Heterogeneity among human nasopharyngeal carcinoma cell lines for inflammatory cytokines mRNA expression levels

Biochem Biophys Res Commun. 1992 Aug 31;187(1):121-6. doi: 10.1016/s0006-291x(05)81467-6.

Abstract

Using polymerase chain reaction (PCR), we confirmed the expression of interleukin-1 alpha (IL-1 alpha) by the human nasopharyngeal carcinoma (NPC) cell line C15 without contribution of either human IL-1 beta or mouse IL-1 alpha in the biological activity previously found in C15. However we showed that IL-1 alpha was not expressed in all NPCs. IL-1 beta and/or tumor necrosis factor (TNF)-alpha genes could also be activated, independently from the number of Epstein Barr Virus (EBV) copies harbored by the cells. Interestingly, the primary tumor C15 showed a profile of TNF-sensitive tumor while C17, C18 and C19 which were derived from metastasis have a typical profile of TNF-resistant cells. Furthermore, the inflammatory cytokines whose genes are classically induced by IL-1 and TNF were found expressed only in C17 and C19 suggesting another level of heterogeneity among NPCs.

MeSH terms

  • Animals
  • Base Sequence
  • Chemokine CCL2
  • Chemotactic Factors / genetics
  • Cytokines / genetics*
  • Gene Expression*
  • Genes, Viral
  • Herpesvirus 4, Human / genetics
  • Humans
  • Interleukin-1 / genetics
  • Interleukin-8 / genetics
  • Mice
  • Mice, Nude
  • Molecular Sequence Data
  • Nasopharyngeal Neoplasms / metabolism*
  • Polymerase Chain Reaction
  • RNA, Messenger / metabolism
  • Receptors, Cell Surface / genetics
  • Receptors, Tumor Necrosis Factor
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Chemokine CCL2
  • Chemotactic Factors
  • Cytokines
  • Interleukin-1
  • Interleukin-8
  • RNA, Messenger
  • Receptors, Cell Surface
  • Receptors, Tumor Necrosis Factor
  • Tumor Necrosis Factor-alpha