Assessment of Interleukin 15 (IL-15) Gene Polymorphism in Adult Patients with Acute Lymphoblastic Leukemia

  • Y El-Ghobashy
  • R Azmy
  • A Dawood
  • A Kelany
  • E Shaltot
  • M El-Daly

Abstract

From its beginnings two decades ago with the analysis of chromosomal translocation break points, research into the molecular pathogenesis of acute lymphoblastic leukemia (ALL) has now progressed to the large scale sequencing of candidate genes that might be linked to the pathogenesis of leukemia. Interleukon-15 (IL-15) gene has gained the interest of many oncologist with five single nucleotide polymorphisms (SNPs) proved to be associated with childhood ALL.The aim of this study was to investigate the relationship between IL-15 gene polymorphisms and the risk for adult
ALL and whether these polymorphisms are related to the immunophenotype of the disease. This study included 60 subjects classified into 2 groups: 30 patients with adult ALL (ALL group) and 30 healthy subjects of matched age and sex as control group. All subjects were genotyped for rs10519613 and rs35964658 polymorphisms of IL-15 gene using PCR-RFLP technique.Results revealed that there was no statistical difference between ALL group and control group regarding the distribution of the genotypes of both for rs10519613 and rs35964658 polymorphisms however there was 2.1 fold increased risk for ALL in C-allele carriers of rs10519613 polymorphism (OR:2.1 95% CI: 0.45 – 9.84). Concerning immunophenotype of the disease, there was no statistical difference between B-cell type and T-cell type regarding the distribution of the genotypes of the two polymorphisms, however there is 1.2 fold increased risk for B-cell type in G-allele carriers of rs35964658 polymorphism (OR:1.2 95% CI: 0.07 – 19.63).It was concluded that there was no association between both rs10519613 and rs35964658 polymorphisms and neither the risk of ALL nor the immune-phenotype of the disease.

Key wards: IL-15, cytokines, genetic polymorphism, ALL

Section
Articles

Journal Identifiers


eISSN: 1687-1502