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dc.contributor.author | Ferrandiz Manglano, Mª Luisa | es_ES |
dc.contributor.author | Nacher-Juan, Josep | es_ES |
dc.contributor.author | Alcaraz Tormo, Mª Jose | es_ES |
dc.date.accessioned | 2020-04-29T07:04:33Z | |
dc.date.available | 2020-04-29T07:04:33Z | |
dc.date.issued | 2018-06 | es_ES |
dc.identifier.issn | 0006-2952 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/141951 | |
dc.description.abstract | [EN] Nuclear factor (erythroid-derived 2)-like 2 (Nrf2) is a master regulator of cellular protective processes. Rheumatic diseases are chronic conditions characterized by inflammation, pain, tissue damage and limitations in function. Main examples are rheumatoid arthritis, systemic lupus erythematosus, osteoarthritis and osteoporosis. Their high prevalence constitutes a major health problem with an important social and economic impact. A wide range of evidence indicates that Nrf2 may control different mechanisms involved in the physiopathology of rheumatic conditions. Therefore, the appropriate expression and balance of Nrf2 is necessary for regulation of oxidative stress, inflammation, immune responses, and cartilage and bone metabolism. Numerous studies have demonstrated that Nrf2 deficiency aggravates the disease in experimental models while Nrf2 activation results in immunoregulatory and anti-inflammatory effects. These reports reinforce the increasing interest in the pharmacologic regulation of Nrf2 and its potential applications. Nevertheless, a majority of Nrf2 inducers are electrophilic molecules which may present off-target effects. In recent years, novel strategies have been sought to modulate the Nrf2 pathway which has emerged as a therapeutic target in rheumatic conditions. | es_ES |
dc.description.sponsorship | This work has been funded by grant SAF2017-85806-R (MINECO, FEDER, Spain). | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | Elsevier | es_ES |
dc.relation.ispartof | Biochemical Pharmacology | es_ES |
dc.rights | Reconocimiento - No comercial - Sin obra derivada (by-nc-nd) | es_ES |
dc.subject | Nrf2,Rheumatic conditions | es_ES |
dc.subject | Rheumatoid arthritis | es_ES |
dc.subject | Systemic lupus erythematosus | es_ES |
dc.subject | Osteoarthritis | es_ES |
dc.subject | Osteoporosis | es_ES |
dc.title | Nrf2 as a therapeutic target for rheumatic diseases | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1016/j.bcp.2018.04.010 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/SAF2017-85806-R/ES/MECANISMOS REGULADORES DE LA INFLAMACION Y SU RESOLUCION EN ENFERMEDADES CRONICAS ARTICULARES Y DE LA PIEL/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.description.bibliographicCitation | Ferrandiz Manglano, ML.; Nacher-Juan, J.; Alcaraz Tormo, MJ. (2018). Nrf2 as a therapeutic target for rheumatic diseases. Biochemical Pharmacology. 152:338-346. https://doi.org/10.1016/j.bcp.2018.04.010 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | http://doi.org/10.1016/j.bcp.2018.04.010 | es_ES |
dc.description.upvformatpinicio | 338 | es_ES |
dc.description.upvformatpfin | 346 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 152 | es_ES |
dc.identifier.pmid | 29660314 | es_ES |
dc.relation.pasarela | S\378194 | es_ES |
dc.contributor.funder | Ministerio de Economía y Competitividad | es_ES |
dc.contributor.funder | Agencia Estatal de Investigación | es_ES |