PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 20630498-0 2010 IL-17A stimulates the expression of inflammatory cytokines via celecoxib-blocked prostaglandin in MC3T3-E1 cells. Celecoxib 63-72 interleukin 17A Mus musculus 0-6 35159480-6 2022 MES and celecoxib reduced the inflammation level of colon tissue, as indicated by its suppression on a panel of pro-inflammatory cytokines, including interleukin (IL)-1beta, IL-17, tumor necrosis factor alpha, and interferon gamma, and a group of inflammatory proteins, including intracellular adhesion molecule 1, vascular adhesion molecule 1, matrix metalloproteinase (MMP)-2, MMP-9, MMP-13, and inducible nitric oxidase. Celecoxib 8-17 interleukin 17A Mus musculus 174-179 28433514-7 2017 Interestingly, recruitment of CD4+T cells and F4/80+ macrophages as well as BMSC transplantation induced up-regulation of Cox-2 and IL-17A gene expression levels were reverted by celecoxib administration. Celecoxib 179-188 interleukin 17A Mus musculus 132-138 28433514-9 2017 Conditioned media of rIL-17 treated J774.2 cells when supplemented to BMSCs depicted a dose-dependent increase in the number of apoptotic cells and proapoptotic protein expression that was perturbed by celecoxib or IL-17 neutralizing antibody. Celecoxib 202-211 interleukin 17A Mus musculus 22-27 28433514-11 2017 CONCLUSION: Celecoxib protects transplanted BMSCs from Cox-2/IL-17-induced inflammation and increases their engraftment, differentiation into keratinocytes and re-epithelialization thereby potentiating wound tissue repair. Celecoxib 12-21 interleukin 17A Mus musculus 61-66 20937352-0 2011 Interleukin-17A induces cathepsin K and MMP-9 expression in osteoclasts via celecoxib-blocked prostaglandin E2 in osteoblasts. Celecoxib 76-85 interleukin 17A Mus musculus 0-15 20937352-9 2011 Celecoxib, a specific inhibitor of cyclooxygenase-2 (COX-2), blocked both the IL-17A-stimulated increase in TRAP-positive multinucleated cells and the expression of cathepsin K and MMP-9. Celecoxib 0-9 interleukin 17A Mus musculus 78-84 20937352-11 2011 These results suggest that IL-17A induces the differentiation and function of osteoclasts via celecoxib-blocked prostaglandin, mainly PGE(2), in osteoblasts. Celecoxib 94-103 interleukin 17A Mus musculus 27-33 20630498-11 2010 CONCLUSION: These results suggest that IL-17A stimulates the expression of bone resorption-related inflammatory cytokines through an autocrine mechanism involving celecoxib-blocked PGs, mainly PGE(2), in osteoblasts. Celecoxib 163-172 interleukin 17A Mus musculus 39-45 20630498-8 2010 Celecoxib blocked the stimulatory effect of IL-17A on the expression of COX-2, IL-1alpha, IL-6, IL-8, and IL-11 as well as PGE(2) production, whereas it did not block TNF-alpha expression. Celecoxib 0-9 interleukin 17A Mus musculus 44-50