Inhibition of cyclooxygenase-1 lowers proliferation and induces macroautophagy in colon cancer cells

Biochem Biophys Res Commun. 2009 Apr 24;382(1):79-84. doi: 10.1016/j.bbrc.2009.02.140. Epub 2009 Mar 1.

Abstract

Evolving evidence supports that cyclooxygenase-1 (COX-1) takes part in colon carcinogenesis. The effects of COX-1 inhibition on colon cancer cells, however, remains obscured. In this study, we demonstrate that COX-1 inhibitor sc-560 inhibited colon cancer cell proliferation with concomitant G(0)/G(1)-phase cell cycle arrest. The anti-proliferative effect was associated with down-regulation of c-Fos, cyclin E(2) and E(2)F-1 and up-regulation of p21(Waf1/Cip1) and p27(Kip1). In addition, sc-560 induced macroautophagy, an emerging mechanism of tumor suppression, as evidenced by the formation of LC3(+) autophagic vacuoles, enhanced LC3 processing, and the accumulation of acidic vesicular organelles and autolysosomes. In this connection, 3-methyladenine, a Class III phosphoinositide 3-kinase inhibitor, significantly abolished the formation of LC3(+) autophagic vacuoles and the processing of LC3 induced by sc-560. To conclude, this study reveals the unreported relationship between COX-1 and proliferation/macroautophagy of colon cancer cells.

MeSH terms

  • Adenine / analogs & derivatives
  • Adenine / pharmacology
  • Autophagy* / drug effects
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Colonic Neoplasms / enzymology*
  • Colonic Neoplasms / pathology*
  • Cyclooxygenase 1 / metabolism*
  • Cyclooxygenase Inhibitors / pharmacology
  • Humans
  • Microtubule-Associated Proteins / metabolism
  • Pyrazoles / pharmacology
  • Vacuoles / metabolism

Substances

  • Cyclooxygenase Inhibitors
  • MAP1LC3A protein, human
  • Microtubule-Associated Proteins
  • Pyrazoles
  • SC 560
  • 3-methyladenine
  • Cyclooxygenase 1
  • Adenine