Is GRP78/BiP a potential salivary biomarker in patients with rheumatoid arthritis?

被引:48
|
作者
Giusti, Laura [1 ]
Baldini, Chiara [2 ]
Ciregia, Federica [1 ]
Giannaccini, Gino [1 ]
Giacomelli, Camillo [2 ]
De Feo, Francesca [2 ]
Delle Sedie, Andrea [2 ]
Riente, Lucrezia [2 ]
Lucacchini, Antonio [1 ]
Bazzichi, Laura [2 ]
Bombardieri, Stefano [2 ]
机构
[1] Univ Pisa, Dept Psychiat Neurobiol Pharmacol & Biotechnol, I-56126 Pisa, Italy
[2] Univ Pisa, Rheumatol Unit, Dept Internal Med, I-56126 Pisa, Italy
关键词
78 kDa glucose-regulated protein precursor; Biomarkers; Rheumatoid arthritis; Whole saliva; STRESS-PROTEIN BIP; JUVENILE IDIOPATHIC ARTHRITIS; FLIGHT MASS-SPECTROMETRY; NECROSIS-FACTOR-ALPHA; ACID-BINDING PROTEIN; SJOGRENS-SYNDROME; T-CELLS; SYNOVIAL-FLUID; WHOLE SALIVA; ENDOPLASMIC-RETICULUM;
D O I
10.1002/prca.200900082
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Purpose: In the last few years, serum and joint synovial fluid have been extensively analyzed for the proteomic research of rheumatoid arthritis (RA) biomarkers. Nonetheless, to date, there have been no studies investigating salivary biomarkers in this condition. Therefore, aim of this study is to investigate the presence of potential biomarkers of RA in human whole saliva. Experimental design: We combined 2-DE and MS to analyze the whole saliva protein profile of 20 RA patients in comparison with 20 sex- and age-matched healthy subjects. Results: Eight salivary proteins resulted differentially expressed, namely calgranulin A, calgranulin B, apolipoprotein A-1, 6-phosphogluconate dehydrogenase, peroxiredoxin 5, epidermal fatty acid-binding protein, 78 kDa glucose-regulated protein precursor (GRP78/BiP), and 14-3-3 proteins. It is particularly interesting that chaperone GRP78/BiP showed the greatest increase in RA patients. This finding was validated by Western Blot analysis and the over-expression of GRP78/BiP appear to be distinctive of RA and drugs treatment independent. Conclusions and clinical relevance: This study provides a rationale for further studies aimed at evaluating any correlation between GRP78/BiP and different clinical/serological aspects of the disease in order to improve the diagnostic algorithms of RA.
引用
收藏
页码:315 / 324
页数:10
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