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Distinct inhibitory effects on mTOR signaling by ethanol and INK128 in diffuse large B-cell lymphoma.

Cell communication and signaling : CCS | 2015

The mechanistic target of rapamycin, (mTOR) kinase plays a pivotal role in controlling critical cellular growth and survival pathways, and its aberrant induction is implicated in cancer pathogenesis. Therefore, suppression of active mTOR signaling has been of great interest to researchers; several mTOR inhibitors have been discovered to date. Ethanol (EtOH), similar to pharmacologic mTOR inhibitors, has been shown to suppress the mTOR signaling pathway, though in a non-catalytic manner. Despite population studies showing that the consumption of EtOH has a protective effect against hematological malignancies, the mechanisms behind EtOH's modulation of mTOR activity in cells and its downstream consequences are largely unknown. Here we evaluated the effects of EtOH on the mTOR pathway, in comparison to the active-site mTOR inhibitor INK128, and compared translatome analysis of their downstream effects in diffuse large B-cell lymphoma (DLBCL).

Pubmed ID: 25849580 RIS Download

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: R01CA164311
  • Agency: NCI NIH HHS, United States
    Id: P30 CA134274
  • Agency: Intramural NIH HHS, United States
  • Agency: NCI NIH HHS, United States
    Id: R01 CA164311
  • Agency: BLRD VA, United States
    Id: I01 BX002990
  • Agency: NIAAA NIH HHS, United States
    Id: R01 AA017972
  • Agency: NIAAA NIH HHS, United States
    Id: R01AA017972

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