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[126] investigated if they share similar substrates, and through an assay involving a radiolabeled hydrophobic PMEA precursor, they discovered that MRP5 serves as an active transporter of the drug

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The combination might therefore synergistically relieve Epstein-Barr virus-mediated repression by promoting both transcriptional activation (via vitamin D receptor-tumour protein p53 interaction) and post-translational stabilisation of tumour protein p53 (via curcumin-induced stress response), ultimately restoring downstream p21 expression and cell-cycle arrest