An NF-kappaB gene expression signature contributes to Kaposi's sarcoma virus vGPCR-induced direct and paracrine neoplasia

Oncogene. 2008 Mar 20;27(13):1844-52. doi: 10.1038/sj.onc.1210817. Epub 2007 Oct 15.

Abstract

Kaposi's sarcoma (KS) is the most frequent AIDS-associated malignancy, etiologically linked to the infection with the human herpesvirus 8 (HHV-8/KSHV). This member of the gamma-herpesviridae family encodes 81 open reading frames, several bearing oncogenic potential. A constitutively active virally encoded G protein-coupled receptor (vGPCR) readily induces KS-like lesions when expressed in endothelial cells in vivo, and unmasks the oncogenic potential of other HHV-8 genes in a paracrine fashion. How vGPCR causes endothelial cell transformation is still not fully understood. Using full-genome microarray analysis we show here that the expression of nuclear factor-kappaB (NF-kappaB)-regulated genes is a prominent feature triggered by vGPCR in cells expressing this viral oncogene and in cells exposed to vGPCR-induced secretions, thus mimicking its paracrine effect. Indeed, vGPCR activates the NF-kappaB pathway potently, and NF-kappaB activation is a hallmark of both human and experimental KS. Of interest, whereas constitutive NF-kappaB signaling is not sufficient to promote endothelial cells transformation, NF-kappaB function is strictly required for vGPCR-induced direct and paracrine neoplasia. Taken together, these results strongly support the role of NF-kappaB regulated genes in KS pathogenesis, thus providing the rationale for the development of novel mechanism-based therapies for this angioproliferative disease.

Publication types

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

MeSH terms

  • Animals
  • Cell Transformation, Neoplastic*
  • Cells, Cultured
  • Endothelium, Vascular / pathology*
  • Fluorescent Antibody Technique
  • Gene Expression Profiling*
  • Herpesvirus 8, Human / pathogenicity*
  • Humans
  • Immunoblotting
  • Mice
  • Mice, Nude
  • NF-kappa B / genetics*
  • Oligonucleotide Array Sequence Analysis
  • Paracrine Communication*
  • Receptors, Chemokine / metabolism*
  • Sarcoma, Kaposi / genetics
  • Sarcoma, Kaposi / metabolism*
  • Sarcoma, Kaposi / pathology
  • Synaptotagmin I / metabolism
  • Transplantation, Heterologous

Substances

  • G protein-coupled receptor, Human herpesvirus 8
  • NF-kappa B
  • Receptors, Chemokine
  • Synaptotagmin I