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Oxidative Stress Modulation by ncRNAs and Their Emerging Role as Therapeutic Targets in Atherosclerosis and Non-Alcoholic Fatty Liver Disease

dc.contributor.authorInfante-Menéndez, Jorge
dc.contributor.authorGonzález-López, Paula
dc.contributor.authorHuertas-Lárez, Raquel
dc.contributor.authorGómez Hernández, María De La Almudena
dc.contributor.authorEscribano Illanes, Óscar
dc.date.accessioned2024-06-24T11:54:06Z
dc.date.available2024-06-24T11:54:06Z
dc.date.issued2023-01-24
dc.description.abstractAtherosclerosis and non-alcoholic fatty liver disease (NAFLD) are pathologies related to ectopic fat accumulation, both of which are continuously increasing in prevalence. These threats are prompting researchers to develop effective therapies for their clinical management. One of the common pathophysiological alterations that underlies both diseases is oxidative stress (OxS), which appears as a result of lipid deposition in affected tissues. However, the molecular mechanisms that lead to OxS generation are different in each disease. Non-coding RNAs (ncRNAs) are RNA transcripts that do not encode proteins and function by regulating gene expression. In recent years, the involvement of ncRNAs in OxS modulation has become more recognized. This review summarizes the most recent advances regarding ncRNA-mediated regulation of OxS in atherosclerosis and NAFLD. In both diseases, ncRNAs can exert pro-oxidant or antioxidant functions by regulating gene targets and even other ncRNAs, positioning them as potential therapeutic targets. Interestingly, both diseases have common altered ncRNAs, suggesting that the same molecule can be targeted simultaneously when both diseases coexist. Finally, since some ncRNAs have already been used as therapeutic agents, their roles as potential drugs for the clinical management of atherosclerosis and NAFLD are analyzed.
dc.description.departmentDepto. de Bioquímica y Biología Molecular
dc.description.facultyFac. de Farmacia
dc.description.fundingtypeDescuento UCM
dc.description.refereedTRUE
dc.description.sponsorshipMinisterio de Ciencia e Innovación (España)
dc.description.statuspub
dc.identifier.citationInfante-Menéndez, J.; González-López, P.; Huertas-Lárez, R.; Gómez-Hernández, A.; Escribano, Ó. Oxidative Stress Modulation by ncRNAs and Their Emerging Role as Therapeutic Targets in Atherosclerosis and Non-Alcoholic Fatty Liver Disease. Antioxidants 2023, 12, 262. https://doi.org/10.3390/antiox12020262
dc.identifier.doi10.3390/antiox12020262
dc.identifier.issn2076-3921
dc.identifier.officialurlhttps://doi.org/10.3390/antiox12020262
dc.identifier.relatedurlhttps://www.mdpi.com/2076-3921/12/2/262
dc.identifier.urihttps://hdl.handle.net/20.500.14352/105196
dc.issue.number2
dc.journal.titleAntioxidants
dc.language.isoeng
dc.page.initial262
dc.publisherMDPI
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica de Innovación 2021-2023/PID2021-123076OB-I00/MODULACIÓN DE MIR-155-5P, MIR-149-5P, LET-7D-5P Y MIR-143-3P COMO APROXIMACIÓN TERAPÉUTICA PARA LA ENFERMEDAD DEL HÍGADO GRASO NO ALCOHÓLICO Y LA ATEROSCLEROSIS
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu577.1
dc.subject.cdu612.015
dc.subject.keywordOxidative stress
dc.subject.keywordatherosclerosis
dc.subject.keywordNAFLD
dc.subject.keywordncRNAs
dc.subject.keywordmiRNAs
dc.subject.keywordlncRNAs
dc.subject.keywordcircRNAs
dc.subject.keywordRNA-based therapies
dc.subject.ucmCiencias Biomédicas
dc.subject.ucmBiología molecular (Farmacia)
dc.subject.ucmBioquímica (Farmacia)
dc.subject.unesco32 Ciencias Médicas
dc.titleOxidative Stress Modulation by ncRNAs and Their Emerging Role as Therapeutic Targets in Atherosclerosis and Non-Alcoholic Fatty Liver Disease
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number12
dspace.entity.typePublication
relation.isAuthorOfPublication57e2f68c-6c43-42db-88b2-b5ee5add57a7
relation.isAuthorOfPublicationda39ae63-c1a5-4c1e-8ade-a0b92136cd41
relation.isAuthorOfPublication.latestForDiscovery57e2f68c-6c43-42db-88b2-b5ee5add57a7

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