc.subjectAtherosclerosisen
dc.subjectExtracellular vesiclesen
dc.titleHypoxia-Inducible Factor-1alfa: The Master Regulator of Endothelial Cell Senescence in Vascular Agingen
dc.typeinfo:eu-repo/semantics/articleen
dc.subject.ecienciaMedicinaes
dc.subject.ecienciaMedicineen
dc.contributor.affiliationUniversidad de Alcalá. Departamento Biomedicina y Biotecnologíaes
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Biología de Sistemases
dc.date.updated2022-03-28T07:26:42Z
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.3390/cells9010195
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII/PI19%2F00240/ES/Proyectos de Investigación en Saluden
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII/PI17%2F01029/ES/Proyectos de Investigación en Saluden
dc.relation.projectIDinfo:eu-repo/grantAgreement/Grupo Santander%2FUCM/PR41%2F17-20964en
dc.relation.projectIDinfo:eu-repo/grantAgreement/UAH//GP-2018-4en
dc.relation.projectIDinfo:eu-repo/grantAgreement/UAH//CGC2018%2FBIO-012en
dc.relation.projectIDinfo:eu-repo/grantAgreement/UCSD//P30AR073761en
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen
dc.identifier.uxxiAR/0000032975
dc.identifier.publicationtitleCellsen
dc.identifier.publicationvolume9
dc.identifier.publicationissue1
dc.identifier.publicationfirstpage195


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© 2020 by the authors. Licensee MDPI, Basel, Switzerland
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