PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 23272911-0 2013 Deregulation of PI3K/Akt/mTOR signaling pathways by isoflavones and its implication in cancer treatment. Isoflavones 52-63 mechanistic target of rapamycin kinase Homo sapiens 25-29 23272911-7 2013 In this review article, we discuss our current understanding of the regulation of PI3K/Akt/mTOR signaling pathways by isoflavones, which could be responsible for their observed in vitro and in vivo activity against human cancers. Isoflavones 118-129 mechanistic target of rapamycin kinase Homo sapiens 91-95 34873494-0 2021 Erratum: A preclinical report of a cobimetinib-inspired novel anticancer small-molecule scaffold of isoflavones, NSC777213, for targeting PI3K/AKT/mTOR/MEK in multiple cancers. Isoflavones 100-111 mechanistic target of rapamycin kinase Homo sapiens 147-151 19472400-0 2009 NV-128, a novel isoflavone derivative, induces caspase-independent cell death through the Akt/mammalian target of rapamycin pathway. Isoflavones 16-26 mechanistic target of rapamycin kinase Homo sapiens 94-123 20177775-0 2010 Effect of combination treatment of rapamycin and isoflavones on mTOR pathway in human glioblastoma (U87) cells. Isoflavones 49-60 mechanistic target of rapamycin kinase Homo sapiens 64-68 20177775-6 2010 In this study we investigated the effect of combination treatment of rapamycin with isoflavones such as genistein and biochanin A on mTOR pathway and activation of Akt and eIF4E in human glioblastoma (U87) cells. Isoflavones 84-95 mechanistic target of rapamycin kinase Homo sapiens 133-137 14514441-8 2003 Isoflavone metabolites also exhibited higher antioxidant activity than parent compounds in standard antioxidant (FRAP and TEAC) assays. Isoflavones 0-10 mechanistic target of rapamycin kinase Homo sapiens 113-117 34249417-0 2021 A preclinical report of a cobimetinib-inspired novel anticancer small-molecule scaffold of isoflavones, NSC777213, for targeting PI3K/AKT/mTOR/MEK in multiple cancers. Isoflavones 91-102 mechanistic target of rapamycin kinase Homo sapiens 138-142 29179444-5 2017 Western blot analysis demonstrated that the mammalian target of rapamycin (mTOR) pathway in Y79 cells was inhibited by isoflavones, with a concomitant decrease in cyclin E1, which accounted for the isoflavone-mediated G1 phase arrest. Isoflavones 119-130 mechanistic target of rapamycin kinase Homo sapiens 44-73 29179444-5 2017 Western blot analysis demonstrated that the mammalian target of rapamycin (mTOR) pathway in Y79 cells was inhibited by isoflavones, with a concomitant decrease in cyclin E1, which accounted for the isoflavone-mediated G1 phase arrest. Isoflavones 119-130 mechanistic target of rapamycin kinase Homo sapiens 75-79 29179444-5 2017 Western blot analysis demonstrated that the mammalian target of rapamycin (mTOR) pathway in Y79 cells was inhibited by isoflavones, with a concomitant decrease in cyclin E1, which accounted for the isoflavone-mediated G1 phase arrest. Isoflavones 119-129 mechanistic target of rapamycin kinase Homo sapiens 44-73 29179444-5 2017 Western blot analysis demonstrated that the mammalian target of rapamycin (mTOR) pathway in Y79 cells was inhibited by isoflavones, with a concomitant decrease in cyclin E1, which accounted for the isoflavone-mediated G1 phase arrest. Isoflavones 119-129 mechanistic target of rapamycin kinase Homo sapiens 75-79 29179444-7 2017 Together, these results illustrate that isoflavones inhibit retinoblastoma tumour growth in vitro and vivo and that inactivation of the mTOR pathway and downregulation of cyclin E1 is involved in this action. Isoflavones 40-51 mechanistic target of rapamycin kinase Homo sapiens 136-140