Association of DDX58 177 C > T polymorphism with decreased risk of Epstein-Barr virus-related nodular sclerosis classical Hodgkin lymphoma

Leuk Lymphoma. 2017 Feb;58(2):438-444. doi: 10.1080/10428194.2016.1190972. Epub 2016 Jun 7.

Abstract

Classical Hodgkin lymphoma (cHL) is frequently related to Epstein-Barr virus (EBV) infection. Its malignant capacity is attributed to disruption of an EBV-host balance influenced by environmental and genetic drivers. EBV structures activate Type I interferon (IFN) pathway of the innate immunity, therefore, genetic polymorphisms could influence this response. We explored the impact of four single nucleotide polymorphisms (SNPs) on EBV-associated cHL susceptibility. Toll-like receptors 9 (TLR9_rs5743836), and 3 (TLR3_rs3775291), Interleukin-28B (IL28B_rs12979860), and DEAD-box polypeptide 58 (DDX58_rs10813831) were genotyped in 73 EBV-positive and 106 EBV-negative cHL patients and 396 controls. Only DDX58_rs10813831 T-allele was decreased among EBV-positive cHL compared to controls. A stratified analysis in EBV-positive cHL showed that the reduced rate was associated with younger age and nodular sclerosis. In conclusion, DDX58_rs10813831 T-allele may be associated with a reduced risk of nodular sclerosis EBV-related cHL, which suggests a role for RIG-I (retinoic acid-inducible gene I), encoded by DDX58, in these cases.

Keywords: Classical Hodgkin lymphoma; DDX58; EBV; IFN pathway; IL28B; TLR-3; TLR-9; genetic susceptibility; single nucleotide polymorphisms.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Alleles*
  • Case-Control Studies
  • Cell Transformation, Viral
  • DEAD Box Protein 58 / genetics*
  • DEAD Box Protein 58 / metabolism
  • Epstein-Barr Virus Infections / complications*
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genotype
  • Herpesvirus 4, Human*
  • Hodgkin Disease / etiology*
  • Hodgkin Disease / metabolism
  • Hodgkin Disease / pathology*
  • Humans
  • Male
  • Middle Aged
  • Odds Ratio
  • Polymorphism, Single Nucleotide*
  • Receptors, Immunologic
  • Sclerosis
  • Young Adult

Substances

  • Receptors, Immunologic
  • RIGI protein, human
  • DEAD Box Protein 58