Targets, models and challenges in osteoarthritis research

被引:238
作者
Thysen, Sarah [1 ]
Luyten, Frank P. [2 ,3 ]
Lories, Rik J. U. [1 ,3 ]
机构
[1] Katholieke Univ Leuven, Skeletal Biol & Engn Res Ctr, Lab Tissue Homeostasis & Dis, B-3000 Leuven, Belgium
[2] Katholieke Univ Leuven, Skeletal Biol & Engn Res Ctr, B-3000 Leuven, Belgium
[3] Katholieke Univ Leuven, Univ Hosp Leuven, Div Rheumatol, B-3000 Leuven, Belgium
关键词
Osteoarthritis; Cartilage; Bone; Animal models; CRUCIATE LIGAMENT TRANSECTION; BONE MORPHOGENETIC PROTEIN-7; MESENCHYMAL STEM-CELLS; HUMAN ARTICULAR CHONDROCYTES; FIBROBLAST GROWTH FACTOR-18; GENOME-WIDE ASSOCIATION; HIGH-RESOLUTION MRI; SUBCHONDRAL BONE; HISTOLOGICAL ASSESSMENTS; STRONTIUM RANELATE;
D O I
10.1242/dmm.016881
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Osteoarthritis is a chronic degenerative disorder of the joint and represents one of the most common diseases worldwide. Its prevalence and severity are increasing owing to aging of the population, but treatment options remain largely limited to painkillers and anti-inflammatory drugs, which only provide symptomatic relief. In the late stages of the disease, surgical interventions are often necessary to partially restore joint function. Although the focus of osteoarthritis research has been originally on the articular cartilage, novel findings are now pointing to osteoarthritis as a disease of the whole joint, in which failure of different joint components can occur. In this Review, we summarize recent progress in the field, including data from novel 'omics' technologies and from a number of preclinical and clinical trials. We describe different in vitro and in vivo systems that can be used to study molecules, pathways and cells that are involved in osteoarthritis. We illustrate that a comprehensive and multisystem approach is necessary to understand the complexity and heterogeneity of the disease and to better guide the development of novel therapeutic strategies for osteoarthritis.
引用
收藏
页码:17 / 30
页数:14
相关论文
共 181 条
[1]
LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS .3. REVERSIBLE BEHAVIOR OF CHONDROCYTES IN PRIMARY CULTURES [J].
ABBOTT, J ;
HOLTZER, H .
JOURNAL OF CELL BIOLOGY, 1966, 28 (03) :473-&
[2]
Suppression of pain and joint destruction by inhibition of the proteasome system in experimental osteoarthritis [J].
Ahmed, Aisha Siddiqah ;
Li, Jian ;
Erlandsson-Harris, Helena ;
Stark, Andre ;
Bakalkin, Georgy ;
Ahmed, Mahmood .
PAIN, 2012, 153 (01) :18-26
[3]
Strontium ranelate effect in postmenopausal women with different clinical levels of osteoarthritis [J].
Alexandersen, P. ;
Karsdal, M. A. ;
Byrjalsen, I. ;
Christiansen, C. .
CLIMACTERIC, 2011, 14 (02) :236-243
[4]
The diverse functions of Dot1 and H3K79 methylation [J].
Anh Tram Nguyen ;
Zhang, Yi .
GENES & DEVELOPMENT, 2011, 25 (13) :1345-1358
[5]
[Anonymous], EUR CELL MAT
[6]
A CHONDROGENIC CELL-LINE DERIVED FROM A DIFFERENTIATING CULTURE OF AT805 TERATOCARCINOMA CELLS [J].
ATSUMI, T ;
MIWA, Y ;
KIMATA, K ;
IKAWA, Y .
CELL DIFFERENTIATION AND DEVELOPMENT, 1990, 30 (02) :109-116
[7]
The protective effect of OP-1 on articular cartilage in the development of osteoarthritis [J].
Badlani, N. ;
Inoue, A. ;
Healey, R. ;
Coutts, R. ;
Amiel, D. .
OSTEOARTHRITIS AND CARTILAGE, 2008, 16 (05) :600-606
[8]
Use of Bone Morphogenic Protein-7 as a Treatment for Osteoarthritis [J].
Badlani, Neil ;
Oshima, Yasushi ;
Healey, Rob ;
Coutts, Richard ;
Amiel, David .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2009, 467 (12) :3221-3229
[9]
Targeting DOT1L action and interactions in leukemia: the role of DOT1L in transformation and development [J].
Barry, Evan R. ;
Corry, Gareth N. ;
Rasmussen, Theodore P. .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2010, 14 (04) :405-418
[10]
Transcriptomics of Wild-Type Mice and Mice Lacking ADAMTS-5 Activity Identifies Genes Involved in Osteoarthritis Initiation and Cartilage Destruction [J].
Bateman, John F. ;
Rowley, Lynn ;
Belluoccio, Daniele ;
Chan, Ben ;
Bell, Katrina ;
Fosang, Amanda J. ;
Little, Christopher B. .
ARTHRITIS AND RHEUMATISM, 2013, 65 (06) :1547-1560