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This stress leads to suppression of forkhead box O1 (FoxO1) signaling and subsequent upregulation of thioredoxin interacting protein, inhibition of insulin and SOD-2 expression, re-expression of Neurog3, and -cell dedifferentiation and functional failure

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Melanoma cells, which contain mutated BRAF and are resistant to the BRAF inhibitor PLX4720, exhibit increased oxidative metabolism and mitochondrial dependence for survival (157)
