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Gene mutation of thiopurine S-methyltransferase in Uygur Chinese

  • Pharmacogenetics
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Abstract

Objective

This study was to investigate the gene mutation of thiopurine S-methyltransferase (TPMT) in Uygur Chinese.

Methods

Polymerase chain reaction-based methods were used to analyze three commonly reported inactivating mutations—G238C, G460A and A719G.

Results

One TPMT*3A heterozygote and five TPMT*3C heterozygotes were found in 160 Uygur Chinese subjects, and allele frequencies of TPMT*3A and TPMT*3C were 0.3% and 1.6%, respectively.

Conclusion

TPMT*3C is a common mutant allele in Uygur Chinese, while TPMT*3A is a rare mutant allele in Uygur Chinese.

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References

  1. McLeod HL, Krynetski EY, Relling MV, Evans WE (2000) Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia. Leukemia 14:567–572

    CAS  PubMed  Google Scholar 

  2. Weinshilboum R (2001) Thiopurine pharmacogenetics: clinical and molecular studies of Thiopurine methyltransferase. Drug Metab Dispos 29:601–605

    CAS  PubMed  Google Scholar 

  3. Yates CR, Krynetski EY, Loennechen T, Fessing MY, Tai HL, Pui CH, et al (1997) Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathiopurine and mercaptopurine intolerance. Ann Intern Med 126:608–614

    CAS  PubMed  Google Scholar 

  4. Hon YY, Fessing MY, Pui CH, Relling MV, Krynetski EY, Evans WE (1999) Polymorphism of the thiopurine S-methyltransferase gene in African-Americans. Hum Mol Genet 8:371–376

    Article  CAS  PubMed  Google Scholar 

  5. McLeod HL, Pritchard SC, Githang’a J, Indalo A, Ameyaw MM, Powrie RH, et al (1999) Ethnic differences in thiopurine methyltransferase pharmacogenetics: evidence for allele specificity in Caucasian and Kenyan individuals. Pharmacogenetics 9:773–776

    CAS  PubMed  Google Scholar 

  6. Collie-Duguid ES, Pritchard SC, Powrie RH, Sludden J, Collier DA, Li T, Mcleod HL (1999) The frequency and distribution of thiopurine methyltransferase alleles in Caucasian and Asian populations. Pharmacogenetics 9:37–42

    CAS  PubMed  Google Scholar 

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Acknowledgements

The authors thank Dr. Weinshilboum (Mayo Medical School, Mayo Clinic, Rochester, USA) for providing DNA reference samples. This work was supported by the National Nature Science Fund of China (No. 30171098). The experiments comply with the current law of the People’s Republic of China.

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Correspondence to Min Huang.

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Zhang, JP., Guan, YY., Xu, AL. et al. Gene mutation of thiopurine S-methyltransferase in Uygur Chinese. Eur J Clin Pharmacol 60, 1–3 (2004). https://doi.org/10.1007/s00228-004-0730-7

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  • DOI: https://doi.org/10.1007/s00228-004-0730-7

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