Human herpesvirus-encoded kinase induces B cell lymphomas in vivo

J Clin Invest. 2018 Jun 1;128(6):2519-2534. doi: 10.1172/JCI97053. Epub 2018 May 7.

Abstract

Kaposi's sarcoma-associated herpesvirus (KSHV) is a gammaherpesvirus that is the etiological agent of the endothelial cell cancer Kaposi's sarcoma (KS) and 2 B cell lymphoproliferative disorders, primary effusion lymphoma (PEL) and multicentric Castleman's disease (MCD). KSHV ORF36, also known as viral protein kinase (vPK), is a viral serine/threonine kinase. We previously reported that KSHV vPK enhances cell proliferation and mimics cellular S6 kinase to phosphorylate ribosomal protein S6, a protein involved in protein synthesis. We created a mouse model to analyze the function of vPK in vivo. We believe this is the first mouse tumor model of a viral kinase encoded by a pathogenic human virus. We observed increased B cell activation in the vPK transgenic mice compared with normal mice. We also found that, over time, vPK transgenic mice developed a B cell hyperproliferative disorder and/or a high-grade B cell non-Hodgkin lymphoma at a greatly increased incidence compared with littermate controls. This mouse model shows that a viral protein kinase is capable of promoting B cell activation and proliferation as well as augmenting lymphomagenesis in vivo and may therefore contribute to the development of viral cancers.

Keywords: Lymphomas; Oncogenes; Oncology; Virology.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Castleman Disease / enzymology
  • Castleman Disease / genetics
  • Castleman Disease / pathology
  • Castleman Disease / virology
  • Cell Transformation, Viral*
  • Herpesvirus 8, Human / enzymology*
  • Herpesvirus 8, Human / genetics
  • Humans
  • Lymphoma, Primary Effusion / enzymology*
  • Lymphoma, Primary Effusion / genetics
  • Lymphoma, Primary Effusion / pathology
  • Lymphoma, Primary Effusion / virology
  • Mice
  • Mice, Transgenic
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism*
  • Protein Kinases / genetics
  • Protein Kinases / metabolism*

Substances

  • Neoplasm Proteins
  • Protein Kinases
  • ORF36 protein kinase, Kaposi's sarcoma herpesvirus

Supplementary concepts

  • Multi-centric Castleman's Disease