Publication:
Telomerase as a Therapeutic Target in Cardiovascular Disease.

dc.contributor.authorHoffmann, Jedrzej
dc.contributor.authorRichardson, Gavin
dc.contributor.authorHaendeler, Judith
dc.contributor.authorAltschmied, Joachim
dc.contributor.authorAndres, Vicente
dc.contributor.authorSpyridopoulos, Ioakim
dc.contributor.funderMinisterio de Ciencia e Innovación (España)es_ES
dc.contributor.funderInstituto de Salud Carlos IIIes_ES
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)es_ES
dc.contributor.funderProgeria Research Foundationes_ES
dc.contributor.funderBritish Heart Foundationes_ES
dc.contributor.funderNational Institute for Health Research (Reino Unido)es_ES
dc.contributor.funderNewcastle Biomedical Research Centrees_ES
dc.contributor.funderTyne Hospitals NHS Foundation Trustes_ES
dc.contributor.funderDeutsche Forschungsgemeinschaft (Alemania)es_ES
dc.contributor.funderTelomerase Activator to Reverse Immunosenescence in Acute Coronary Syndromees_ES
dc.date.accessioned2022-11-21T11:38:09Z
dc.date.available2022-11-21T11:38:09Z
dc.date.issued2021
dc.description.abstractShortened telomeres have been linked to numerous chronic diseases, most importantly coronary artery disease, but the underlying mechanisms remain ill defined. Loss-of-function mutations and deletions in telomerase both accelerate telomere shortening but do not necessarily lead to a clinical phenotype associated with atherosclerosis, questioning the causal role of telomere length in cardiac pathology. The differential extranuclear functions of the 2 main components of telomerase, telomerase reverse transcriptase and telomerase RNA component, offer important clues about the complex relationship between telomere length and cardiovascular pathology. In this review, we critically discuss relevant preclinical models, genetic disorders, and clinical studies to elucidate the impact of telomerase in cardiovascular disease and its potential role as a therapeutic target. We suggest that the antioxidative function of mitochondrial telomerase reverse transcriptase might be atheroprotective, making it a potential target for clinical trials. Graphic Abstract: A graphic abstract is available for this article.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipWork in the VA laboratory is supported by the Spanish Ministerio de Ciencia e Innovación (MCIN) (PID2019-108489RB-I00) and the Instituto de Salud Carlos III (ISCIII) (AC17/00067) with co-funding from the European Regional Development Fund (ERDF, “Una manera de hacer Europa”), and the Progeria Research Foundation (Award PRF 2019–77). The CNIC is supported by the ISCIII, the MCIN, and the Pro CNIC Foundation. I. Spyridopoulos is funded by the British Heart Foundation (PG/18/25/33587) and National Institute for Health Research (NIHR) Newcastle Biomedical Research Centre based at Newcastle upon Tyne Hospitals NHS Foundation Trust and Newcastle University. The work of J. Haendeler and J. Altschmied is in part supported by the Deutsche Forschungsgemeinschaft (DFG) SFB1116, A04 (J. Haendeler and J. Altschmied), HA2868/14-1 (J. Haendeler) and AL288/5-1 (J. Altschmied). The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health’. I. Spyridopoulos also receives a grant from TA-Science for the TACTIC trial (Telomerase Activator to Reverse Immunosenescence in Acute Coronary Syndrome).es_ES
dc.format.number3es_ES
dc.format.page1047-1061es_ES
dc.format.volume41es_ES
dc.identifier.citationArterioscler Thromb Vasc Biol. 2021 Mar;41(3):1047-1061.es_ES
dc.identifier.doi10.1161/ATVBAHA.120.315695es_ES
dc.identifier.e-issn1524-4636es_ES
dc.identifier.journalArteriosclerosis, thrombosis, and vascular biologyes_ES
dc.identifier.pubmedID33504179es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/15207
dc.language.isoenges_ES
dc.publisherAmerican Heart Association (AHA)es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/PID2019-108489RB-I00es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/AC17/00067es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/PRF/2019–77es_ES
dc.relation.publisherversion10.1161/ATVBAHA.120.315695es_ES
dc.repisalud.institucionCNICes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Fisiopatología Cardiovascular Molecular y Genéticaes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshAnimalses_ES
dc.subject.meshBiomarkerses_ES
dc.subject.meshCardiovascular Diseaseses_ES
dc.subject.meshClinical Trials as Topices_ES
dc.subject.meshDrugs, Chinese Herbales_ES
dc.subject.meshExercisees_ES
dc.subject.meshGenome-Wide Association Studyes_ES
dc.subject.meshHumanses_ES
dc.subject.meshHydroxymethylglutaryl-CoA Reductase Inhibitorses_ES
dc.subject.meshLeukocyteses_ES
dc.subject.meshMicees_ES
dc.subject.meshModels, Cardiovasculares_ES
dc.subject.meshMutationes_ES
dc.subject.meshRNAes_ES
dc.subject.meshTelomerasees_ES
dc.subject.meshTelomere Homeostasises_ES
dc.subject.meshTelomere Shorteninges_ES
dc.titleTelomerase as a Therapeutic Target in Cardiovascular Disease.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication3bb85851-071a-490a-976b-c234983847a7
relation.isAuthorOfPublication.latestForDiscovery3bb85851-071a-490a-976b-c234983847a7

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