Wnt signaling and osteoarthritis

被引:135
作者
Luyten, Frank P. [1 ]
Tylzanowski, Przemko [1 ]
Lories, Rik J. [1 ]
机构
[1] Katholieke Univ Leuven, Lab Skeletal Dev & Joint Disorders, Div Rheumatol, Dept Musculoskeletal Sci, B-3000 Louvain, Belgium
关键词
Cartilage; Bone biology; Wnt signaling; Osteoarthritis; Skeletogenesis; POLYMORPHISMS;
D O I
10.1016/j.bone.2008.12.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Osteoarthritis is a common disease, clinically manifested by joint pain, swelling and progressive loss of function. The severity of disease manifestations can vary but most of the patients only need intermittent symptom relief without major interventions. However, there is a group of patients that shows fast progression of the disease process leading to disability and ultimately joint replacement. Apart from symptom relief, no treatments have been identified that arrest or reverse the disease process. Therefore, there has been increasing attention devoted to the understanding of the mechanisms that are driving the disease process. Among these mechanisms, the biology of the cartilage-subchondral bone unit has been highlighted as key in osteoarthritis, and pathways that involve both cartilage and bone formation and turnover have become prime targets for modulation, and thus therapeutic intervention. Studies in developmental, genetic and joint disease models indicate that Writ signaling is critically involved in these processes. Consequently, targeting Writ signaling in a selective and tissue specific manner is an exciting opportunity for the development of disease modifying drugs for osteoarthritis. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:522 / 527
页数:6
相关论文
共 73 条
[1]   Bone biomechanical properties in LRP5 mutant mice [J].
Akhter, MP ;
Wells, DJ ;
Short, SJ ;
Cullen, DM ;
Johnson, ML ;
Haynatzki, GR ;
Babij, P ;
Allen, KM ;
Yaworsky, PJ ;
Bex, F ;
Recker, RR .
BONE, 2004, 35 (01) :162-169
[2]   Interactions between Sox9 and β-catenin control chondrocyte differentiation [J].
Akiyama, H ;
Lyons, JP ;
Mori-Akiyama, Y ;
Yang, XH ;
Zhang, R ;
Zhang, ZP ;
Deng, JM ;
Taketo, MM ;
Nakamura, T ;
Behringer, RR ;
McCrea, PD ;
de Crombrugghe, B .
GENES & DEVELOPMENT, 2004, 18 (09) :1072-1087
[3]  
ARCHER CW, 2003, BIRTH DEFECTS RES C, V2, P144
[4]   Angiogenesis in osteoarthritis [J].
Ashraf, Sadaf ;
Walsh, David Andrew .
CURRENT OPINION IN RHEUMATOLOGY, 2008, 20 (05) :573-580
[5]   Minireview:: The genetics of low-density lipoprotein Receptor-related protein 5 in bone:: A story of extremes [J].
Balemans, Wendy ;
Van Hul, Wim .
ENDOCRINOLOGY, 2007, 148 (06) :2622-2629
[6]   Synovial tissue inflammation in early and late osteoarthritis [J].
Benito, MJ ;
Veale, DJ ;
Fitzgerald, O ;
van den Berg, WB ;
Bresnihan, B .
ANNALS OF THE RHEUMATIC DISEASES, 2005, 64 (09) :1263-1267
[7]   The Wnt antagonist secreted frizzled-related protein-1 is a negative regulator of trabecular bone formation in adult mice [J].
Bodine, PVN ;
Zhao, WG ;
Kharode, YP ;
Bex, FJ ;
Lambert, AJ ;
Goad, MB ;
Gaur, T ;
Stein, GS ;
Lian, JB ;
Komm, BS .
MOLECULAR ENDOCRINOLOGY, 2004, 18 (05) :1222-1237
[8]   New insights into osteoarthritis: early developmental features of an ageing-related disease [J].
Bos, Steffan Daniel ;
Slagboom, P. Eline ;
Meulenbelt, Ingrid .
CURRENT OPINION IN RHEUMATOLOGY, 2008, 20 (05) :553-559
[9]   High bone density due to a mutation in LDL-receptor-related protein 5 [J].
Boyden, LM ;
Mao, JH ;
Belsky, J ;
Mitzner, L ;
Farhi, A ;
Mitnick, MA ;
Wu, DQ ;
Insogna, K ;
Lifton, RP .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (20) :1513-1521
[10]  
Burr DB, 2005, J RHEUMATOL, V32, P1156