Gene expression analysis in RA: towards personalized medicine

被引:49
作者
Burska, A. N. [1 ,2 ]
Roget, K. [3 ]
Blits, M. [4 ]
Gomez, L. Soto [5 ]
van de Loo, F. [6 ]
Hazelwood, L. D. [7 ]
Verweij, C. L. [4 ]
Rowe, A. [8 ]
Goulielmos, G. N. [9 ]
van Baarsen, L. G. M. [10 ]
Ponchel, F. [1 ,2 ]
机构
[1] Univ Leeds, Leeds Inst Rheumat & Musculoskeletal Med, Leeds LS9 7TF, W Yorkshire, England
[2] Univ Leeds, Leeds Musculoskeletal Biomediacal Res Unit, Leeds LS9 7TF, W Yorkshire, England
[3] TcLand Express, Huningue, France
[4] Vrije Univ Amsterdam, Med Ctr, Dept Pathol & Rheumatol, Inflammatory Dis Profiling Unit, Amsterdam, Netherlands
[5] Univ Leeds, Sch Law, Leeds LS9 7TF, W Yorkshire, England
[6] Nijmegen Ctr Mol Life Sci, Dept Rheumatol Res & Adv Therapeut, Nijmegen, Netherlands
[7] Univ Leeds, Sch Mol & Cellular Biol, Fac Biol Sci, Leeds LS9 7TF, W Yorkshire, England
[8] Janssen Res & Dev, High Wycombe, Bucks, England
[9] Univ Crete, Mol Med & Human Genet Sect, Dept Med, Iraklion, Greece
[10] Univ Amsterdam, Acad Med Ctr, NL-1105 AZ Amsterdam, Netherlands
关键词
arthritis; gene expression; pharmacological biomarker; rheumatoid; RHEUMATOID-ARTHRITIS PATIENTS; BLOOD MONONUCLEAR-CELLS; SYNOVIAL TISSUE HETEROGENEITY; CYCLIC CITRULLINATED PEPTIDE; FIBROBLAST-LIKE SYNOVIOCYTES; ACUTE LYMPHOBLASTIC-LEUKEMIA; EARLY INFLAMMATORY ARTHRITIS; I INTERFERON SIGNATURE; MOLECULAR GRADE INDEX; NECROSIS FACTOR-ALPHA;
D O I
10.1038/tpj.2013.48
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gene expression has recently been at the forefront of advance in personalized medicine, notably in the field of cancer and transplantation, providing a rational for a similar approach in rheumatoid arthritis (RA). RA is a prototypic inflammatory autoimmune disease with a poorly understood etiopathogenesis. Inflammation is the main feature of RA; however, many biological processes are involved at different stages of the disease. Gene expression signatures offer management tools to meet the current needs for personalization of RA patient's care. This review analyses currently available information with respect to RA diagnostic, prognostic and prediction of response to therapy with a view to highlight the abundance of data, whose comparison is often inconclusive due to the mixed use of material source, experimental methodologies and analysis tools, reinforcing the need for harmonization if gene expression signatures are to become a useful clinical tool in personalized medicine for RA patients.
引用
收藏
页码:93 / 106
页数:14
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