期刊文献+

巯嘌呤甲基转移酶遗传多态性的研究进展

下载PDF
导出
摘要 临床上巯嘌呤类药物应用广泛,但此类药物的血液毒性、肝脏毒性、胰腺炎等不良反应的发生率较高。研究发现,巯嘌呤甲基转移酶(TPMT)的遗传多态性与巯嘌呤类药物不良反应的发生密切相关。在使用巯嘌呤类药物之前对患者进行酶活性测定及基因型分析,可为指导临床个体化、安全用药提供依据。
出处 《中国麻风皮肤病杂志》 2011年第8期561-563,共3页 China Journal of Leprosy and Skin Diseases
  • 相关文献

参考文献17

  • 1Corominas H, Baiget M. Clinical utility of thiopurine S - methyl- ransferase genotyping J. Am J Pharnacogenomics 2004 ;4( 1 ) : 1 - 8.
  • 2Stanulia M, Schaeffeler E, Flohr T, et al. Thiopurine methyltransferase (TPMT) genotype and early treatment response to mercap topurine in childhood acute lymphoblastic leukemia. JAMA 2005;293 (12) : 1485 - 1489.
  • 3Zhang JP, Zhou SF, Chen X, et al. Determination of intra - ethnic difference in the polymorphisms of thiopurine S - methyltransferase in Chinese. Clin Chim Acta 2006; 365 ( 1/2 ) : 337 - 341.
  • 4Schaeffeler E, Stanulla M, Greil J, et al. A novel TPMT missense mutation associated with TPMT deficiency in a 5 - year - old boy with ALL. Leukemia 2003;17(7):1422- 1424.
  • 5tajia- Chayeb L, Vidal- Millan S, Gutierrez O, et al. Thiopurine S- methyltransferase gene (TMFF) polymorphisms in a Mexican population of healthy individuals and leukemic patients. Med Oncol 2008;25(1) :56 - 62.
  • 6Kihiro T, Mayumi S, Saorik K, et al. Thiopurine S- methyltransferase gene polymorphism in Japanese patients with autoimmune liver diseases. Liver Int 2007;27(1) :95 - 100.
  • 7Hakooz N, Amfat T. Genetic analysis of thiopurine methyltransferase polymorphism in the Jordanian population. Eur J Clin Pharmacol 2010;66:999 - 1003.
  • 8Lu HF, Shi MC, Chang YS, et al. Molecular analysis of thiopurine Smethyltransferase alleles in China Taiwan aborigines and Taiwan Residents. J Clin Pharm Ther 2006;31(1) :93 - 98.
  • 9魏红,黄民,李智毅,张祯,张建萍,吴珏珩.中国哈萨克族人硫嘌呤甲基转移酶活性分布和基因多态性[J].中国临床药理学杂志,2005,21(6):423-426. 被引量:8
  • 10张建萍,黄民,关永源,白丽,魏红,吴珏珩.中国新疆维吾尔族硫嘌呤甲基转移酶基因突变研究[J].中国临床药理学杂志,2003,19(5):345-347. 被引量:4

二级参考文献35

  • 1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.
  • 2Zhang JP, Huang M, Guan YY, et al. Molecular mechanisms of genetic polymorphim of thiopurine S-methyltransferase. Chin J Clin Pharmacol, 2002, 18 , 453-457.
  • 3Yates CR, Krynetski EY, Loennechen T, et al. Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basts for azathiopurine and mercaptopurine intolerance. Ann Intern Med, 1997, 126: 608-614.
  • 4Tai 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.
  • 5Collie-Duguid ES, Pritchard SC, Powrie RH, et al. The frequency and distribution of thiopurine methyltransferase alleles in Caucasian and Asian populations. Pharmacogenetics, 1999,9: 37-42.
  • 6Weinshilboum R. Thiopurine pharmacogenetics: clinical and molecular studies of thiopurine methyltransferase. Drug Metab Dispos, 2001, 29: 601-605.
  • 7Spire-Vayron de la Moureyre C, Debuysere H, Sabbagh N, et al.Detection of known and new mutations in the thiopurine S-methyltransferase gene by single-strand conformation polymorphism analysis. Hum Murat, 1998, 12, 177-185.
  • 8Colombel JF, Ferrari N, Debuysere H, et al. Genotypic analysis of thiopurine S-methyltransferase in patients with Crohn's disease and severe myelosuppression during azathiopurine therapy.Gastroenterology, 2000, 118: 1025-1030.
  • 9Otterness D, Szumlanski C, Lennard L, et al. Human thiopurine methyltransferase pharmacogenetics : gene sequence polymorphisms. Clin Pharmacol Ther, 1997, 62: 60-73.
  • 10Krynetski EY, Tai HL, Yates CR, ,t al. Genetic polymorphism of thiopurine S-methyhransferase, clinical importance and molecular mechanisms. Pharmacogenetics, 1996, 6: 279-290.

共引文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部