PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 30320903-6 2019 Cotreatment of either purvalanol or roscovitine with ERK1/2 inhibitor, U0126, synergistically suppressed cell proliferation, and induced apoptotic action. purvalanol B 22-32 mitogen-activated protein kinase 3 Homo sapiens 53-59 30320903-8 2019 This study provides biological evidence about purvalanol and roscovitine have apoptotic and antimetastatic effects via MAPK signaling on prostate cancer cell by activation of GSK3beta signaling and inhibition of phosphoinositide-3-kinase/AKT (PI3K/AKT) pathways involved in the EMT process. purvalanol B 46-56 mitogen-activated protein kinase 3 Homo sapiens 119-123 12226745-6 2002 In addition to CDK1, p42/p44 MAPK were found to be two major purvalanol-interacting proteins in five different mammalian cell lines (CCL39, PC12, HBL100, MCF-7 and Jurkat cells), suggesting the generality of the purvalanol/p42/p44 MAPK interaction. purvalanol B 61-71 mitogen-activated protein kinase 3 Homo sapiens 25-33 12226745-6 2002 In addition to CDK1, p42/p44 MAPK were found to be two major purvalanol-interacting proteins in five different mammalian cell lines (CCL39, PC12, HBL100, MCF-7 and Jurkat cells), suggesting the generality of the purvalanol/p42/p44 MAPK interaction. purvalanol B 61-71 mitogen-activated protein kinase 3 Homo sapiens 29-33 12226745-12 2002 When cells were treated with purvalanol, p42/p44 MAPK and CDK1 activities were inhibited in a dose-dependent manner. purvalanol B 29-39 mitogen-activated protein kinase 3 Homo sapiens 49-53 12226745-13 2002 Furthermore, purvalanol inhibited the nuclear accumulation of p42/p44 MAPK, an event dependent on the catalytic activity of these kinases. purvalanol B 13-23 mitogen-activated protein kinase 3 Homo sapiens 66-74 12226745-14 2002 We conclude that the anti-proliferative properties of purvalanol are mediated by inhibition of both p42/p44 MAPK and CDKs. purvalanol B 54-64 mitogen-activated protein kinase 3 Homo sapiens 108-112