Macro view of microRNA function in osteoarthritis

被引:198
作者
Miyaki, Shigeru [2 ]
Asahara, Hiroshi [1 ]
机构
[1] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
[2] Hiroshima Univ Hosp, Dept Regenerat Med, Hiroshima 7348551, Japan
基金
新加坡国家研究基金会; 日本科学技术振兴机构;
关键词
HUMAN ARTICULAR CHONDROCYTES; RHEUMATOID-ARTHRITIS; CARTILAGE HOMEOSTASIS; MICROPROCESSOR COMPLEX; MONONUCLEAR-CELLS; MOLECULAR TARGETS; SYNOVIAL TISSUE; UNITED-STATES; IN-VITRO; EXPRESSION;
D O I
10.1038/nrrheum.2012.128
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Osteoarthritis (OA), the most common musculoskeletal disorder, is complex, multifaceted, and characterized by degradation of articular cartilage and alterations in other joint tissues. Although some pathogenic pathways have been characterized, current knowledge is incomplete and effective approaches to the prevention or treatment of OA are lacking. Understanding novel molecular mechanisms that are involved in the maintenance and destruction of articular cartilage, including extracellular regulators and intracellular signalling mechanisms in joint cells that control cartilage homeostasis, has the potential to identify new therapeutic targets in OA. MicroRNAs control tissue development and homeostasis by fine-tuning gene expression, with expression patterns specific to tissues and developmental stages, and are increasingly implicated in the pathogenesis of complex diseases such as cancer and cardiovascular disorders. The emergent roles of microRNAs in cartilage homeostasis and OA pathogenesis are summarized in this Review, alongside potential clinical applications.
引用
收藏
页码:543 / 552
页数:10
相关论文
共 95 条
  • [31] Integrative MicroRNA and Proteomic Approaches Identify Novel Osteoarthritis Genes and Their Collaborative Metabolic and Inflammatory Networks
    Iliopoulos, Dimitrios
    Malizos, Konstantinos N.
    Oikonomou, Pagona
    Tsezou, Aspasia
    [J]. PLOS ONE, 2008, 3 (11):
  • [32] Jazbutyte V., AGE DORDR IN PRESS
  • [33] The identification of differentially expressed microRNA in osteoarthritic tissue that modulate the production of TNF-α and MMP13
    Jones, S. W.
    Watkins, G.
    Le Good, N.
    Roberts, S.
    Murphy, C. L.
    Brockbank, S. M. V.
    Needham, M. R. C.
    Read, S. J.
    Newham, P.
    [J]. OSTEOARTHRITIS AND CARTILAGE, 2009, 17 (04) : 464 - 472
  • [34] New molecular targets for the treatment of osteoarthritis
    Jose Alcaraz, Maria
    Megias, Javier
    Garcia-Arnandis, Isabel
    Clerigues, Victoria
    Isabel Guillen, Maria
    [J]. BIOCHEMICAL PHARMACOLOGY, 2010, 80 (01) : 13 - 21
  • [35] Dicer-deficient mouse embryonic stem cells are defective in differentiation and centromeric silencing
    Kanellopoulou, C
    Muljo, SA
    Kung, AL
    Ganesan, S
    Drapkin, R
    Jenuwein, T
    Livingston, DM
    Rajewsky, K
    [J]. GENES & DEVELOPMENT, 2005, 19 (04) : 489 - 501
  • [36] Dicer-dependent pathways regulate chondrocyte proliferation and differentiation
    Kobayashi, Tatsuya
    Lu, Jun
    Cobb, Bradley S.
    Rodda, Stephen J.
    McMahon, Andrew P.
    Schipani, Ernestina
    Merkenschlager, Matthias
    Kronenberg, Henry M.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (06) : 1949 - 1954
  • [37] Circulating microRNA in body fluid: a new potential biomarker for cancer diagnosis and prognosis
    Kosaka, Nobuyoshi
    Iguchi, Haruhisa
    Ochiya, Takahiro
    [J]. CANCER SCIENCE, 2010, 101 (10): : 2087 - 2092
  • [38] Kosaka Nobuyoshi, 2010, Silence, V1, P7, DOI 10.1186/1758-907X-1-7
  • [39] Therapeutic Silencing of MicroRNA-122 in Primates with Chronic Hepatitis C Virus Infection
    Lanford, Robert E.
    Hildebrandt-Eriksen, Elisabeth S.
    Petri, Andreas
    Persson, Robert
    Lindow, Morten
    Munk, Martin E.
    Kauppinen, Sakari
    Orum, Henrik
    [J]. SCIENCE, 2010, 327 (5962) : 198 - 201
  • [40] Lawrence RC, 2008, ARTHRITIS RHEUM, V58, P26, DOI 10.1002/art.23176