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Abstract Increased glucose uptake and metabolism is a prominent phenotype of most cancers, but efforts to clinically target this metabolic alteration have been challenging

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Similarly to CQ, treatment with leupeptin/NH 4 Cl resulted in the downregulation of both VEGFR3 and PROX1 proteins (Supplementary Fig

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Therefore, it could be expected that the observed effect of DMSO on sulfur metabolism in these lines would not be identical