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中国临床药理学与治疗学 ›› 2014, Vol. 19 ›› Issue (7): 818-823.

• 综述与讲座 • 上一篇    下一篇

基因多态性对巯嘌呤类药物作用影响的研究进展

谢偲, 岳丽杰   

  1. 遵义医学院,深圳市儿童医院儿科研究所,深圳 518026,广东
  • 收稿日期:2013-07-12 修回日期:2014-06-17 发布日期:2014-07-21
  • 通讯作者: 岳丽杰,女,博士,教授,硕士生导师,研究方向:儿科疾病及血液肿瘤。 Tel: 0755?83936071  E?mail: 2376028869@qq.com
  • 作者简介:谢偲,女,硕士研究生,研究方向:儿科疾病及血液肿瘤。 Tel: 0755-83936071 E-mail: xiecai_zy@163.com
  • 基金资助:
    国家自然科学基金资助项目(30471830); 深圳市科技计划重点项目(20110101)

Recent progress in research and development of the impact of gene polymorphisms on thiopurine drugs

XIE Cai, YUE Li-jie   

  1. Institute of Pediatric Research, Shenzhen Children's Hospital of Zunyi Medical College, Shenzhen 518026, Guangdong, China
  • Received:2013-07-12 Revised:2014-06-17 Published:2014-07-21

摘要: 基因多态性是影响巯嘌呤类药物在体内代谢,最终造成药物疗效和毒性差异的主要原因。近年来研究发现,单一药物代谢酶或转运体的基因多态性与巯嘌呤类药物临床不良反应不完全相关,而多基因分析可能更好地解释患者对该药的不耐受原因。本文介绍了多种与巯嘌呤类药物有关的酶基因多态性的研究情况,同时就其代谢特点及与该药敏感性的关系进行综述。

关键词: 巯嘌呤, 基因多态性, 药物代谢酶, 药物转运体

Abstract: Gene polymorphisms affect the metabolisms of thiopurine drugs, which eventually become the main reason for the differences in efficacy and toxicity. Recently some researches have showed that there were no complete correlations between a single gene polymorphism of drug metabolizing enzyme or transporter and clinical adverse reactions of thiopurine drugs. However, the reasons of drug intolerance were probably more related to multi-genetic analyses. In this article, some of the recent developments of gene polymorphisms of several enzymes about thiopurine drugs were introduced. Meanwhile, the relationships between their metabolic characteristics and drug susceptibility were reviewed.

Key words: thiopurine, gene polymorphism, drug metabolizing enzyme, drug transporter

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