Aberrant expression of ID2 protein and its correlation with EBV-LMP1 and P16(INK4A) in classical Hodgkin lymphoma in China

BMC Cancer. 2008 Dec 19:8:379. doi: 10.1186/1471-2407-8-379.

Abstract

Background: The relationships between the expression of ID2, EBV-LMP1 and P16(INK4A) in Chinese classical Hodgkin lymphoma are unknown and need exploring.

Methods: Samples of classical Hodgkin lymphoma from 60 Chinese patients were analyzed for the expression of ID2, EBV-LMP1 and p16(INK4A) proteins by immunohistochemistry.

Results: ID2 protein was expressed in 83.3% of this group of classical Hodgkin lymphoma, staining strongly in both cytoplasm and nucleus of the Hodgkin and Reed-Sternberg (HRS) cells. EBV-LMP1 and P16(INK4A) were overexpressed in 85.0% and 71.7% of Hodgkin lymphoma, respectively. EBV-LMP1 was noted in the cytoplasm, membrane and nucleus of HRS cells; P16(INK4A) was in the nucleus and cytoplasm. Microscopically, ID2, EBV-LMP1 and P16(INK4A) staining distinguished the HRS cells from the complex background of lymphocytes. ID2 was positively correlated with EBV-LMP1(P < 0.01), but P16(INK4A) was inversely related to EBV-LMP1 (P < 0.05).

Conclusion: It is suggested that ID2, EBV-LMP1 and P16(INK4A) could play an important role in the evolution of classical Hodgkin lymphoma, and be considered as potential adjunct markers to identify HRS cells in diagnosis.

MeSH terms

  • Cell Membrane / metabolism
  • Cell Nucleus / metabolism
  • China
  • Cyclin-Dependent Kinase Inhibitor p16 / metabolism*
  • Cytoplasm / metabolism
  • Female
  • Hodgkin Disease / metabolism*
  • Hodgkin Disease / pathology
  • Humans
  • Immunohistochemistry
  • Inhibitor of Differentiation Protein 2 / metabolism*
  • Lymphocytes / metabolism
  • Male
  • Reed-Sternberg Cells / metabolism
  • Reed-Sternberg Cells / pathology
  • Viral Matrix Proteins / metabolism*

Substances

  • Cyclin-Dependent Kinase Inhibitor p16
  • EBV-associated membrane antigen, Epstein-Barr virus
  • ID2 protein, human
  • Inhibitor of Differentiation Protein 2
  • Viral Matrix Proteins