Epigenetics as a Therapeutic Target in Osteoarthritis

被引:10
|
作者
Nunez-Carro, Carmen [1 ]
Blanco-Blanco, Margarita [1 ]
Mariuxi Villagran-Andrade, Karla [1 ]
Blanco, Francisco J. [1 ,2 ]
de Andres, Maria C. [1 ]
机构
[1] Complexo Hosp Univ, Grp Invest Reumatol GIR, Inst Invest Biomed A Coruna INIBIC, Unidad Epigenet,A Coruna CHUAC, La Coruna 15006, Spain
[2] Univ Coruna UDC, Fac Fisioterapia, Dept Fisioterapia Med & Ciencias Biomed, Grp Invest Reumatol & Salud, Campus Oza, La Coruna 15008, Spain
关键词
epigenetics; osteoarthritis; DNA methylation; histone methylation; histone acetylation; miRNA; circRNA; lncRNA; HUMAN ARTICULAR CHONDROCYTES; DNA METHYLATION; CHONDROGENIC DIFFERENTIATION; INFLAMMATORY RESPONSE; HISTONE DEACETYLASE-4; MICRORNA EXPRESSION; OXIDATIVE STRESS; GENE-EXPRESSION; SYNOVIAL-FLUID; CPG SITES;
D O I
10.3390/ph16020156
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Osteoarthritis (OA) is a heterogenous, complex disease affecting the integrity of diarthrodial joints that, despite its high prevalence worldwide, lacks effective treatment. In recent years it has been discovered that epigenetics may play an important role in OA. Our objective is to review the current knowledge of the three classical epigenetic mechanisms-DNA methylation, histone post-translational modifications (PTMs), and non-coding RNA (ncRNA) modifications, including microRNAs (miRNAs), circular RNAs (circRNAs), and long non-coding RNAs (lncRNAs)-in relation to the pathogenesis of OA and focusing on articular cartilage. The search for updated literature was carried out in the PubMed database. Evidence shows that dysregulation of numerous essential cartilage molecules is caused by aberrant epigenetic regulatory mechanisms, and it contributes to the development and progression of OA. This offers the opportunity to consider new candidates as therapeutic targets with the potential to attenuate OA or to be used as novel biomarkers of the disease.
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页数:27
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