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Germline variant determines epigenetic regulation of the anti-cancer drug metabolism gene dihydropyrimidine dehydrogenase ().胚系变异决定了抗癌药物代谢基因二氢嘧啶脱氢酶 () 的表观遗传调控。
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Incomplete DPYD haplotype B3 in a patient with locally advanced gastric cancer: Reconsidering the 5-FU dosage strategy.局部晚期胃癌患者中存在不完全DPYD单倍型B3:重新考虑5-氟尿嘧啶剂量策略。
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用于 DPYD 的参考物质的特征描述:一个 GeT-RM 合作项目。

Characterization of Reference Materials for DPYD: A GeT-RM Collaborative Project.

机构信息

Division of Clinical Pharmacology, Toxicology and Therapeutic Innovation, Children's Mercy Research Institute, Kansas City, Missouri.

RPRD Diagnostics, Milwaukee, Wisconsin; Section on Genomic Pediatrics, Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin.

出版信息

J Mol Diagn. 2024 Oct;26(10):864-875. doi: 10.1016/j.jmoldx.2024.06.004. Epub 2024 Jul 18.

DOI:10.1016/j.jmoldx.2024.06.004
PMID:39032822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11818935/
Abstract

The DPYD gene encodes dihydropyrimidine dehydrogenase (DPD), which is involved in the catalysis of uracil and thymine, as well as 5-fluorouracil (5-FU), which is used to treat solid tumors. Patients with decreased DPD activity are at risk of serious, sometimes fatal, adverse drug reactions to this important cancer drug. Pharmacogenetic testing for DPYD is increasingly provided by clinical and research laboratories; however, only a limited number of quality control and reference materials are currently available for clinical DPYD testing. To address this need, the Division of Laboratory Systems, Centers for Disease Control and Prevention-based Genetic Testing Reference Materials Coordination Program, in collaboration with members of the pharmacogenetic testing and research communities and the Coriell Institute for Medical Research, has characterized 33 DNA samples derived from Coriell cell lines for DPYD. Samples were distributed to four volunteer laboratories for genetic testing using a variety of commercially available and laboratory-developed tests. Sanger sequencing was used by one laboratory and publicly available whole-genome sequence data from the 1000 Genomes Project were used by another to inform genotype. Thirty-three distinct DPYD variants were identified among the 33 samples characterized. These publicly available and well-characterized materials can be used to support the quality assurance and quality control programs of clinical laboratories performing clinical pharmacogenetic testing.

摘要

DPYD 基因编码二氢嘧啶脱氢酶(DPD),该酶参与尿嘧啶和胸腺嘧啶的催化,以及 5-氟尿嘧啶(5-FU)的催化,后者用于治疗实体瘤。DPD 活性降低的患者使用这种重要的癌症药物时,有发生严重甚至致命的药物不良反应的风险。临床和研究实验室越来越多地提供 DPYD 的药物遗传学检测;然而,目前用于临床 DPYD 检测的质量控制和参考材料数量有限。为满足这一需求,疾病预防控制中心基于实验室系统的遗传检测参考材料协调计划司与药物遗传学检测和研究界成员以及科里尔医学研究所合作,对源自科里尔细胞系的 33 个 DPYD DNA 样本进行了特征描述。这些样本被分发给四个志愿实验室,使用各种市售和实验室开发的检测方法进行基因检测。一个实验室使用 Sanger 测序,另一个实验室使用 1000 基因组计划提供的公开全基因组序列数据来告知基因型。在 33 个被描述的样本中,鉴定出 33 种不同的 DPYD 变体。这些公开且特征明确的材料可用于支持进行临床药物遗传学检测的临床实验室的质量保证和质量控制计划。