Molecular Cancer Therapeutics · 2013 · 216 citations · 22 references
MedicineOncologyPharmacologyCell SignalingMetastasisMolecular OncologyAngiogenesisCancer Cell SignalingCancer ProgressionMalignant NeoplasmsMelanoma PharmacotherapySignal Transduction In CancerCancer Metastasis MechanismsEpithelial-mesenchymal Transition In CancerInvasion-metastasis CascadeMelanoma ProgressionMetastasis ModelsMetastasis PromotionMetastasis SuppressionTumor Suppressor P53
Metformin was reported to inhibit the proliferation of many cancer cells, including melanoma cells. In this report, we investigated the effect of metformin on melanoma invasion and metastasis development. Using different in vitro approaches, we found that metformin inhibits cell invasion without affecting cell migration and independently of antiproliferation action. This inhibition is correlated with modulation of expression of proteins involved in epithelial-mesenchymal transition such as Slug, Snail, SPARC, fibronectin, and N-cadherin and with inhibition of MMP-2 and MMP-9 activation. Furthermore, our data indicate that this process is dependent on activation of AMPK and tumor suppressor protein p53. Finally, we showed that metformin inhibits melanoma metastasis development in mice using extravasation and metastasis models. The presented data reinforce the fact that metformin might be a good candidate for clinical trial in melanoma treatment.
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p53 controls cancer cell invasion by inducing the MDM2-mediated degradation of Slug
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