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Glycogen synthase kinase-3 inhibitor as a multi-targeting anti-rheumatoid drug.
Arioka, Masaki; Takahashi-Yanaga, Fumi.
Afiliación
  • Arioka M; Department of Clinical Pharmacology, Faculty of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.
  • Takahashi-Yanaga F; Department of Pharmacology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan. Electronic address: ftakahashi@med.uoeh-u.ac.jp.
Biochem Pharmacol ; 165: 207-213, 2019 07.
Article en En | MEDLINE | ID: mdl-30776323
Rheumatoid arthritis (RA) is a chronic inflammatory joint disease that causes swelling, bone erosion, and joint disorder. Patients with RA therefore suffer from pain and physiological disability, and have a decreased quality of life. During the progression of RA, many different types of cells and inflammatory factors influence each other with an important role. A better understanding of the pathology of RA should therefore lead to the development of effective anti-rheumatoid drugs, such as the anti-TNFα antibody. Glycogen synthase kinase-3 (GSK-3) is a cytoplasmic serine/threonine protein kinase that is involved in a large number of key cellular processes and is dysregulated in a wide variety of diseases, including inflammation and osteoporosis. The accumulated evidence has suggested that GSK-3 could be involved in multiple steps in the progression of RA. In the present review, the mechanisms of the pathogenesis of RA are summarized, and recent developments and potential new drugs targeting GSK-3 are discussed.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antirreumáticos / Glucógeno Sintasa Quinasa 3 Tipo de estudio: Etiology_studies Aspecto: Patient_preference Límite: Animals / Humans Idioma: En Revista: Biochem Pharmacol Año: 2019 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Antirreumáticos / Glucógeno Sintasa Quinasa 3 Tipo de estudio: Etiology_studies Aspecto: Patient_preference Límite: Animals / Humans Idioma: En Revista: Biochem Pharmacol Año: 2019 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Reino Unido