PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 16600694-5 2006 The results showed that (i) aspirin, fenofibrate and clofibrate decrease significantly the MCP-1 expression and secretion in human endothelial cells; (ii) the high glucose up-regulated expression of MCP-1 in endothelial cells was significantly reduced by inhibitors of NF-kB and reactive oxygen species; (iii) all drugs notably decrease the level of the reactive oxygen species and activation of NF-kB and AP-1. Aspirin 28-35 jun proto-oncogene Mus musculus 406-410 9334204-0 1997 Inhibition of ultraviolet B-induced activator protein-1 (AP-1) activity by aspirin in AP-1-luciferase transgenic mice. Aspirin 75-82 jun proto-oncogene Mus musculus 57-61 9334204-0 1997 Inhibition of ultraviolet B-induced activator protein-1 (AP-1) activity by aspirin in AP-1-luciferase transgenic mice. Aspirin 75-82 jun proto-oncogene Mus musculus 86-90 9334204-7 1997 The topical pretreatment of mouse skin with aspirin markedly blocked the UVB-induced AP-1 transactivation in vivo. Aspirin 44-51 jun proto-oncogene Mus musculus 85-89 9092536-0 1997 Inhibition of activator protein 1 activity and neoplastic transformation by aspirin. Aspirin 76-83 jun proto-oncogene Mus musculus 14-33 9092536-5 1997 Aspirin and aspirin-like salicylates inhibited the activation of AP-1 in the same dose range as seen for the inhibition of tumor promoter-induced transformation. Aspirin 0-7 jun proto-oncogene Mus musculus 65-69 9092536-5 1997 Aspirin and aspirin-like salicylates inhibited the activation of AP-1 in the same dose range as seen for the inhibition of tumor promoter-induced transformation. Aspirin 12-19 jun proto-oncogene Mus musculus 65-69 9092536-8 1997 The inhibition effects on the activation of AP-1 activity by aspirin and aspirin-like salicylates may further explain the anti-carcinogenesis mechanism of action of these drugs. Aspirin 61-68 jun proto-oncogene Mus musculus 44-48 9092536-8 1997 The inhibition effects on the activation of AP-1 activity by aspirin and aspirin-like salicylates may further explain the anti-carcinogenesis mechanism of action of these drugs. Aspirin 73-80 jun proto-oncogene Mus musculus 44-48