The influence of DNMT3A and DNMT3B gene polymorphisms on acute myeloid leukemia risk in a Moroccan population.

Abstract Acute myeloid leukemia (AML) is a very complex disease that is linked to environmental, genetic and epigenetic factors. Several Studies have found that aberrations in DNA methylation process play a crucial role in leukemogenesis. The aim of this case control study was to evaluate the association between rs1569686, rs2424913 polymorphisms located in DNMT3B gene and rs7590760 polymorphism located in DNMT3A gene and AML risk in a Moroccan population. Materials and methods The present study was conducted in 142 cases of AML and 179 control subjects from the Moroccan population. Genomic DNA was isolated from whole blood samples by salting-out method and the genotype of the three polymorphisms was determined by the PCR-RFLP technique. Results The study results indicated that rs1569686 polymorphism was significantly associated with the risk of AML in dominant model (OR = 1.72, 95 % CI 1.01–2.95, P = 0.04), but not in recessive model. In stratified analysis by gender, statistically significant association between the rs2424913 CT genotype and AML was found among males (OR = 2.05, 95 % CI 1.00–4.19, P = 0.04). Similarly, the rs1569686 TT genotype was associated with an increase risk of AML (OR = 3.21, 95 % CI 1.15–8. 98, P = 0.02), this association was also found under dominant genetic model (OR = 2.47, 95 % CI 1.07–5. 67, P = 0.03) among males. However, the rs2424913 polymorphism was not associated with AML. Conclusion Our findings have shown that rs1569686 polymorphism might be a risk factor of AML in males. While, the rs2424913 polymorphism was not associated with AML. Further studies with a large sample size are needed to validate our results.