The copy number of Epstein-Barr virus latent genome correlates with the oncogenicity by the activation level of LMP1 and NF-κB

Oncotarget. 2015 Dec 1;6(38):41033-44. doi: 10.18632/oncotarget.5708.

Abstract

A tumor model that Epstein-Barr virus (EBV) latent infection facilitated the tumorigenicity was previously established using the Maxi-EBV system. In the present approach, EBV-lost cell clones demonstrated significantly decreased tumorigenesis. On the other hand, the LMP1 gene in Maxi-EBV genome was replaced by that of nasopharyngeal carcinoma origin. The resultant cell line, 293-1/NL showed much lower malignancy than the original 293-EBV. The result was opposite to our expectation. The change of 293 sublineage cells for EBV harboring also got similar result. To seek the underlying reason, the copy number of EBV genome in all the cell lines was detected. The result indicated that 293-EBV contained about 4.5-fold higher EBV copies than 293-1/NL did. Parallel EBV genomes led to relatively stable copies in different 293 sublineages, suggesting the viral genome structure is a factor for the sustainability of EBV's copy number. Moreover, the LMP1 transcription in high copy-containing cells showed abnormally high level. Furthermore, the main LMP1-driven pathway, transcription factor NF-κB, was highly activated in high-copy cells. Here we first manifest by experimental model that the copy number of EBV latent genome correlates with the viral pathogenesis, which depends on the activation level of LMP1 and NF-κB. Overall, both the presence and amount of EBV genome are crucial for the viral oncogenicity.

Keywords: Epstein-Barr virus; copy number; latent genome; latent membrane protein 1; oncogenicity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Transformation, Neoplastic / metabolism*
  • Gene Dosage
  • Gene Expression Regulation, Viral
  • Genome, Viral / genetics
  • HEK293 Cells
  • Herpesvirus 4, Human / genetics
  • Herpesvirus 4, Human / metabolism*
  • Herpesvirus 4, Human / physiology
  • Host-Pathogen Interactions
  • Humans
  • Mice, Inbred BALB C
  • Mice, Nude
  • NF-kappa B / metabolism*
  • Neoplasms, Experimental / metabolism
  • Neoplasms, Experimental / pathology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Transplantation, Heterologous
  • Tumor Burden
  • Viral Matrix Proteins / genetics
  • Viral Matrix Proteins / metabolism*
  • Viral Matrix Proteins / physiology
  • Virus Latency / genetics

Substances

  • EBV-associated membrane antigen, Epstein-Barr virus
  • NF-kappa B
  • Viral Matrix Proteins