scholarly journals Regulation of fibronectin and metalloproteinase expression by Wnt signaling in rheumatoid arthritis synoviocytes

2002 ◽  
Vol 46 (11) ◽  
pp. 2867-2877 ◽  
Author(s):  
Malini Sen ◽  
Jack Reifert ◽  
Kevin Lauterbach ◽  
Vladimir Wolf ◽  
Jeffrey S. Rubin ◽  
...  
2019 ◽  
Vol 20 (22) ◽  
pp. 5525 ◽  
Author(s):  
Kazuhiro Maeda ◽  
Yasuhiro Kobayashi ◽  
Masanori Koide ◽  
Shunsuke Uehara ◽  
Masanori Okamoto ◽  
...  

Wnt, a secreted glycoprotein, has an approximate molecular weight of 40 kDa, and it is a cytokine involved in various biological phenomena including ontogeny, morphogenesis, carcinogenesis, and maintenance of stem cells. The Wnt signaling pathway can be classified into two main pathways: canonical and non-canonical. Of these, the canonical Wnt signaling pathway promotes osteogenesis. Sclerostin produced by osteocytes is an inhibitor of this pathway, thereby inhibiting osteogenesis. Recently, osteoporosis treatment using an anti-sclerostin therapy has been introduced. In this review, the basics of Wnt signaling, its role in bone metabolism and its involvement in skeletal disorders have been covered. Furthermore, the clinical significance and future scopes of Wnt signaling in osteoporosis, osteoarthritis, rheumatoid arthritis and neoplasia are discussed.


2014 ◽  
Vol 50 ◽  
pp. 59-66 ◽  
Author(s):  
Sinisa Savic ◽  
Lylia Ouboussad ◽  
Laura J. Dickie ◽  
Janina Geiler ◽  
Chi Wong ◽  
...  

2014 ◽  
Vol 73 (Suppl 1) ◽  
pp. A8.1-A8
Author(s):  
Paola Bonaventura ◽  
Fabien Lavocat ◽  
Giulia Benedetti ◽  
Aline Lambroux ◽  
Francis Albarede ◽  
...  

Fitoterapia ◽  
2019 ◽  
Vol 139 ◽  
pp. 104402 ◽  
Author(s):  
Anna Jesionek ◽  
Adam Kokotkiewicz ◽  
Anna Mikosik-Roczynska ◽  
Klaudia Ciesielska-Figlon ◽  
Piotr Luczkiewicz ◽  
...  

2015 ◽  
Vol 2015 ◽  
pp. 1-10 ◽  
Author(s):  
Geng Yin ◽  
Ying Wang ◽  
Xiao-min Cen ◽  
Min Yang ◽  
Yan Liang ◽  
...  

Rheumatoid arthritis (RA) is a systemic autoimmune disease characterized by chronic inflammation of multiple joints. The central pathogenesis of RA is the proliferation of synovial fibroblasts in response to inflammatory cytokines. However, some of the targeted therapies for inflammation reactions do not display significant clinical improvement after initiation of therapy. Thus, the relationship between inflammatory responses and RA therapy is still incompletely understood. In the present study, we proposed to determine whether enhanced inflammations may lead to cell apoptosis in rheumatoid arthritis synoviocytes. Our results indicated that products of lipid peroxidations, 4-HNE, may induce synovial intrinsic inflammations by activating NF-κB pathways and it may lead to cell apoptosis. Pharmacological inhibition of NF-κB activation may reduce the 4-HNE mediated inflammation responses and subsequent cell apoptosis. Our results may help to clarify the role of inflammations on RA development and imply that blocking NF-κB activation may be partly beneficial for human RA therapy. These findings might provide a mechanism-based rationale for developing new strategy to RA clinical therapy.


2013 ◽  
Vol 25 (10) ◽  
pp. 2069-2078 ◽  
Author(s):  
Cheng-gui Miao ◽  
Ying-ying Yang ◽  
Xu He ◽  
Xiao-feng Li ◽  
Cheng Huang ◽  
...  

1996 ◽  
Vol 39 (1) ◽  
pp. 125-136 ◽  
Author(s):  
Carlene Tsai ◽  
Luis A. Diaz ◽  
Nora G. Singer ◽  
Lan Lan Li ◽  
Anita H. Kirsch ◽  
...  

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