Association between methylenetetrahydrofolate reductase polymorphism C677T and risk of chronic myeloid leukemia in Serbian population

被引:20
|
作者
Jakovljevic, Ksenija [1 ]
Malisic, Emina [1 ]
Cavic, Milena [1 ]
Radulovic, Sinisa [1 ]
Jankovic, Radmila [1 ]
机构
[1] Inst Oncol & Radiol Serbia, Dept Expt Oncol, Belgrade 11000, Serbia
关键词
MTHFR polymorphisms; genotyping; CML; ACUTE LYMPHOBLASTIC-LEUKEMIA; MTHFR; GENE; SUSCEPTIBILITY; GENOTYPE; MUTATION; DISEASE; CANCER; DNA;
D O I
10.3109/10428194.2011.645210
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Methylenetetrahydrofolate reductase (MTHFR) is a key enzyme regulating the intracellular folate metabolism which plays an important role in carcinogenesis through DNA methylation and nucleotide synthesis. The common MTHFR single nucleotide polymorphism C677T has been reported to be associated with reduced enzymatic activity. In order to investigate the influence of this polymorphism on the risk of chronic myeloid leukemia (CML), we performed a case-control study in a Serbian population of 52 patients with CML and 53 healthy control subjects. MTHFR C677T polymorphism genotyping was assessed using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. The results demonstrated no statistical difference in MTHFR 677 frequency distribution between patient and control groups. Our findings suggest that MTHFR 677 gene variants have no significant influence on the susceptibility to CML in a Serbian population.
引用
收藏
页码:1327 / 1330
页数:4
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