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Metformin and trametinib have synergistic effects on cell viability and tumor growth in NRAS mutant cancer.

Oncotarget | 2015

Attempts to directly block the mutant neuroblastoma rat sarcoma oncogene (NRAS) protein, a driving mutation in many cancer types, have been unsuccessful. Current treatments focus on inhibition of different components of NRAS' two main downstream cascades: PI3K/AKT/mTOR and MAPK. Here we test a novel dual therapy combination of metformin and trametinib on a panel of 16 NRAS mutant cell lines, including melanoma cells, melanoma cells with acquired trametinib resistance, lung cancer and neuroblastoma cells. We show that both of the main downstream cascades of NRAS can be blocked by this combination: metformin indirectly inhibits the PI3K/AKT/mTOR pathway and trametinib directly impedes the MAPK pathway. This dual therapy synergistically reduced cell viability in vitro and xenograft tumor growth in vivo. We conclude that metformin and trametinib combinations are effective in preclinical models and may be a possible option for treatment of NRAS mutant cancers.

Pubmed ID: 25504439 RIS Download

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: K08 CA155035
  • Agency: NCI NIH HHS, United States
    Id: K08CA155035

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SK-MEL-2 (tool)

RRID:CVCL_0069

Cell line SK-MEL-2 is a Cancer cell line with a species of origin Homo sapiens (Human)

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SK-N-AS (tool)

RRID:CVCL_1700

Cell line SK-N-AS is a Cancer cell line with a species of origin Homo sapiens (Human)

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CrTac:NCr-Foxn1nu (tool)

RRID:IMSR_TAC:ncrnu

Mus musculus with name CrTac:NCr-Foxn1nu from IMSR.

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