INT26314
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Serum matrix metalloproteinase-3, a parameter of synovial inflammation, was significantly increased in PMR patients. | |||||||||||||||
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The increased protein levels of MMP-1 and MMP-3 were also reduced by 1000 microg/ml HA. | |||||||||||||||
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Spontaneous parturition at term and preterm is associated with significant increase in amniotic fluid concentrations of MMP-3, but not MMP-1 (Maymon et al., 2000; Park et al., 2003). | |||||||||||||||
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Prostaglandin E2, for instance, induces activation of MMP-3, but does not affect MMP-3 total protein in the rat cervix (Chien et al., 2005). | |||||||||||||||
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Activated MMP1, MMP3 and latent forms of MMP2 and MMP9 are regulated and inhibited by endogenous proteins known as tissue inhibitors of metalloproteinase TIMP1 and TIMP2 [17]. | |||||||||||||||
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They found elevated concentrations of MMP2 and MMP3 in patients with advanced TCC of the bladder (pT2-T4, N+, M+) in comparison to the serum of patients with superficial tumors (Ta-T1, N0, M0). | |||||||||||||||
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Activated MMP1, MMP3, and latent forms of MMP2 and MMP9 bind to and are inhibited by TIMP1 and TIMP2. | |||||||||||||||
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CONCLUSION: MMP-3 is significantly increased in patients with active AS but fails to correlate significantly with conventional variables used to assess disease activity. | |||||||||||||||
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The MMP-3 level in the placebo group remained virtually unchanged at day 90 compared with baseline.
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One patient with septic arthritis showed a fivefold peak increase in joint fluid aggrecan fragment concentrations, while the concentration of matrix metalloproteinase-3 increased 100-fold. | |||||||||||||||
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Their studies revealed further elevated MMP2, MMP3, and TIMP2 concentrations from patients after tumour resection, which might function as a predictive value for early detection of tumour recurrence [20,40]. | |||||||||||||||
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However, changes in both MMP3 and MMP13 gene expression are rapid, dramatic, sustained, and changing during at least the first 48 h of unloaded culture. | |||||||||||||||
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However, cytokines are known to stimulate the production of MMPs (Ito et al., 1991; Imada et al., 1997a, b; Oner et al., 2008), so it would be logical to expect an elevation of MMP-1 and MMP-3 levels when there is an increased secretion of IL-8. | |||||||||||||||
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Nimesulide significantly reduced the serum levels of both HA and MMP-3, whereas ibuprofen increased moderately but significantly the serum concentrations of MMP-3 and had no effect on the serum concentrations of HA. | |||||||||||||||
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These cytokines act in various ways in the pathogenesis of OA such as inhibition of synthesis of type 2 (articular) cartilage and activation of catabolic metalloproteases including MMP-3 which plays a critical role in cartilage degradation 44,45. | |||||||||||||||
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Serum MMP-3 levels were significantly higher in the patients than in the controls (4.71 vs. 2.79 ng/ml, P=0.04); levels were also higher for cathepsin K (6.4 vs. 3.6 pg/ml) and IL-17 (60.4 vs. 32 pg/ml), but the differences were not statistically significant. | |||||||||||||||
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In the present study, supernatant MMP levels did not demonstrate any significant differences in response to PHT and HPPH alone at either dose compared to untreated macrophage cultures although we noted a trend for higher levels of MMP-1 and MMP-3. | |||||||||||||||
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increased mRNAs for catabolic factors MMP-1 and MMP-3. | |||||||||||||||
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Tiaprofenic acid induced in vitro a concomitant increase in PLA2 and a decrease in proteoglycanase activity. | |||||||||||||||
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One interesting finding of this study is that preterm and term cervical fibroblasts show different secretion patterns of IL-8, MMP-1 and MMP-3, where IL-8 and MMP-1 are secreted at higher levels in preterm and MMP-3 in term cervical fibroblasts. | |||||||||||||||
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