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A functional polymorphism in the miR-146a gene is associated with the risk of childhood acute lymphoblastic leukemia: a preliminary report

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Tumor Biology

Abstract

Growing evidence showed that microRNAs (miRs) are involved in normal hematopoiesis and the pathogenesis of several hematological malignancies. Genetic variations or mutations occurring in the miR gene region may affect the property of miRs through altering miR expression and/or maturation. The aim of the present study was to evaluate the possible relationship between two miRs polymorphisms, hsa-miR-146a (rs2910164 G>C) and hsa-miR-499 (rs3746444 T>C), and the susceptibility to childhood acute lymphoblastic leukemia (ALL) in a sample of Iranian population. This case–control study was performed on 75 children diagnosed with ALL and 115 age- and sex-matched children with no history of cancer of any type (as the control group). Tetra-primer amplification refractory mutation system-polymerase chain reaction was applied for genotyping the variants. We found that the rs2910164 G>C variant of hsa-miR-146a significantly increased the risk of ALL (CC vs. GG, OR = 4.24, 95 %CI = 1.52–11.87, P = 0.006; GC vs. GG, OR = 3.55, 95 % CI = 1.41–8.93, P = 0.007; C vs. T, OR = 1.73, 95 % CI = 1.13–2.67, P = 0.012). With respect to hsa-miR-499 rs3746444 T/C, no significant difference in allele and genotype frequencies of the rs3746444 variant between ALL patients and controls was observed. Our results for the first time demonstrated that the miR-146a rs2910164, but not miR-499 rs3746444 variant, was associated with increased risk for developing pediatrics ALL in an Iranian population.

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Acknowledgment

This paper was based on M.Sc. thesis of SH, and the deputy for Research at Zahedan University of Medical Sciences provided the fund.

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Correspondence to Mohammad Hashemi.

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Hasani, SS., Hashemi, M., Eskandari-Nasab, E. et al. A functional polymorphism in the miR-146a gene is associated with the risk of childhood acute lymphoblastic leukemia: a preliminary report. Tumor Biol. 35, 219–225 (2014). https://doi.org/10.1007/s13277-013-1027-1

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  • DOI: https://doi.org/10.1007/s13277-013-1027-1

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