Expression profiling based on graph-clustering approach to determine osteoarthritis related pathway

被引:0
作者
Zhang, B. [1 ]
Xie, Q. -G. [1 ]
Quan, Yi [1 ]
Pan, X. -M. [1 ]
机构
[1] Chengdu Mil Gen Hosp, Dept Orthoped, Chengdu, Peoples R China
关键词
Osteoarthritis; Graph-cluster; Molecular markers; RHEUMATOID-ARTHRITIS; PATHOGENESIS; CARTILAGE; PROGRESS; BIOLOGY; PROTEIN; TARGET; CELLS; A20;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BACKGROUND: Osteoarthritis (OA) is the most common disease of joints in adults around the world. Current available drugs to treat osteoarthritis are predominantly directed towards the symptomatic relief of pain and inflammation but they do little to reduce joint destruction. Effective prevention of the structural damage must be a key objective of new therapeutic approaches. Therefore, it is worthwhile to search for important molecular markers that hold great promise for further treatment of patients with osteoarthritis. AIM: In this study, we used a graph-clustering approach to identify gene expression profiles that distinguish OA patients from normal samples. MATERIALS AND METHODS: We performed a comprehensive gene level assessment of osteoarthritis using five osteoarthritis samples and five normal samples graph-clustering approach. RESULTS: The results showed that TNFAIP3, ATF3, PPARG, etc, have related with osteoarthritis. Besides, we further mined the underlying molecular mechanism within these differently genes. CONCLUSIONS: The results indicated tyrosine metabolism pathway and cell cycle pathway were two significant pathways, and there was evident to demonstrate them based on previous reports. We hope to provide insights into the development of novel therapeutic targets and pathways.
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收藏
页码:2097 / 2102
页数:6
相关论文
共 26 条
[1]   Developments in the scientific understanding of osteoarthritis [J].
Abramson, Steven B. ;
Attur, Mukundan .
ARTHRITIS RESEARCH & THERAPY, 2009, 11 (03)
[2]   Development and implementation of an algorithm for detection of protein complexes in large interaction networks [J].
Altaf-Ul-Amin, Md ;
Shinbo, Yoko ;
Mihara, Kenji ;
Kurokawa, Ken ;
Kanaya, Shigehiko .
BMC BIOINFORMATICS, 2006, 7 (1)
[3]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[4]   Molecular mechanisms of cartilage remodelling in osteoarthritis [J].
Bertrand, Jessica ;
Cromme, Christoph ;
Umlauf, Daniel ;
Frank, Svetlana ;
Pap, Thomas .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2010, 42 (10) :1594-1601
[5]   Catecholamine-producing cells in the synovial tissue during arthritis: modulation of sympathetic neurotransmitters as new therapeutic target [J].
Capellino, Silvia ;
Cosentino, Marco ;
Wolff, Christine ;
Schmidt, Martin ;
Grifka, Joachim ;
Straub, Rainer H. .
ANNALS OF THE RHEUMATIC DISEASES, 2010, 69 (10) :1853-1860
[6]   Gene expression microarray analysis in cancer biology, pharmacology, and drug development: progress and potential [J].
Clarke, PA ;
Poele, RT ;
Wooster, R ;
Workman, P .
BIOCHEMICAL PHARMACOLOGY, 2001, 62 (10) :1311-1336
[7]  
Elsby LM, 2010, CLIN EXP RHEUMATOL, V28, P708
[8]   Peroxisome proliferator-activated receptor gamma in osteoarthritis [J].
Fahmi, Hassan ;
Martel-Pelletier, Johanne ;
Pelletier, Jean-Pierre ;
Kapoor, Mohit .
MODERN RHEUMATOLOGY, 2011, 21 (01) :1-9
[9]  
Flatmark T, 2000, ACTA PHYSIOL SCAND, V168, P1
[10]   Metabolomic correlation-network modules in Arabidopsis based on a graph-clustering approach [J].
Fukushima, Atsushi ;
Kusano, Miyako ;
Redestig, Henning ;
Arita, Masanori ;
Saito, Kazuki .
BMC SYSTEMS BIOLOGY, 2011, 5