Korean J Intern Med.
1999 Jan;14(1):59-65.
Expression of p53 protein in rheumatoid arthritis synovium. An immunohistochemical analysis
- Affiliations
-
- 1Division of Rheumatology , Department of Internal Medicine, College of Medicine, Korea University, Seoul, Korea.
- 2Department of Anatomical Pathology, College of Medicine, Korea University, Seoul, Korea.
Abstract
OBJECTIVES
Mutation of p53 may play a role in manifestation of rheumatoid
arthritis synovium, but several studies on p53 expression in synovial tissues of
rheumatoid arthritis showed conflicting results. We investigated the amount and
pattern of p53 positive cells in rheumatoid arthritis synovium, in comparison
with osteoarthritis synovium, by using immunohistochemistry with two other
monoclonal antibodies for p53. METHODS: Synovial tissues from 9 patients with
rheumatoid arthritis and 5 patients with osteoarthritis were examined for p53
expression by immunohistochemistry with 2 monoclonal antibodies for p53, DO-1
and DO-7. Histologic features of inflammation were also scored and compared with
p53 expression. RESULTS: There was no significant difference between
inflammatory scores in both groups. In the synovial tissues of rheumatoid
arthritis patients, p53 positive cells were detected in 3 out of 9 samples(33%)
and p53 expressions were restricted to inflammatory mononuclear cells, but
synovial lining cells, subsynovial fibroblast-like cells and vascular
endothelial cells were p53 negative. p53 expressions in osteoarthritis synovial
tissues as control were observed in 2 out of 5 samples(40%) and the amount and
pattern of p53 positive cells were comparable to those seen in rheumatoid
arthritis synovial tissues. There was no demonstrable correlation between the
synovial tissues of both groups with respect to inflammation scores and
expression of p53 protein. CONCLUSION: Our findings suggest that altered p53
expression may not play a significant role in the manifestation of rheumatoid
arthritis synovium. However these data need to be strengthened by increasing the
number of samples and molecular biology approaches.