应将DPYD基因型扩展到罕见变异:报告了两例表型/基因型不一致的病例
Paul Vilquin1,2, Yves Medard1, Fabienne Thomas3,4
1Service de Génomique des Tumeurs et Pharmacologie, Hôpital Saint-Louis, Assistance Publique Hôpitaux de Paris, Paris, France.
Cancer chemotherapy and pharmacology
|January 2, 2025
概括
二皮里米丁脱酶 (DPD) 缺乏可能导致皮里米丁药物致死性毒性. 将DPD表型与全基因测序配对可以提高准确性,特别是对于罕见的变异,确保更安全的癌症治疗.
科学领域:
- 药物基因组学 药物基因组学
- 在瘤学瘤学.
- 临床化学 临床化学
背景情况:
- 二皮里米丁脱酶 (DPD) 对于代谢-5-甲 (5FU) 和capecitabine等皮里米丁至关重要.
- 由DPYD基因变异引起的DPD缺乏症可能导致癌症患者接受标准剂量的严重毒性.
- 目前的查涉及DPYD通过血 uracil ([U]) 和dihydrouracil ([UH2]) 水平的基因型和表型.
关键词:
(310):二皮里米丁脱酶.基因测序的基因测序基因型 基因型 基因型药物原生药物制造的方法现象型 现象型 是一种现象型.罕见的变种 罕见的变种乌拉西尔 (Uracil) 是一个叫做乌拉西尔的词.更多相关视频
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