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硫嘌呤甲基转移酶分子机制研究进展 被引量:2

Molecular Mechanisms of Genetic Polymorphism of Thiopurine S-Methyltransferase (TPMT)
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摘要 硫嘌呤甲基转移酶(TPMT)在硫嘌呤类药物的体内代谢中起着关键作用,其活性水平与药物效应及毒副作用密切相关。TPMT活性具有遗传多态性和种族差异。TPMT酶活性降低或缺乏与其基因突变密切相关。对TPMT遗传多态性分子基础的研究具有重要意义。本文综述有关TPMT基因表达调控和TPMT基因突变的分子机制的研究进展。 Thiopurine s-methyltransferase (TPMT) plays an important role in the metabolism of thiopurines. Phenotypic polymorphism of TPMT in different populations have been widely studied. TPMT genotype correlates well with in vivo enzyme activity in erythrocytes and is closely associated with risk of toxicity. Genetic mutations are responsible for TPMT deficiency. It is very important to study the molecular basis for altered TPMT activity. This article reviews the genomic structure and genetic mutation of TPMT.
出处 《中国临床药理学杂志》 CAS CSCD 北大核心 2002年第6期448-451,474,共5页 The Chinese Journal of Clinical Pharmacology
关键词 硫嘌呤甲基转移酶 分子机制 研究进展 基因结构 基因突变 thiopurine S-methyltransferase (TPMT), genomic structure, genetic mutation
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  • 1Krynetski EY, Evans WE. Pharmacogenetics as a Molecular basis for individualized drug therapy: the thiopurine S-methyltransferase paradigm. Pharmaceut Res, 1999; 16: 342~349.
  • 2Weinshilboum RM, Sladek SL. Mercaptopurine pharmacogenetics:monogenic inheritance of erythrocyte thiopurine methyltransferase activity. Am J Hum Genet, 1980; 32: 651~662.
  • 3吴珏珩,张建萍,姜文奇,黄民.硫嘌呤甲基转移酶多态性的研究进展及其临床意义[J].癌症,2001,20(12):1439-1441. 被引量:6
  • 4Honchel R; Aksoy IA; Szumlanski C, et al. Human thiopurine methyltransferase: molecular cloning and expression of T84 colon carcinoma cell cDNA. Mol Pharmacol, 1993; 43: 878~887.
  • 5Lee D, Szumlanski C, Houtman J, et al. Thiopurine transferase pharmacogenetics. Cloning of Human liver cDNA and a processed pseudogene on human chromosome t 8q21.1. Drug Met Disp, 1995;23: 398~405.
  • 6Szumlanski C, Otterness D, Her C, et al. Thiopurine methyltransferase pharmacogenetics: human gene cloning and characterization of a common polymorphism. DNA Cell Biol, 1996;15:17~30.
  • 7Krynetski EY, Fessing MY, Yates CR, et al. Promoter and intronic sequences of the human thiopurine S-methyltransferase (TPMT)gene isolated from a human Pacl genomic library. Pharmaceut Res, 1997; 14: 1672~1678.
  • 8Krynetski EY, Evans WE. Genetic polymorphism of thiopurine Smethyltransferase: molecular mechanisms and clinical importance.Pharmacology, 2000; 61: 136~146.
  • 9Fessing MY, Krynetski EY, Zambetti GP, et al. Functional characterization of the human thiopurine S-methyltransferase (TPMT) gene promoter. Eur J Biochem, 1998; 256: 510~517.
  • 10Spire-Vayron de la Moureyre C, Debuysere H, Mastain B, et al.Genotypic analysis of the polymorphic thiopurine Smethyltransferase gene (TPMT) European population. B J Pharmacol. 1998: 125:879~887

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共引文献5

同被引文献18

  • 1姜丽萍.肾移植术后服用硫唑嘌呤致粒细胞锐减3例[J].护理学杂志(综合版),1996,11(1):49-50. 被引量:2
  • 2杨志玉.硫唑嘌呤致白细胞下降死亡1例[J].中国皮肤性病学杂志,1996,10(15):314-314.
  • 3张建萍 黄民 关永源 等.广东瑶族和汉族儿童TPMT遗传多态性研究[J].中国临床药理学杂志,2002,18:418-421.
  • 4Weinshilboum R. Thiopurine pharmacogenetics: clinical and molecular studies of thiopurine methyltransferase[J]. Drug Met Disp, 2001; 69: 601-605.
  • 5Krynetski EY, Evans WE. Genetic polymorphism of thiopurine S-methyltransferase: molecular mechanisms and clinical importance[J]. Pharmacology, 2000; 61: 136-146.
  • 6Mcleod HL, Krynetski EY, Relling MV, et al. Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia[J]. Leukemia, 2000; 14: 567-572.
  • 7Yates CR, Krynetski EY, Ferreira F, et al. Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathiopurine and mercaptopurine intolerance[J]. Ann Intern Med, 1997; 126: 608-614.
  • 8KumagaiK, Hiyama K, Ishioka S, et al. Allelotype frequency of the thiopurine methyltransferase (TPMT) gene in Japanese[J]. Pharmacogenetic, 2001; 11: 275-278.
  • 9Tai HL, Fessing MY, Bonten EJ, et al. Enhanced proteasomal degradation of mutant human thiopurine S-methyltransferase (TPMT) in mammalian cells: Mechanism for TPMT protein deficiency inherited by TPMT*2, TPMT*3A, TPMT*3B or TPMT*3C. Pharmacogenetics, 1999; 9: 641-650.
  • 10穆荣.硫唑嘌呤.见:蒋明,林孝义,朱立平,等,主编.中华风湿病学.北京:华夏出版社,2004.1730.

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