Epstein-Barr virus infection is inversely correlated with the expression of retinoblastoma protein in Reed-Sternberg cells in classic Hodgkin lymphoma

Int J Clin Exp Pathol. 2014 Oct 15;7(11):7508-17. eCollection 2014.

Abstract

Classic Hodgkin lymphoma (cHL) is characterized by few neoplastic Hodgkin/Reed-Sternberg (H/RS) cells in a background of intense inflammatory infiltrate. Epstein-Barr virus (EBV) has been shown to affect cell cycle and regulation of apoptosis. In total, 82 cases of cHL were studied. Five- micrometer sections were prepared and stained with haematoxylin and eosin and immunohistochemical streptavidin-biotin methods for EBV-LMP-1, pRb, ki-67 and cleaved caspase-3. In-situ hybridization for EBV encoded RNA was used to confirm the detection of EBV in H/RS cells. There were 45 nodular sclerosis, 28 mixed cellularity, 4 lymphocyte-rich, and 5 lymphocyte depletion subtypes in this series of cases. EBV and pRb were detected in 55% (46/82) and 64% (50/82) of the cases respectively. EBV was detected in 78% (25/32) of pRb-negative cases and 81% (29/36) of EBV-negative cases are pRb-positive. A statistically significant inverse relationship was observed between the presence of EBV and expression of pRb (P = 0.001). In conclusion, EBV infection is inversely correlated with pRb in H/RS cells in cHL.

Keywords: Epstein Barr virus; Hodgkin lymphoma; pRb.

MeSH terms

  • Apoptosis
  • Caspase 3 / metabolism
  • Cell Cycle
  • Cell Division
  • Cell Proliferation
  • Epstein-Barr Virus Infections / metabolism*
  • Epstein-Barr Virus Infections / pathology
  • Epstein-Barr Virus Infections / virology
  • Herpesvirus 4, Human / genetics
  • Herpesvirus 4, Human / isolation & purification*
  • Hodgkin Disease / metabolism*
  • Hodgkin Disease / pathology
  • Hodgkin Disease / virology
  • Humans
  • In Situ Hybridization
  • Ki-67 Antigen / metabolism
  • Lymphocytes / pathology
  • RNA, Viral / genetics
  • Reed-Sternberg Cells / metabolism*
  • Reed-Sternberg Cells / pathology
  • Reed-Sternberg Cells / virology
  • Retinoblastoma Protein / metabolism*

Substances

  • Ki-67 Antigen
  • RNA, Viral
  • Retinoblastoma Protein
  • Caspase 3