Pharmacogenomics · 2017 · 22 citations · 11 references
MedicineOncologyPharmacologyPharmacogeneticsPharmacogenomicsPharmacogenomics In OncologyCancer PharmacogenomicsCytochrome P450 InteractionsDrug DispositionHormonal Cancer TherapyHormonal TherapyOncology PharmacologyCyp2a6 MetabolismCyp2d6 Drug MetabolismCyp2d6 GenotypeCyp2d6 GenotypingCyp2d6 PharmacogeneticsCyp2d6 PhenotypingCytochrome P450 2D6Enhancer Variants
AIM: CYP2D6*2 is considered fully active, but it has been suggested that it only happens in the presence of rs5758550. This study aims to elucidate the impact of this enhancer. MATERIALS & METHODS: DNA and blood samples from women enrolled in the CYPTAM study (NTR1509) were analyzed. Fourteen CYP2D6*2 carriers without the enhancer were reclassified. The relationship of CYP2D6 phenotypes and drug levels was studied. RESULTS: : 0.290 vs 0.279). No difference was observed in mean concentrations between CYP2D6*2 individuals with and without the enhancer. CONCLUSION: The rs5758550 enhancer does not lead to improved prediction of endoxifen levels in breast cancer patients.
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Primary breast cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
Elżbieta Senkus, S. Kyriakides, Shinji Ohno et al. · Annals of Oncology · 2015 · 1.6K citations · Full text
Polymorphism of Human Cytochrome P450 2D6 and Its Clinical Significance
Shufeng Zhou · Clinical Pharmacokinetics · 2009 · 759 citations
Medicine, Genetics, Pharmacology +14
Zeruesenay Desta, Bryan A. Ward, Nadia Soukhova et al. · Journal of Pharmacology and Experimental Therapeutics · 2004 · 645 citations
Medicine, Biochemistry, Pharmacology +17