Skip to main content
Download PDF

p53tumor suppressor gene mutations in fibroblast-like synoviocytes from erosion synovium and non-erosion synovium in rheumatoid arthritis

Arthritis Res Ther volume 7, Article number: R12 (2004) Cite this article

Abstract

Abnormalities in the p53 tumor suppressor gene have been detected in rheumatoid arthritis (RA) and could contribute to the pathogenesis of chronic disease. To determine whether synoviocytes from invasive synovium in RA have an increased number of mutations compared with non-erosion synoviocytes, p53 cDNA subclones from fibroblast-like synoviocytes (FLS) derived from erosion and non-erosion sites of the same synovium were examined in patients requiring total joint replacement. Ten erosion FLS lines and nine non-erosion FLS lines were established from nine patients with RA. Exons 5–10 from 209 p53 subclones were sequenced (114 from erosion FLS, 95 from non-erosion FLS). Sixty percent of RA FLS cell lines and 8.6% of the p53 subclones isolated from FLS contained p53 mutations. No significant differences were observed between the erosion and non-erosion FLS with regard to the frequency or type of p53 mutation. The majority of the mutations were missense transition mutations, which are characteristic of oxidative damage. In addition, paired intact RA synovium and cultured FLS from the same joints were evaluated for p53 mutations. Matched synovium and cultured synoviocytes contained p53 mutations, although there was no overlap in the specific mutations identified in the paired samples. Clusters of p53 mutations in subclones were detected in some FLS, including one in codon 249, which is a well-recognized 'hot spot' associated with cancer. Our data are consistent with the hypothesis that p53 mutations are randomly induced by genotoxic exposure in small numbers of RA synoviocytes localized to erosion and non-erosion regions of RA synovium. The determining factor for invasiveness might be proximity to bone or cartilage rather than the presence of a p53 mutation.

Introduction

Rheumatoid arthritis (RA) is a chronic inflammatory disease characterized by synovial tissue proliferation with progressive joint destruction. The etiology of RA remains unknown, but many factors, including autoimmunity, cytokines and genetic factors, participate in its pathogenesis [1, 2]. Although inflammation and joint destruction can be intimately related, the two processes might also be independent in some circumstances [3, 4]. This observation might be explained, at least in part, by autonomous behavior by fibroblast-like synoviocytes (FLS) [5]. These cells exhibit some features of transformation in RA, including loss of contact inhibition, anchorage-independent growth, oncogene activation, autonomous invasion into cartilage and somatic gene mutations [4, 6–9]. One potential gene that might contribute to this phenotype is the p53 tumor suppressor gene, which plays a critical role in cell-cycle regulation, DNA repair, senescence, genomic stability and apoptosis [10]. p53 is expressed in many inflammatory and autoimmune diseases [11–13], and it may serve a protective function by suppressing cytokine production and matrix destruction [14, 15]. For instance, mice lacking the p53 gene have significantly greater joint destruction compared with wild-type controls in the collagen-induced arthritis model [16].

The function of p53 can be altered through somatic mutations in both neoplasia and non-malignant conditions such as ulcerative colitis, sun-exposed skin and chronic RA [8, 17, 18]. The mutations in RA synovium reside primarily in the intimal lining and have also been identified in cultured FLS, which are thought to originate from this region [8, 9]. p53 sequencing studies in RA have until now focused on synoviocytes derived from non-erosion regions of the synovium that are readily obtained at the time of joint replacement surgery. Because some reports suggest that monoclonal expansion and oligoclonal expansion of synoviocytes occur at sites of invasion [19], we evaluated the relative frequency of p53 mutations in FLS in paired erosion and non-erosion synoviocytes from the same patients. Our data suggest that mutations are present in both regions and that the tendency to invade may be related to proximity to the extracellar matrix.

Materials and methods

Synovial tissues and preparation of FLS

Synovial tissue samples were collected with informed consent at the time of joint replacement from patients with RA. The diagnosis of RA conformed to the 1987 revised American College of Rheumatology criteria [20]. Separate samples were obtained, at the University of Toronto, from within erosions at the periphery of the articular surface and from non-erosion sites collected from the intracapsular non-articular surface. Erosion FLS lines and non-erosion FLS lines were then prepared from each patient.

FLS cell lines were established as previously described [21]. Briefly, tissues were minced by sterilized scissors, and were incubated with 1 mg/ml collagenase in serum-free DMEM for 2 hours at 37°C, were filtered through a nylon mesh, were extensively washed, and were cultured in DMEM containing 10% fetal calf serum, 2 mmol/l glutamine, 50 μg/ml gentamicin, 100 U/ml penicillin, and 100 μg/ml streptomycin, in a humidified 5% CO2 atmosphere. After overnight culture, cells were trypsinized, split in a 1:3 ratio, and were recultured in medium. FLS from passages 5–8 were used in these experiments, during which time they represented a homogeneous population of FLS (< 1% CD 11b, < 1% phagocytic, and < 1% Fc-gamma RII receptor-positive). A second set of FLS samples obtained from the University of California at San Diego were obtained with a matched sample of synovium, which was embedded in TissueTek OCT compound (Miles Diagnostics, Elkhart, IN, USA), snap frozen, and stored at -80°C until use. Frozen tissues with approximate area of 10 mm2 were cut into 10 μl sections at the time of PCR analysis for p53 mutations.

Production of immunoreactive MMP-1

FLS were cultured to near confluence in six-well tissue culture plates (Falcon, Bedford, MA, USA). IL-1β (3 ng/ml) or medium was added to the wells and was incubated for 72 hours at 37°C in a humidified 5% CO2 atmosphere. Supernatants were collected and MMP-1 concentrations were determined by ELISA according to the manufacturer's instructions (Total MMP1Biotrak; Amersham Biosciences, Piscataway, NJ, USA) [22].

Statistical analysis

Comparisons between two groups were analyzed by the Wilcoxon signed rank test. P < 0.05 was considered significant.

Results

p53mutations in erosion FLS and non-erosion FLS

To determine whether invasive synovium in RA has an increased number of mutations, p53 cDNA subclones from FLS derived from erosion sites and non-erosion sites were examined. Ten erosion FLS lines and nine non-erosion FLS lines were established from nine patients with RA (two erosion lines and one non-erosion line were examined in one patient). A total of 209 p53 subclones were subjected to sequence analysis (114 from erosion FLS, 95 from non-erosion FLS), and p53 exons 5–10 were examined. As shown in Table 1, p53 mutations were identified in 11 out of 19 FLS lines (four of 10 erosion FLS lines, and seven of nine non-erosion FLS lines). Eighteen subclones out of the total 209 (8.6%) contained mutations. There were no significant differences in the frequency of p53 mutations between erosion FLS and non-erosion FLS (7.9% and 9.5%, respectively). Nested PCR was required for one of the FLS lines (RA4 non-erosion FLS line). The rate of mutation with this line was similar to the other erosion and non-erosion FLS.

Table 1 p53 mutations in matched erosion fibroblast-like synoviocytes (FLS) and non-erosion FLS from rheumatoid arthritis(RA) patients
Full size table

As in previous reports [8, 9, 23], most p53 mutations (eight of nine in erosion FLS and eight of nine in non-erosion FLS) were transition mutations (i.e. G>A or C>T), which are characteristic of mutations caused by oxidative damage [24, 25], and no transversion mutations (i.e. G>T, A>T, C>A, C>G) were seen (see Fig. 1 for the pooled data). One single base deletion and one multinucleotide insertion were detected. The majority of p53 mutations (78%) were missense (see Fig. 1 for pooled data). Most of the mutations were identified in a single subclone, although multiple copies of one mutation in codon 321 AAA to GAA were observed in an erosion FLS line. These data suggest that the frequency and types of mutations are similar in FLS isolated from either sites of erosion or from regions that are not invading into bone or cartilage.

Figure 1
figure 1

Types of p53 mutations in rheumatoid arthritis fibroblast-like synoviocytes (FLS). Because no differences were observed between erosion FLS and non-erosion FLS (see Table 1), results were pooled.

Full size image

MMP-1 expression in erosion and non-erosion FLS

Two matched erosion and non-erosion FLS lines were also evaluated for medium-stimulated and IL-1β-stimulated collagenase gene expression (MMP-1). There were no differences between the erosion or non-erosion samples with regard to either basal or cytokine-stimulated MMP-1 protein concentrations in the culture supernatants (basal, 5.5 ± 1.2 ng/ml; IL-1 stimulated, 24.4 ± 3.2 ng/ml).

p53mutations in matched RA FLS and synovial tissue samples

After evaluating the matched FLS lines, we then examined the mutations in whole RA synovium and FLS isolated from the same joint. The matched erosion and non-erosion synovia from the preceding analysis were not available, so subclones from four additional paired RA FLS and synovial tissues from non-erosion regions were sequenced for p53 mutations (see Table 2). Mutations were detected in 12 of the 43 p53 subclones from RA FLS (28%), and in five of 46 subclones from the paired RA synovial tissues (11%). The relatively higher percentage of mutations in this limited number of lines compared with those presented in Table 1 is within the range observed for RA FLS in other studies. A few of the subclones contained two mutations (two of the RA FLS subclones, and one of the RA tissue subclones). Distinct patterns were found in the RA FLS compared with the paired tissue p53 subclones (see Table 2), although the frequency of mutations was somewhat higher in these samples compared with those presented in Table 1 and previous reports [8, 9, 23].

Table 2 p53 mutations in paired rheumatoid arthritis (RA) fibroblast-like synoviocytes and synovial tissue samples
Full size table

Mutation analysis of FLS revealed eight transitions, three transversions, and three deletions among 14 mutations in RA FLS. Of the base changes, 11 were missense and three were silent (Table 2). The RA tissue samples had five transition mutations (four A>G, one C>T) and one transversion mutation (G>T), with four mutations identified as missense and two as silent. Nested PCR was required for two FLS lines, RA11 and RA12 FLS, and these results were similar to the cell lines that did not require nested PCR. RA13 synovial tissue had no mutations identified despite the use of nested PCR, indicating the fidelity of this process.

Interestingly, FLS from one patient had multiple subclones containing a mutation at codon 249 (AGG>GGG [Arg>Gly]) (see Table 2). Codon 249 missense mutations have been detected frequently in malignant tissues [26, 27]. In another patient, a silent codon 213 base change (CGA>CGG [Arg>Arg]) was detected in 50% of p53 subclones from both FLS and synovial tissues. This same base change was also present in peripheral blood mononuclear cells of the patient (data not shown) and probably represents a known p53 germline polymorphism [28].

Discussion

The aggressive nature of RA synovium and the ability of cultured synoviocytes to invade autonomously in cartilage suggest that these cells might be permanently altered or imprinted by their sojourn through the rheumatoid joint [4, 5]. Additional data evaluating expression of X-linked genes indicate that oligoclonal or monoclonal expansion of synoviocytes can occur in chronically inflamed rheumatoid synovial tissue, especially at sites of erosions [19]. More recently, we showed that islands of cells expressing mutant p53 genes are present in the rheumatoid synovial intimal lining and that these regions produce significantly higher amounts of IL-6 [9]. However, the relationship between mutations and the synovial invasion has not been systematically examined.

In the present study, we first examined paired samples of synoviocytes isolated from the erosive front of synovium and from regions not directly adherent to bone or cartilage for p53 mutations. Sixty percent of the cell lines examined had mutations, and 8.6% of the subclones isolated from either site contained mutations. No significant differences were observed between erosion and non-erosion FLS with regard to the frequency or type of mutation. Previous reports describe p53 base changes in 15–50% of RA FLS lines, with a frequency of mutations within the p53 cDNA pool varying from 0% to 30% [8, 23, 29]. The broad range might relate to the methods used to identify mutations, some of which are less sensitive (e.g. single-strand conformation polymorphism), or may be due to the evaluation of different numbers of exons. Other investigators failed to find mutations, perhaps because the experiments focused on sequencing the unfractionated p53 cDNA pool rather than subclones, on evaluation of less severe disease, or on sequencing a limited number of subclones [30, 31].

The mutations observed in this study are mainly transition missense base changes, as previously described [8, 9, 23]. These are characteristic of oxidative deamination by nitric oxide or oxygen radicals [24, 25] and are consistent with the hypothesis that the p53 mutations are caused by oxidative stress in the inflammatory environment, although this still has not been proven [32]. Relaxation of the DNA mismatch repair mechanisms in synoviocytes also probably contributes to susceptibility to DNA damage. For instance, suppression of hMSH6 expression in RA synovium has been associated with synovial microsatellite instability [33]. The majority of mutations in the present study were only identified in individual subclones. However, multiple copies were detected in the sequenced subclones from three patients. One of these at codon 249 is a well-recognized 'hot spot' associated with lung cancer and hepatocellular carcinoma [26, 27]. Inazuka and colleagues previously identified another 'hot spot' codon 245 transition mutation in RA FLS lines from two patients [23]. Table 3 summarizes p53 mutation clusters (i.e. detected in more than one subclone) in the present study and in the literature in cultured RA FLS or synovial tissue. More than 90% of the repeat p53 mutations are missense and have been frequently detected in malignant tissues.

Table 3 p53 mutation clusters identified in greater than one subclone isolated from rheumatoid arthritis (RA) fibroblast-like synoviocytes (FLS) or from synovial tissue
Full size table

Nishioka and colleagues demonstrated oligoclonal expansion or monoclonal expansion of synoviocytes at the sites of erosion in RA [19]. Furthermore, p53 expression tends to be greatest at sites of invasion in the severe combined immunodeficiency mouse model where cultured FLS erode into cartilage explants [34]. We expected to see an increased number of mutations at these sites as well. However, there were no differences between matched erosion and non-erosion FLS with regard to the number or types of p53 mutations. The mutations in very late stage of disease are therefore equally abundant in all regions of the rheumatoid synovium. Although they are clearly present at the invasive front, which might contribute to local tissue destruction, they are not over-represented compared with other sites that have been exposed to the genotoxic environment for the same period of time. The lack of association between invasion into bone and p53 mutations is consistent with recent data suggesting that osteoclasts, rather than synoviocytes, are the primary mediators of bone erosions [35]. FLS might play a more important role in cartilage damage through the elaboration of proteolytic enzymes and cytokines, which are increased in cells lacking functional p53 protein. Mutations in erosion had unique sequences when compared with the paired non-erosion mutations from the same patient, which may not be surprising given the results of microdissection studies demonstrating multiple independent islands of mutant cells rather than diffuse monoclonal expansion [9].

In addition to studying paired erosion and non-erosion FLS, we analyzed a second set of samples where we had the opportunity to examine paired whole non-erosion synovium with FLS isolated from the same joint. Mutations were identified in the matched samples, with similar ratios of transitions and missense changes between cell lines and tissues. There was no overlap in the specific base changes. Because cells in the lining form islands with oligoclonal expansion of individual mutations, cell lines derived from a different fragment of synovium would be expected to have different mutations compared with another region. The percentage of cDNA subclones with mutations was higher in the FLS than in matched synovium. This is most probably because the cells bearing mutations in the intact tissue (synoviocytes in the intimal lining) represent only about 20% of the total compared with 100% of the cells in the homogeneous cell cultures.

Our data are consistent with the proposed hypothesis that p53 mutations are randomly induced by genotoxic exposure in small numbers of RA synovial lining cells in both erosion and non-erosion regions. Based on the association of these same mutations with neoplasia and our previous studies showing that these mutations can be dominant negative [36], it is reasonable to suggest that some of the p53 mutant cells in RA have selective growth advantage and thus form clusters in RA synovial tissue. Subsequently, the islands can influence cells in the environment through the elaboration of cytokines and factors that are normally suppressed by wild-type p53 (such as IL-6). A careful evaluation of erosion and non-erosion sites suggests that cells in both regions are equally likely to contain mutant cells, and that the expression of proteins related to matrix invasion, like MMP-1, was similar in the two cell populations. The determining factor for invasiveness might be proximity to bone or cartilage rather than the presence of a p53 mutation. Hence, cells directly adjacent to the matrix can potentially adhere and invade, whereas those cells in non-erosion regions would only have an indirect influence on destruction.

Conclusions

Mutations of the p53 tumor suppressor gene were present in synoviocytes isolated from both erosion and non-erosion sites in longstanding RA. Clusters of mutations can occur in RA synovium, but the abnormal clones are not unique to sites of joint destruction. The determining factor for invasiveness might be proximity to bone or cartilage rather than the presence of a p53 mutation. Hence, cells directly adjacent to the matrix can potentially adhere and invade whereas those cells in non-erosion regions would only have an indirect influence on destruction.

Abbreviations

DMEM:

Dulbecco's modified Eagle's medium

ELISA:

enzyme-linked immunosorbent assay

FLS:

fibroblast-like synoviocytes

IL:

interleukin

MMP-1:

matrix metalloproteinase-1

PCR:

polymerase chain reaction

RA:

rheumatoid arthritis

References

  1. Firestein GS: Evolving concepts of rheumatoid arthritis. Nature. 2003, 423: 356-361. 10.1038/nature01661.

    Article  CAS  PubMed  Google Scholar 

  2. Feldmann M, Maini RN, Bondeson J, Taylor P, Foxwell BM, Brennan FM: Cytokine blockade in rheumatoid arthritis. Adv Exp Med Biol. 2001, 490: 119-127.

    Article  CAS  PubMed  Google Scholar 

  3. Joosten LA, Helsen MM, Saxne T, van De Loo FA, Heinegard D, van Den Berg WB: IL-1 alpha beta blockade prevents cartilage and bone destruction in murine type II collagen-induced arthritis, whereas TNF-alpha blockade only ameliorates joint inflammation. J Immunol. 1999, 163: 5049-5055.

    CAS  PubMed  Google Scholar 

  4. Muller-Ladner U, Kriegsmann J, Franklin BN, Matsumoto S, Geiler T, Gay RE, Gay S: Synovial fibroblasts of patients with rheumatoid arthritis attach to and invade normal human cartilage when engrafted into SCID mice. Am J Pathol. 1996, 149: 1607-1615.

    PubMed Central  CAS  PubMed  Google Scholar 

  5. Firestein GS: Invasive fibroblast-like synoviocytes in rheumatoid arthritis. Passive responders or transformed aggressors?. Arthritis Rheum. 1996, 39: 1781-1790.

    Article  CAS  PubMed  Google Scholar 

  6. Lafyatis R, Remmers EF, Roberts AB, Yocum DE, Sporn MB, Wilder RL: Anchorage-independent growth of synoviocytes from arthritic and normal joints. Stimulation by exogenous platelet-derived growth factor and inhibition by transforming growth factor-beta and retinoids. J Clin Invest. 1989, 83: 1267-1276.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  7. Muller-Ladner U, Kriegsmann J, Gay RE, Gay S: Oncogenes in rheumatoid arthritis. Rheum Dis Clin North Am. 1995, 21: 675-690.

    CAS  PubMed  Google Scholar 

  8. Firestein GS, Echeverri F, Yeo M, Zvaifler NJ, Green DR: Somatic mutations in the p53 tumor suppressor gene in rheumatoid arthritis synovium. Proc Natl Acad Sci U S A. 1997, 94: 10895-10900. 10.1073/pnas.94.20.10895.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  9. Yamanishi Y, Boyle DL, Rosengren S, Green DR, Zvaifler NJ, Firestein GS: Regional analysis of p53 mutations in rheumatoid arthritis synovium. Proc Natl Acad Sci U S A. 2002, 99: 10025-10030. 10.1073/pnas.152333199.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  10. Levine AJ: p53, the cellular gatekeeper for growth and division. Cell. 1997, 88: 323-331. 10.1016/S0092-8674(00)81871-1.

    Article  CAS  PubMed  Google Scholar 

  11. Maacke H, Kessler A, Schmiegel W, Roeder C, Vogel I, Deppert W, Kalthoff H: Overexpression of p53 protein during pancreatitis. Br J Cancer. 1997, 75: 1501-1504.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  12. Firestein GS, Nguyen K, Aupperle KR, Yeo M, Boyle DL, Zvaifler NJ: Apoptosis in rheumatoid arthritis: p53 overexpression in rheumatoid arthritis synovium. Am J Pathol. 1996, 149: 2143-2151.

    PubMed Central  CAS  PubMed  Google Scholar 

  13. Tak PP, Smeets TJ, Boyle DL, Kraan MC, Shi Y, Zhuang S, Zvaifler NJ, Breedveld FC, Firestein GS: p53 overexpression in synovial tissue from patients with early and longstanding rheumatoid arthritis compared with patients with reactive arthritis and osteoarthritis. Arthritis Rheum. 1999, 42: 948-953. 10.1002/1529-0131(199905)42:5<948::AID-ANR13>3.0.CO;2-L.

    Article  CAS  PubMed  Google Scholar 

  14. Santhanam U, Ray A, Sehgal PB: Repression of the interleukin 6 gene promoter by p53 and the retinoblastoma susceptibility gene product. Proc Natl Acad Sci U S A. 1991, 88: 7605-7609.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  15. Sun Y, Sun Y, Wenger L, Rutter JL, Brinckerhoff CE, Cheung HS: p53 down-regulates human matrix metalloproteinase-1 (collagenase-1) gene expression. J Biol Chem. 1999, 274: 11535-11540. 10.1074/jbc.274.17.11535.

    Article  CAS  PubMed  Google Scholar 

  16. Yamanishi Y, Boyle DL, Pinkoski MJ, Mahboubi A, Lin T, Han Z, Zvaifler NJ, Green DR, Firestein GS: Regulation of joint destruction and inflammation by p53 in collagen-induced arthritis. Am J Pathol. 2002, 160: 123-130.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  17. Krishna M, Woda B, Savas L, Baker S, Banner B: Expression of p53 antigen in inflamed and regenerated mucosa in ulcerative colitis and Crohn's disease. Mod Pathol. 1995, 8: 654-657.

    CAS  PubMed  Google Scholar 

  18. Ling G, Persson A, Berne B, Uhlen M, Lundeberg J, Ponten F: Persistent p53 mutations in single cells from normal human skin. Am J Pathol. 2001, 159: 1247-1253.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  19. Imamura F, Aono H, Hasunuma T, Sumida T, Tateishi H, Maruo S, Nishioka K: Monoclonal expansion of synoviocytes in rheumatoid arthritis. Arthritis Rheum. 1998, 41: 1979-1986. 10.1002/1529-0131(199811)41:11<1979::AID-ART13>3.3.CO;2-3.

    Article  CAS  PubMed  Google Scholar 

  20. Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, Cooper NS, Healey LA, Kaplan SR, Liang MH, Luthra HS, et al: The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum. 1988, 31: 315-324.

    Article  CAS  PubMed  Google Scholar 

  21. Alvaro-Gracia JM, Zvaifler NJ, Firestein GS: Cytokines in chronic inflammatory arthritis. V. Mutual antagonism between interferon-gamma and tumor necrosis factor-alpha on HLA-DR expression, proliferation, collagenase production, and granulocyte macrophage colony-stimulating factor production by rheumatoid arthritis synoviocytes. J Clin Invest. 1990, 86: 1790-1798.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  22. Rosengren S, Firestein GS, Boyle DL: Measurement of inflammatory biomarkers in synovial tissue extracts by enzyme-linked immunosorbent assay. Clin Diagn Lab Immunol. 2003, 10: 1002-1010. 10.1128/CDLI.10.6.1002-1010.2003.

    PubMed Central  CAS  PubMed  Google Scholar 

  23. Inazuka M, Tahira T, Horiuchi T, Harashima S, Sawabe T, Kondo M, Miyahara H, Hayashi K: Analysis of p53 tumour suppressor gene somatic mutations in rheumatoid arthritis synovium. Rheumatology. 2000, 39: 262-266. 10.1093/rheumatology/39.3.262.

    Article  CAS  PubMed  Google Scholar 

  24. Wink DA, Kasprzak KS, Maragos CM, Elespuru RK, Misra M, Dunams TM, Cebula TA, Koch WH, Andrews AW, Allen JS, et al: DNA deaminating ability and genotoxicity of nitric oxide and its progenitors. Science. 1991, 254: 1001-1003.

    Article  CAS  PubMed  Google Scholar 

  25. Nguyen T, Brunson D, Crespi CL, Penman BW, Wishnok JS, Tannenbaum SR: DNA damage and mutation in human cells exposed to nitric oxide in vitro. Proc Natl Acad Sci U S A. 1992, 89: 3030-3034.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  26. Bressac B, Kew M, Wands J, Ozturk M: Selective G to T mutations of p53 gene in hepatocellular carcinoma from southern Africa. Nature. 1991, 350: 429-431. 10.1038/350429a0.

    Article  CAS  PubMed  Google Scholar 

  27. Puisieux A, Lim S, Groopman J, Ozturk M: Selective targeting of p53 gene mutational hotspots in human cancers by etiologically defined carcinogens. Cancer Res. 1991, 51: 6185-6189.

    CAS  PubMed  Google Scholar 

  28. Carbone D, Chiba I, Mitsudomi T: Polymorphism at codon 213 within the p53 gene. Oncogene. 1991, 6: 1691-1692.

    CAS  PubMed  Google Scholar 

  29. Reme T, Travaglio A, Gueydon E, Adla L, Jorgensen C, Sany J: Mutations of the p53 tumour suppressor gene in erosive rheumatoid synovial tissue. Clin Exp Immunol. 1998, 111: 353-358. 10.1046/j.1365-2249.1998.00508.x.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  30. Kullmann F, Judex M, Neudecker I, Lechner S, Justen HP, Green DR, Wessinghage D, Firestein GS, Gay S, Scholmerich J, Muller-Ladner U: Analysis of the p53 tumor suppressor gene in rheumatoid arthritis synovial fibroblasts. Arthritis Rheum. 1999, 42: 1594-1600. 10.1002/1529-0131(199908)42:8<1594::AID-ANR5>3.0.CO;2-#.

    Article  CAS  PubMed  Google Scholar 

  31. Kitasato H, Okamoto R, Kawai S: Absence of p53 mutation in Japanese patients with rheumatoid arthritis: comment on the article by Han et al. Arthritis Rheum. 2000, 43: 469-470. 10.1002/1529-0131(200002)43:2<469::AID-ANR34>3.0.CO;2-D.

    Article  CAS  PubMed  Google Scholar 

  32. Tak PP, Zvaifler NJ, Green DR, Firestein GS: Rheumatoid arthritis and p53: how oxidative stress might alter the course of inflammatory diseases. Immunol Today. 2000, 21: 78-82. 10.1016/S0167-5699(99)01552-2.

    Article  CAS  PubMed  Google Scholar 

  33. Lee SH, Chang DK, Goel A, Boland CR, Bugbee W, Boyle DL, Firestein GS: Microsatellite instability and suppressed DNA repair enzyme expression in rheumatoid arthritis. J Immunol. 2003, 170: 2214-2220.

    Article  CAS  PubMed  Google Scholar 

  34. Seemayer CA, Kuchen S, Neidhart M, Kuenzler P, Rihoskova V, Neumann E, Pruschy M, Aicher WK, Muller LU, Gay RE, et al: p53 in rheumatoid arthritis synovial fibroblasts at sites of invasion. Ann Rheum Dis. 2003, 62: 1139-1144. 10.1136/ard.2003.007401.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  35. Walsh NC, Gravallese EM: Bone loss in inflammatory arthritis: mechanisms and treatment strategies. Curr Opin Rheumatol. 2004, 16: 419-427. 10.1097/01.bor.0000127824.42507.68.

    Article  PubMed  Google Scholar 

  36. Han Z, Boyle DL, Shi Y, Green DR, Firestein GS: Dominant-negative p53 mutations in rheumatoid arthritis. Arthritis Rheum. 1999, 42: 1088-1092. 10.1002/1529-0131(199906)42:6<1088::AID-ANR4>3.0.CO;2-E.

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Department of Rheumatology, Hiroshima City Hospital, Hiroshima, Japan

    Yuji Yamanishi

  2. Division of Rheumatology, Allergy, and Immunology, School of Medicine, University of California at San Diego, La Jolla, California, USA

    Yuji Yamanishi, David L Boyle & Gary S Firestein

  3. La Jolla Institute of Allergy and Immunology, La Jolla, California, USA

    Douglas R Green

  4. Department of Medicine, University of Toronto, Canada

    Edward C Keystone, Alison Connor & Susan Zollman

Authors
  1. Yuji Yamanishi
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. David L Boyle
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Douglas R Green
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Edward C Keystone
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Alison Connor
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Susan Zollman
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Gary S Firestein
    View author publications

    You can also search for this author in PubMed Google Scholar

Corresponding author

Correspondence to Gary S Firestein.

Additional information

Competing interests

The author(s) declare that they have no competing interests.

Authors' contributions

Yuji Yamanishi designed and executed the study and prepared the manuscript. Edward Keystone, Alison Connor, and Susan Zollman developed erosion and non-erosion FLS. David Boyle assisted with the design of experiments and obtained UCSD clinical samples. Douglas Green evaluated and interpreted data and assisted with preparation of the manuscript. Gary Firestein supervised the project, evaluated and interpreted data, and prepared the manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Yamanishi, Y., Boyle, D.L., Green, D.R. et al. p53tumor suppressor gene mutations in fibroblast-like synoviocytes from erosion synovium and non-erosion synovium in rheumatoid arthritis. Arthritis Res Ther 7, R12 (2004). https://doi.org/10.1186/ar1448

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/ar1448

Keywords

Arthritis Research & Therapy

ISSN: 1478-6362

Contact us