Spontaneous production of interleukin-8 by human lung cancer cells and its augmentation by tumor necrosis factor alpha and interleukin-1 at protein and mRNA levels

Oncology. 1994 Sep-Oct;51(5):467-71. doi: 10.1159/000227385.

Abstract

A cell-to-cell interaction between tumors and host inflammatory cells is important for the subsequent cancer progression or regression. We examined the expression of interleukin-8 (IL-8) mRNAs by 9 human lung cancer cell lines and the influences of cytokines on IL-8 production and its gene expression. Substantial expressions of IL-8 gene were detected in 3 lung cancer cell lines (RERF-LC-OK, Lu-134-A-H, YO-88 cells). Moreover, 4 lung cancer cell lines (RERF-LC-MS, RERF-LC-OK, A549 and YO-88) were used to examine the effects of exogenous cytokines--interleukin-1 beta (IL-1 beta), tumor necrosis factor alpha (TNF-alpha) and granulocyte-macrophage colony-stimulating factor--on IL-8 production by the cells at protein and gene levels. TNF-alpha and IL-1 beta significantly augmented the levels of mRNA expression for IL-8 and its production. These observations indicate that tumor-derived IL-8 may be important in recruiting inflammatory neutrophils and promoting interaction between lung cancer and inflammatory cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Interleukin-1 / pharmacology*
  • Interleukin-8 / biosynthesis*
  • Lung Neoplasms / metabolism*
  • RNA, Messenger / biosynthesis*
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Interleukin-1
  • Interleukin-8
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha