Results 11 to 20 of about 4,744 (194)
Implementation of DPYD testing in Bulgarian patients with cancer
Precision medicine has revolutionized cancer treatment, tailoring interventions based on individual genetic variations. Dihydropyrimidine dehydrogenase gene (DPYD) testing plays a crucial role in predicting severe fluoropyrimidine-related toxicities ...
Nelly Miteva-Marcheva +4 more
doaj +3 more sources
Translating DPYD Genotype into DPD Phenotype: Using the DPYD Gene Activity Score [PDF]
The dihydropyrimidine dehydrogenase enzyme (DPD, encoded by the gene DPYD) plays a key role in the metabolism of fluoropyrimidines. DPD deficiency occurs in 4-5% of the population and is associated with severe fluoropyrimidine-related toxicity. Several SNPs in DPYD have been described that lead to absent or reduced enzyme activity, including DPYD*2A ...
Henricks, L.M. +7 more
openaire +8 more sources
DPYD Genotyping of Patients with Fluoropyrimidine Treatment: Results of Protocol Implementation and Outcomes of Patients Carrying Unusual DPYD Variants. [PDF]
Background/Objectives: The DPYD gene encodes the enzyme dihydropyrimidine dehydrogenase that metabolizes fluoropyrimidines. Genetic variants in DPYD have been associated with altered enzyme activity; therefore, accurate detection and interpretation is critical for individualized fluoropyrimidine therapy.
Salgado Garrido J +7 more
europepmc +4 more sources
Frequent intragenic rearrangements of DPYD in colorectal tumours [PDF]
Dihydropyrimidine dehydrogenase is a crucial enzyme for the degradation of 5-fluorouracil (5FU). DPYD, which encodes dihydropyrimidine dehydrogenase, is prone to acquire genomic rearrangements because of the presence of an intragenic fragile site FRA1E.
van Kuilenburg, A +18 more
openaire +5 more sources
Introduction: Dihydropyrimidine dehydrogenase (DPD), encoded by DPYD gene, is the rate-limiting enzyme responsible for fluoropyrimidine (FP) catabolism.
Georgia Ragia +17 more
doaj +2 more sources
Nomenclature for human DPYD alleles
To standardize DPYD allele nomenclature and to conform with international human gene nomenclature guidelines, an alternative to the current arbitrary system is described. Based on recommendations for human genome nomenclature, we propose that each distinct allele be designed by DPYD followed by an asterisk and an Arabic numeral.
McLeod, H. L. +10 more
openaire +4 more sources
Background: 5-FU-based chemoradiotherapy (CRT) could be associated with severe treatment-related toxicities in patients harboring at-risk DPYD polymorphisms.
Antoine Desilets +12 more
doaj +2 more sources
Germline DPYD Variant Effect on Fluorouracil Toxicity [PDF]
The fluoropyrimidines, 5-fluorouracil (5-FU) and capecitabine, are widely used for solid tumor treatment. They can cause early-onset, severe toxicities such as neutropenia, mucositis, colitis, emesis, and hand-foot syndrome. 5-FU and capecitabine are metabolized by the DPD enzyme, coded for by the DPYD gene.
Mills, Sarah
openaire +2 more sources
Pharmacogenomics: DPYD and Prevention of Toxicity
In 2020, the introduction of pre-emptive DPYD genotyping prior to the administration of systemic fluoropyrimidine-based chemotherapy represented one of the first widespread pharmacogenetic testing programmes to be applied nationally in the United Kingdom.
J. Keen +3 more
openaire +3 more sources
Balance of care activity after EMA recommendation for DPYD gene testing in Galicia [PDF]
IntroductionSince April 2020, pretherapeutic screening for accessing the deficiency of the DPD enzyme by genotyping the dihydropyrimidine dehydrogenase gene (DPYD) is required by the European Medicine Agency (EMA) prior to the administration of ...
Almudena Gil-Rodríguez +15 more
doaj +2 more sources

