PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 18953652-3 2009 To clarify the molecular mechanism of these effects, we examined the expression of Ras/MAPK signaling pathway-related molecules in human and canine breast cancer cell lines, and found that the level of c-Raf-1 protein was reduced by 5, 10 and 20 mM of NaPA treatments, though Ras activation was maintained. Acecainide 252-256 mitogen-activated protein kinase 1 Canis lupus familiaris 87-91 18953652-3 2009 To clarify the molecular mechanism of these effects, we examined the expression of Ras/MAPK signaling pathway-related molecules in human and canine breast cancer cell lines, and found that the level of c-Raf-1 protein was reduced by 5, 10 and 20 mM of NaPA treatments, though Ras activation was maintained. Acecainide 252-256 TNF receptor associated factor 3 Homo sapiens 202-209 18953652-4 2009 Dephosphorylation of c-Raf-1 at Serine (Ser) 259, Ser 338, and Ser 621 were also seen in NaPA-treated cells. Acecainide 89-93 TNF receptor associated factor 3 Homo sapiens 21-28 18953652-7 2009 Furthermore, expression of an epithelial marker, E-cadherin, was increased by NaPA treatment. Acecainide 78-82 cadherin 1 Canis lupus familiaris 49-59 18953652-8 2009 These results suggest that one of the molecular targets of NaPA treatment was the reduction of c-Raf-1 protein, and that its reduction results in the decrease of malignant characteristics of tumor cells through blockage of the Ras/MAPK signaling pathway. Acecainide 59-63 TNF receptor associated factor 3 Homo sapiens 95-102 18953652-8 2009 These results suggest that one of the molecular targets of NaPA treatment was the reduction of c-Raf-1 protein, and that its reduction results in the decrease of malignant characteristics of tumor cells through blockage of the Ras/MAPK signaling pathway. Acecainide 59-63 mitogen-activated protein kinase 1 Canis lupus familiaris 231-235