dc.contributor.author |
Alcaraz Tormo, Mª José
|
es_ES |
dc.contributor.author |
Guillen Salazar, Mª Isabel
|
es_ES |
dc.contributor.author |
Ferrándiz Manglano, Mª Luisa
|
es_ES |
dc.date.accessioned |
2020-06-02T05:37:35Z |
|
dc.date.available |
2020-06-02T05:37:35Z |
|
dc.date.issued |
2019-07 |
es_ES |
dc.identifier.issn |
0006-2952 |
es_ES |
dc.identifier.uri |
http://hdl.handle.net/10251/144825 |
|
dc.description.abstract |
[EN] Osteoarthritis (OA) is the most common joint disorder and a leading cause of disability. Current treatments for OA can improve symptoms but do not delay the progression of disease. In the last years, much effort has been devoted to developing new treatments for OA focused on pain control, inflammatory mediators or degradation of articular tissues. Although promising results have been obtained in ex vivo studies and animal models of OA, few of these agents have completed clinical trials. Available clinical data support the interest of nerve growth factor as a target in pain control as well as the disease-modifying potential of inhibitors of Wnt signaling or catabolic enzymes such as aggrecanases and cathepsin K, and anabolic strategies like fibroblast growth factor-18 or cellular therapies. Carefully controlled studies in patients selected according to OA phenotypes and with a long follow-up will help to confirm the relevance of these new approaches as emerging therapeutic treatments in OA. |
es_ES |
dc.description.sponsorship |
This work has been funded by grant SAF2017-85806-R (Ministerio de Ciencia, Educacion y Universidades, Spain, FEDER). |
es_ES |
dc.language |
Inglés |
es_ES |
dc.publisher |
Elsevier |
es_ES |
dc.relation.ispartof |
Biochemical Pharmacology |
es_ES |
dc.rights |
Reserva de todos los derechos |
es_ES |
dc.subject |
Osteoarthritis |
es_ES |
dc.subject |
Pain |
es_ES |
dc.subject |
Inflammatory mediators |
es_ES |
dc.subject |
Structural alterations |
es_ES |
dc.subject |
Nerve growth factor |
es_ES |
dc.subject |
Wnt |
es_ES |
dc.subject |
ADAMTS |
es_ES |
dc.subject |
Cathepsin K |
es_ES |
dc.subject |
Fibroblast growth factor-18 |
es_ES |
dc.subject |
Cellular therapy |
es_ES |
dc.title |
Emerging therapeutic agents in osteoarthritis |
es_ES |
dc.type |
Artículo |
es_ES |
dc.identifier.doi |
10.1016/j.bcp.2019.02.034 |
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 |
Cerrado |
es_ES |
dc.description.bibliographicCitation |
Alcaraz Tormo, MJ.; Guillen Salazar, MI.; Ferrándiz Manglano, ML. (2019). Emerging therapeutic agents in osteoarthritis. Biochemical Pharmacology. 165:4-16. https://doi.org/10.1016/j.bcp.2019.02.034 |
es_ES |
dc.description.accrualMethod |
S |
es_ES |
dc.relation.publisherversion |
https://doi.org/10.1016/j.bcp.2019.02.034 |
es_ES |
dc.description.upvformatpinicio |
4 |
es_ES |
dc.description.upvformatpfin |
16 |
es_ES |
dc.type.version |
info:eu-repo/semantics/publishedVersion |
es_ES |
dc.description.volume |
165 |
es_ES |
dc.relation.pasarela |
S\403088 |
es_ES |
dc.contributor.funder |
Agencia Estatal de Investigación |
|