Pharmacogenomics · 2022 · 11 citations · 16 references
MedicineOncologyPharmacologyMedical GeneticsPharmacogeneticsPharmacogenomicsAnthracycline CardiotoxicityCancer PharmacogenomicsCancer Therapy-related CardiotoxicityGermline Pharmacogenetic VariationPharmacogenomics In ChildrenPharmacogenomics In Pediatric OncologyAnthracycline-induced CardiomyopathyAnthracycline-induced CardiotoxicityGenetic Risk VariantsPediatric Anthracycline CardiotoxicityPharmacogenomic ImplicationsPharmacogenomic VariationProtective Genetic VariantsRisk Gene Variants
Background: The aim of this study was to evaluate the association between well-defined genetic risk variants in SLC28A3, RARG and UGT1A6 and anthracycline-induced cardiotoxicity in Mexican pediatric patients. Methods: We tested a cohort of 79 children treated with anthracyclines for the presence of SLC28A3-rs7853758, RARG-rs2229774 and UGT1A6-rs17863783. Results: The SLC28A3-rs7853758 variant was more frequent in this cohort, while the UGT1A6-rs17863783 and RARG-rs2229774 variants were present at lower frequencies. A clinically important decrease of fractional shortening was associated with SLC28A3-rs7853758 variant. Conclusion: In this cohort, 39.2% of patients carried the protective SLC28A3 variant. A small number of tested patients have the risk variants of UGT1A6 and RARG. None of the patients shared the two risk variants.
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José Luis Zamorano, Patrizio Lancellotti, Daniel Muñoz et al. · European Heart Journal · 2016 · 2.5K citations · Full text
Medicine, Oncology, Toxicology +17
Identification of the molecular basis of doxorubicin-induced cardiotoxicity
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Medicine, Oncology, Pharmacology +17