The low frequency of defective TPMT alleles in Turkish population: a study on pediatric patients with acute lymphoblastic leukemia.

Yazan: admin Tarih: AÄŸu 3rd, 2008 | Kategori:: Leukemia(Kan Kanseri)

Am J Hematol. 2007 Oct;82(10):906-10.

Biochemistry Graduate Programme and Department of Biological Sciences, Middle East Technical University, 06531 Ankara, Turkey.

6- (6MP) is an essential used in the treatment of (ALL). Thiopurine methyltransferase (TPMT) polymorphisms are the major determinants of interindividual differences in the severe toxicity or efficacy of 6MP. Four variant alleles, TPMT*2, TPMT*3A, TPMT*3B, and TPMT*3C, are responsible over the 80% of low or undetectable . The frequencies of these variants were investigated among 106 children with ALL in . TPMT*3A and TPMT*3C were the only deficiency alleles detected in with an of 0.9% for both. While *3C in was found to be very similar to Asian and other , *3A was significantly (P < 0.05) lower. So far, studies showed that the of other drug metabolizing enzymes like CYP2E1, CYP1A1, GSTM1/ T1 in were similar to . However, we found that the distribution of TPMT polymorphisms in was significantly lower than those in other Caucasians like British, French, and Italian whereas the distributions of TPMT variants were found to be very similar to Kazak population which is also Caucasian in ethnic origin. In this study, the clinical histories of the patients in the sample population were also examined, retrospectively. The patients with heterozygous or homozygous mutant genotypes had developed severe neutropenia and infection during 6MP therapy. The study provides the first data on the frequency of common TPMT variants in the , based on analysis of with ALL.



Yorum Yapin

Yorum yapabilmek icin giris yapmalisiniz.