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Association between methylenetetrahydrofolate reductase polymorphism C677T and risk of chronic myeloid leukemia in Serbian population
18
Citations
16
References
2011
Year
Mixed-phenotype Acute LeukemiaGeneticsGenetic EpidemiologyHuman PolymorphismPathologySerbian PopulationEpigeneticsClinical GeneticsMyeloid NeoplasiaHematological MalignancyHematologyMthfr 677Public HealthMolecular DiagnosticsCancer ResearchVariant InterpretationMethylenetetrahydrofolate ReductaseStatistical GeneticsEpidemiologyChronic Myeloid LeukemiaCancer RiskMedicine
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.
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