Expression of RANTES and MCP-1 in epithelial cells is regulated via LMP1 and CD40

Int J Cancer. 2007 Dec 15;121(12):2703-10. doi: 10.1002/ijc.23018.

Abstract

Epstein-Barr virus (EBV)-associated undifferentiated nasopharyngeal carcinoma (NPC) is characterized by a prominent nonneoplastic lymphoid stroma. The functional role of these inflammatory cells and the mechanism of their recruitment are not fully understood. In B-cells, the EBV-encoded latent membrane protein 1 (LMP1) can induce the expression of chemokines in an NF-kappaB dependent manner. We now show that LMP1 can induce the expression of RANTES and MCP-1 in an epithelial cell line, and that this effect is partially reversible by an inhibitor of NF-kappaB. Since tumor cells of virtually all NPCs show CD40 expression while many cases are LMP1-negative at the protein level, we also investigated the effect of CD40 signaling and demonstrate that CD40 stimulation can transiently induce RANTES and MCP-1 expression in LMP1-negative epithelial cells. In in situ hybridization only rare tumor cells showed expression of these chemokines unrelated to LMP1 expression, a pattern consistent with transient induction through CD40 signaling. Since RANTES and MCP-1 were also detected in the neoplastic cells of oral squamous cell carcinomas lacking a lymphoid stroma it remains uncertain to what extent these CC chemokines contribute to the attraction of inflammatory cells into the NPC microenvironment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD40 Antigens / metabolism*
  • Carcinoma, Squamous Cell / metabolism*
  • Carcinoma, Squamous Cell / virology
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / metabolism*
  • Chemokine CCL5 / metabolism*
  • Gene Expression Regulation, Neoplastic
  • Head and Neck Neoplasms / metabolism*
  • Head and Neck Neoplasms / virology
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • NF-kappa B / metabolism
  • Oncogene Proteins, Viral / metabolism
  • RNA, Messenger / metabolism
  • Signal Transduction
  • Up-Regulation
  • Viral Matrix Proteins / metabolism*

Substances

  • CCL2 protein, human
  • CD40 Antigens
  • Chemokine CCL2
  • Chemokine CCL5
  • EBV-associated membrane antigen, Epstein-Barr virus
  • NF-kappa B
  • Oncogene Proteins, Viral
  • RNA, Messenger
  • Viral Matrix Proteins