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dc.contributor.authorAlique Aguilar, Matilde 
dc.contributor.authorCeprían, Noemí
dc.contributor.authorRamírez Chamond, Manuel Rafael 
dc.contributor.authorFiguer Rubio, Andrea 
dc.contributor.authorValera, Gemma
dc.contributor.authorBodega Magro, Guillermo 
dc.date.accessioned2022-03-28T07:47:09Z
dc.date.available2022-03-28T07:47:09Z
dc.date.issued2022-02-04
dc.identifier.bibliographicCitationJournal of Personalized Medicine, 2022, v. 12, n. 215en
dc.identifier.issn2075-4426
dc.identifier.urihttp://hdl.handle.net/10017/51249en
dc.description.abstractAtherosclerosis is probably one of the paradigms of disease linked to aging. Underlying the physiopathology of atherosclerosis are cellular senescence, oxidative stress, and inflammation. These factors are increased in the elderly and from chronic disease patients. Elevated levels of oxidative stress affect cellular function and metabolism, inducing senescence. This senescence modifies the cell phenotype into a senescent secretory phenotype. This phenotype activates immune cells, leading to chronic systemic inflammation. Moreover, due to their secretory phenotype, senescence cells present an increased release of highlighted extracellular vesicles that will change nearby/neighborhood cells and paracrine signaling. For this reason, searching for specific senescent cell biomarkers and therapies against the development/killing of senescent cells has become relevant. Recently, senomorphic and senolityc drugs have become relevant in slowing down or eliminating senescence cells. However, even though they have shown promising results in experimental studies, their clinical use is still yet to be determineden
dc.description.sponsorshipInstituto de Salud Carlos IIIes
dc.description.sponsorshipSociedad Española de Nefrologíaes
dc.description.sponsorshipComunidad de Madrides
dc.description.sponsorshipFondo Europeo de Desarrollo Regionales
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
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.subjectAtherosclerosisen
dc.subjectCellular senescenceen
dc.subjectEndothelial senescenceen
dc.subjectExtracellular vesiclesen
dc.subjectInflammationen
dc.subjectSenolitycen
dc.titleEndothelial Senescence and the Chronic Vascular Diseases: Challenges and Therapeutic Opportunities in Atherosclerosisen
dc.typeinfo:eu-repo/semantics/articleen
dc.subject.ecienciaFisiologíaes_ES
dc.subject.ecienciaPhysiologyen
dc.contributor.affiliationUniversidad de Alcalá. Departamento de Biología de Sistemases_ES
dc.date.updated2022-03-28T07:46:40Z
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.3390/jpm12020215
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII//PI19%2F00240es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII//PI17%2F01029en
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII//PI20%2F01321en
dc.relation.projectIDinfo:eu-repo/grantAgreement/ISCIII//PI20%2F00018en
dc.relation.projectIDinfo:eu-repo/grantAgreement/CM-FEDER// PEJ-2020-AI%2FBMD-18141en
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen
dc.identifier.uxxiAR/0000040982en
dc.identifier.publicationtitleJournal of Personalized Medicineen
dc.identifier.publicationvolume12
dc.identifier.publicationissue215


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