Nicotine enhances migration and invasion of human esophageal squamous carcinoma cells which is inhibited by nimesulide

World J Gastroenterol. 2009 May 28;15(20):2500-5. doi: 10.3748/wjg.15.2500.

Abstract

Aim: To study the effect of nicotine on the migration and invasion of human esophageal squamous carcinoma cells and to investigate whether nimesulide can inhibit the effect of nicotine.

Methods: The esophageal squamous carcinoma cell line (TE-13) was treated with different concentrations of nicotine (100 microg/mL and 200 microg/mL) or 200 microg/mL nicotine plus 100 micromol/L nimesulide. Cell migration and invasion were measured using migration and invasion chamber systems. COX-2 expression was determined by Western blotting. Matrix metalloproteinase-2 (MMP-2) was analyzed by zymography and ELISA.

Results: Nicotine (100 microg/mL, 200 microg/mL) enhanced TE-13 cells migration and invasion, and increased the protein expression of COX-2 and the activity of MMP-2. Nicotine (200 microg/mL) stimulated TE-13 cells migration and invasion which were partly blocked by nimesulide. This was associated with decreased protein expression of COX-2 and decreased activity and protein expression of MMP-2.

Conclusion: Nicotine enhances the migration and invasion of the esophageal squamous carcinoma cell line, and nimesulide partly blocks the effect of nicotine-enhanced esophageal squamous carcinoma cell migration and invasion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Calcium Channel Blockers / pharmacology
  • Carcinoma, Squamous Cell* / metabolism
  • Carcinoma, Squamous Cell* / pathology
  • Cell Line, Tumor / drug effects
  • Cell Movement / drug effects*
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Esophageal Neoplasms* / metabolism
  • Esophageal Neoplasms* / pathology
  • Humans
  • Matrix Metalloproteinase 2 / metabolism
  • Neoplasm Invasiveness / pathology*
  • Nicotine / pharmacology*
  • Nicotinic Agonists / pharmacology*
  • Smoking / adverse effects
  • Sulfonamides / pharmacology*

Substances

  • Calcium Channel Blockers
  • Nicotinic Agonists
  • Sulfonamides
  • Nicotine
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Matrix Metalloproteinase 2
  • nimesulide