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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Polymorphisms in the novel serotonin receptor subunit gene HTR3C show different risks for acute chemotherapy-induced vomiting after anthracycline chemotherapy
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Polymorphisms in the novel serotonin receptor subunit gene HTR3C show different risks for acute chemotherapy-induced vomiting after anthracycline chemotherapy

机译:新型5-羟色胺受体亚基基因HTR3C的多态性显示蒽环类药物化疗后急性化疗引起的呕吐的不同风险

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摘要

The aim of this study was to correlate chemotherapy-induced nausea and vomiting (CINV) with commonly occurring single nucleotide polymorphisms (SNP) in the 5-hydroxytryptamine receptor 3 genes (HTR3). Women with breast cancer without previous chemotherapy were eligible for this prospective study. All patients received epirubicin, with or without cyclophosphamide, and preventive medication with ondansetron and dexamethasone. The patients documented every vomiting event on an hourly basis. Real-time polymerase chain reaction (PCR) analysis was performed for the following nonsynonymous SNPs: p.Y129S (HTR3B), p.K163N (HTR3C) and p.A405G (HTR3C). The overall proportion of patients (total n = 110) who reported vomiting in the first 24 h after chemotherapy was 31.8%. The variant genotype of K163N (HTR3C) was associated with vomiting, which occurred in 50.0% (P = 0.009). Polymorphisms in the HTR3C gene could serve as a predictive factor for CINV in patients undergoing moderately emetogenic chemotherapy.
机译:这项研究的目的是将化疗引起的恶心和呕吐(CINV)与5-羟色胺3基因(HTR3)中常见的单核苷酸多态性(SNP)相关联。既往未接受过化疗的乳腺癌女性有资格参加这项前瞻性研究。所有患者均接受表柔比星(含或不含环磷酰胺)以及恩丹西酮和地塞米松的预防药物治疗。患者每小时记录一次每次呕吐事件。对以下非同义SNP进行实时聚合酶链反应(PCR)分析:p.Y129S(HTR3B),p.K163N(HTR3C)和p.A405G(HTR3C)。在化疗后的最初24小时内报告呕吐的患者总数(总n = 110)为31.8%。 K163N(HTR3C)的变异基因型与呕吐相关,发生率为50.0%(P = 0.009)。 HTR3C基因的多态性可以作为中度致癌化疗患者CINV的预测因素。

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