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Genotype frequencies for polymorphisms related to chemotherapy-induced nausea and vomiting in a Japanese population

机译:基因型频率与日本人化疗引起的恶心和呕吐相关的多态性

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BackgroundGenotype frequencies for chemotherapy-induced nausea and vomiting (CINV)-related polymorphisms have not yet been reported for Japanese subjects. MethodsWe analyzed 10 genotype frequencies for following polymorphisms associated with the development of CINV: serotonin 5-HT3 receptors (HTR3); neurokinin-1 receptors (Tachykinin-1 receptors, TACR1); dopamine D2 receptors (DRD2); and catechol-O-methyltransferase (COMT). ResultsAll polymorphisms were successfully genotyped in 200 Japanese subjects and were in Hardy-Weinberg equilibrium. Almost all genotype frequencies were similar to those in the HapMap database or in the previous reports, while frequencies for the Y192H polymorphism in TACR1 were different in Japanese subjects from those in a previous report. ConclusionsThe present study revealed genotype frequencies for polymorphisms, which were related to the appearance of CINV in Japanese subjects. Individual therapy based on genotype variations for each race is needed to allow cancer patients to undergo chemotherapy more safely and to understand etiology of CINV.
机译:背景尚未有针对日本受试者的化疗引起的恶心和呕吐(CINV)相关多态性的基因型频率报道。方法我们分析了10种基因型频率,以发现与CINV发生有关的以下多态性:血清素5-HT 3 受体(HTR3);神经激肽1受体(Tachykinin-1 receptors,TACR1);多巴胺D 2 受体(DRD2);和儿茶酚-O-甲基转移酶(COMT)。结果所有多态性均在200名日本受试者中成功进行了基因分型,并处于Hardy-Weinberg平衡状态。几乎所有基因型频率都与HapMap数据库或以前的报告中的频率相似,而日本受试者中TACR1中Y192H多态性的频率与以前的报告中的频率不同。结论本研究揭示了多态性的基因型频率,其与日本受试者中CINV的出现有关。需要基于种族的基因型变异的个体疗法,以使癌症患者更安全地接受化疗并了解CINV的病因。

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