Investigation of miR9-1, miR9-2 and miR9-3 Methylation in Hodgkin Lymphoma

Pathobiology. 2015;82(5):195-202. doi: 10.1159/000432402. Epub 2015 Aug 25.

Abstract

Background: miR9 is an important tumor suppressor microRNA regulated by DNA methylation in various types of cancers.

Methods: We analyzed the methylation status of the 3 members of the miR9 family in 58 cases of Hodgkin lymphoma (HL) in comparison to 15 reactive lymph nodes. We also assessed the relationships between miR9 methylation and Epstein-Barr virus (EBV) infection and several clinicopathological parameters.

Results: We found that 84.5% of HL cases had a methylation in at least 1 of the 3 loci of miR9, whereas none of the nontumoral samples was methylated. The highest rate of methylation was found in miR9-2 (5q14.3) in 74.1% of the HL cases, followed by miR9-3 (15q26.1) in 56.9% and miR9-1 (1q22) in only 8.6% (p < 0.001). The promoter methylation of miR9-3 was more frequent in patients older than 15 years than in children (p = 0.02) and among women rather than men (p = 0.02). However, no significant correlation was found between miR9 methylation and EBV infection.

Conclusion: These results indicate that miR9 methylation, especially miR9-2, is a frequent event in HL and may be involved in HL pathogenesis, irrespective of EBV infection.

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Aged
  • Aged, 80 and over
  • Child
  • Child, Preschool
  • DNA Methylation*
  • Epstein-Barr Virus Infections / complications
  • Epstein-Barr Virus Infections / genetics
  • Epstein-Barr Virus Infections / virology
  • Female
  • Hodgkin Disease / genetics*
  • Hodgkin Disease / pathology
  • Hodgkin Disease / virology
  • Humans
  • Male
  • MicroRNAs / genetics*
  • Middle Aged
  • Promoter Regions, Genetic
  • Sex Factors
  • Young Adult

Substances

  • MicroRNAs