3.4.24.17 down Curcumin dose dependently suppresses MMP-3 and -9 expression in Helicobacter pylori infected human gastric epithelial cells 718271 3.4.24.17 down Curcumin dose dependently suppresses MMP-3 and -9 expression in Helicobacter pylori infected mouse gastric tissues 718271 3.4.24.17 down dexamethasone suppression of MMP-3 gene expression 709370 3.4.24.17 down expression of MMP-3 in cartilages and synovial tissues is suppressed by the treatment of curcumin and indomethacin. Production of MMP-3 is inhibited by curcumin in tumor necrosis factor-alpha-stimulated rheumatoid arthritis fibroblast-like synoviocytes and chondrocytes in a dose-dependent manner putatively through the inhibition of PKCdelta and the JNK/c-Jun signaling pathway, overview 709685 3.4.24.17 down glycitein, i.e. 4',7-dihydroxy-6-methoxyisoflavone, a bacterial metabolite of the isoflavone glycitin, downregulates MMP-3 gene expression by inhibiting the promoter activity of MMP-3 708089 3.4.24.17 down interleukin-1Ra, dexamethasone, and TNF significantly decrease levels of all forms of MMP-3 707312 3.4.24.17 down production of MMP-3 is inhibited by curcumin in collagen-induced arthritis hind paw sections in a dose-dependent manner putatively through the inhibition of PKCdelta and the JNK/c-Jun signaling pathway, overview -, 709685 3.4.24.17 down reduced MMP-3 expression in invasive trophoblasts of patients with severe preeclampsia 710257 3.4.24.17 down stromelysin-1 is slightly downregulated in obese adipose tissue compared to non-obese adipose tissue. Expression of MMP-3 mRNA in subcutaneous and gonadal adipose tissue is affected and 3.0-3.7fold reduced by MMP-10 deficiency, but vessel size is not affected 707379 3.4.24.17 additional information lipopolysaccharide does not induce mmp-3 mRNA expression in peripheral blood samples -, 733946 3.4.24.17 up exposure of primary glial cultures to psychosine induces the expression and the production of matrix metalloproteinase-3 that mediates a morphological transformation of microglia into a multinucleated globoid cell type. But although psychosine treatment in primary purified microglial cultures moderately induces MMP-3 expression, treatment of peripheral blood or purified macrophages with equivalent concentrations of psychosine does not induce MMP-3 expression -, 733946 3.4.24.17 up MMP-3 expression is upregulated with age, overview 708594 3.4.24.17 up MMP-3 is induced by interleukin-1beta, which, despite its effects on MMP-3 expression, fails to significantly alter invasion of SGHPL-4 cells through Matrigel-coated transwells 710257 3.4.24.17 up MMP-3 is induced in gingival fibroblasts in response to inflammatory cytokines, such as TNF and interleukin-1 709669 3.4.24.17 up MMP-3 is upregulated after stroke in brain in the infarcted tissue compared to healthy control areas, overview 709700 3.4.24.17 up serum MMP-3 is significantly elevated in ankylosing spondylitis patients with active disease 718392 3.4.24.17 up the expression of the enzyme is upregulated in Dengue virus-infected RAW264.7 cells 735131 3.4.24.17 up TNF-alpha and IL-1beta stimulate production of MMPs through the activation of mitogen-activated protein kinases, NF-kappaB and AP-1 709685 3.4.24.17 up TNF-alpha and interleukin-1beta act synergistically to drive MMP-3 secretion. NF-kappaB and AP-1 c-Jun/FosB heterodimers regulate CoMTb-induced MMP-3 secretion. NF-kappaB p65 and AP-1 c-Jun subunits are upregulated in biopsy granulomas from patients with cerebral tuberculosis. CoMTb upregulates MMP-3 gene expression and secretion in microglia 709370