Vertical inhibition of the PI3K/Akt/mTOR pathway for the treatment of osteoarthritis

被引:137
作者
Chen, Jiezhong [1 ,2 ]
Crawford, Ross [1 ]
Xiao, Yin [1 ]
机构
[1] Queensland Univ Technol, Inst Hlth & Biomed Innovat, Brisbane, Qld 4059, Australia
[2] Univ Wollongong, Illawarra Hlth & Med Res Inst, Wollongong, NSW 2522, Australia
关键词
OSTEOARTHRITIS; EXTRACELLULAR MATRIX METALLOPROTEINASES; AUTOPHAGY; PI3K; Akt PATHWAY; ARTICULAR-CARTILAGE CHONDROCYTES; OBESITY-ASSOCIATED CANCER; B TRANSCRIPTION FACTORS; GENE-EXPRESSION; MAP KINASES; ACTIVATION; AUTOPHAGY; RAPAMYCIN; MMP-13; CELLS;
D O I
10.1002/jcb.24362
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Osteoarthritis is characterized by degenerative alterations of articular cartilage including both the degradation of extracellular matrix and the death of chondrocytes. The PI3K/Akt pathway has been demonstrated to involve in both processes. Inhibition of its downstream target NF-kB reduces the degradation of extracellular matrix via decreased production of matrix metalloproteinases while inhibition of mTOR increased autophagy to reduce chondrocyte death. However, mTOR feedback inhibits the activity of the PI3K/Akt pathway and inhibition of mTOR could result in increased activity of the PI3K/Akt/NF-kB pathway. We proposed that the use of dual inhibitors of PI3K and mTOR could be a promising approach to more efficiently inhibit the PI3K/Akt pathway than rapamycin or PI3K inhibitor alone and produce better treatment outcome. J. Cell. Biochem. 114: 245249, 2013. (c) 2012 Wiley Periodicals, Inc.
引用
收藏
页码:245 / 249
页数:5
相关论文
共 49 条
[1]
Cell death of chondrocytes is a combination between apoptosis and autophagy during the pathogenesis of Osteoarthritis within an experimental model [J].
Almonte-Becerril, M. ;
Navarro-Garcia, F. ;
Gonzalez-Robles, A. ;
Vega-Lopez, M. A. ;
Lavalle, C. ;
Kouri, J. B. .
APOPTOSIS, 2010, 15 (05) :631-638
[2]
Weight loss in obese people has structure-modifying effects on medial but not on lateral knee articular cartilage [J].
Anandacoomarasamy, A. ;
Leibman, S. ;
Smith, G. ;
Caterson, I. ;
Giuffre, B. ;
Fransen, M. ;
Sambrook, P. N. ;
March, L. .
ANNALS OF THE RHEUMATIC DISEASES, 2012, 71 (01) :26-32
[3]
Benderdour M, 2002, J RHEUMATOL, V29, P1262
[4]
Enhanced cleavage of type II collagen by collagenases in osteoarthritic articular cartilage [J].
Billinghurst, RC ;
Dahlberg, L ;
Ionescu, M ;
Reiner, A ;
Bourne, R ;
Rorabeck, C ;
Mitchell, P ;
Hambor, J ;
Diekmann, O ;
Tschesche, H ;
Chen, J ;
VanWart, H ;
Poole, AR .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (07) :1534-1545
[5]
Blanco FJ, 1998, ARTHRITIS RHEUM, V41, P284, DOI 10.1002/1529-0131(199802)41:2<284::AID-ART12>3.0.CO
[6]
2-T
[7]
Regulation of Autophagy in Human and Murine Cartilage Hypoxia-Inducible Factor 2 Suppresses Chondrocyte Autophagy [J].
Bohensky, Jolene ;
Terkhorn, Shawn P. ;
Freeman, Theresa A. ;
Adams, Christopher S. ;
Garcia, Joseph A. ;
Shapiro, Irving M. ;
Srinivas, Vickram .
ARTHRITIS AND RHEUMATISM, 2009, 60 (05) :1406-1415
[8]
Autophagy activation by rapamycin reduces severity of experimental osteoarthritis [J].
Carames, Beatriz ;
Hasegawa, Akihiko ;
Taniguchi, Noboru ;
Miyaki, Shigeru ;
Blanco, Francisco J. ;
Lotz, Martin .
ANNALS OF THE RHEUMATIC DISEASES, 2012, 71 (04) :575-581
[9]
Autophagy Is a Protective Mechanism in Normal Cartilage, and Its Aging-Related Loss Is Linked With Cell Death and Osteoarthritis [J].
Carames, Beatriz ;
Taniguchi, Noboru ;
Otsuki, Shuhei ;
Blanco, Francisco J. ;
Lotz, Martin .
ARTHRITIS AND RHEUMATISM, 2010, 62 (03) :791-801
[10]
Multiple signal pathways in obesity-associated cancer [J].
Chen, J. .
OBESITY REVIEWS, 2011, 12 (12) :1063-1070