Effects of galectin-9 on apoptosis, cell cycle and autophagy in human esophageal adenocarcinoma cells

Oncol Rep. 2017 Jul;38(1):506-514. doi: 10.3892/or.2017.5689. Epub 2017 Jun 1.

Abstract

The incidence of esophageal adenocarcinoma (EAC) is rapidly increasing in western countries. The overall mortality of this disease remains high with a 5-year survival rate of less than 20%, despite remarkable advances in the care of patients with EAC. Galectin-9 (Gal-9) is a tandem-repeat type galectin that exerts anti-proliferative effects on various cancer cell types. The aim of the present study was to evaluate the effects of Gal-9 on human EAC cells and to assess the expression of microRNAs (miRNAs) associated with the antitumor effects of Gal-9 in vitro. Gal-9 suppressed the proliferation of the EAC cell lines OE19, OE33, SK-GT4, and OACM 5.1C. Additionally, Gal-9 treatment induced apoptosis and increased the expression levels of caspase-cleaved cytokeratin 18, activated caspase-3 and activated caspase-9. However, it did not promote cell cycle arrest by reducing cell cycle-related protein levels. Furthermore, Gal-9 increased the level of the angiogenesis-related protein interleukin-8 (IL-8) and markedly altered miRNA expression. Based on these findings, Gal-9 may be of clinical use for the treatment of EAC.

MeSH terms

  • Adenocarcinoma / drug therapy*
  • Adenocarcinoma / genetics*
  • Adenocarcinoma / pathology
  • Apoptosis / drug effects
  • Autophagy
  • Caspase 3 / metabolism
  • Caspase 9 / metabolism
  • Cell Cycle Checkpoints / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Esophageal Neoplasms / drug therapy*
  • Esophageal Neoplasms / genetics*
  • Esophageal Neoplasms / pathology
  • Galectins / genetics
  • Galectins / pharmacology*
  • Galectins / therapeutic use
  • Gene Expression Profiling
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Humans
  • Interleukin-8 / metabolism
  • Keratin-18 / metabolism
  • MicroRNAs / isolation & purification
  • MicroRNAs / metabolism*
  • Mutation
  • Oligonucleotide Array Sequence Analysis
  • Recombinant Proteins / pharmacology
  • Recombinant Proteins / therapeutic use

Substances

  • CXCL8 protein, human
  • Galectins
  • Interleukin-8
  • KRT18 protein, human
  • Keratin-18
  • LGALS9 protein, human
  • MicroRNAs
  • Recombinant Proteins
  • CASP3 protein, human
  • CASP9 protein, human
  • Caspase 3
  • Caspase 9

Supplementary concepts

  • Adenocarcinoma Of Esophagus