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Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia.

Angela Gutierrez-CaminoChantal RicherPascal St-OngeElixabet Lopez-LopezAna Carbone BañeresNagore Garcia de AndoinAna SastreItziar AstigarragaIdoia Martin-GuerreroDaniel SinnettAfrica Garcia-Orad
Published in: Epigenomics (2020)
Aim: To determine the role of single nucleotide polymorphisms (SNPs) in noncoding RNAs in childhood acute lymphoblastic leukemia (ALL) subtypes. Materials & methods: We screened all SNPs in 130 pre-miRNA genes to assess their role in the susceptibility of the most common subtypes of ALL: hyperdiploid and ETV6-RUNX1. Results: In two independent cohorts, we found a significant association between rs10406069 in miR-5196 and the risk of developing hyperdiploid ALL. This observation could be explained by the impact of the SNP on miR-5196 expression and in turn, in its target genes. Indeed, rs10406069 was associated with expression changes in SMC1A, a gene involved in sister chromatin cohesion. Conclusion: rs10406069 in miR-5196 may have a relevant role in hyperdiploid ALL risk.
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