Galectin-1 induces invasion and the epithelial-mesenchymal transition in human gastric cancer cells via non-canonical activation of the hedgehog signaling pathway

Oncotarget. 2016 Dec 13;7(50):83611-83626. doi: 10.18632/oncotarget.13201.

Abstract

Galectin-1 (Gal-1) has been reported to be an independent prognostic indicator of poor survival in gastric cancer and overexpression of Gal-1 enhances the invasiveness of gastric cancer cells. However, the downstream mechanisms by which Gal-1 promotes invasion remains unclear. Moreover, the function of Gal-1 in the epithelial-mesenchymal transition (EMT) in gastric cancer has not yet been elucidated. In this study, we observed Gal-1 expression was upregulated and positively associated with metastasis and EMT markers in 162 human gastric cancer tissue specimens. In vitro studies showed Gal-1 induced invasion, the EMT phenotype and activated the non-canonical hedgehog (Hh) pathway in gastric cancer cell lines. Furthermore, our data revealed that Gal-1 modulated the non-canonical Hh pathway by increasing the transcription of glioma-associated oncogene-1 (Gli-1) via a Smoothened (SMO)-independent manner, and that upregulation of Gal-1 was strongly associated with gastric cancer metastasis. We conclude that Gal-1 promotes invasion and the EMT in gastric cancer cells via activation of the non-canonical Hh pathway, suggesting Gal-1 could represent a promising therapeutic target for the prevention and treatment of gastric cancer metastasis.

Keywords: Gli-1; epithelial-mesenchymal transition; galectin-1; gastric cancer; hedgehog signaling.

MeSH terms

  • Cell Line, Tumor
  • Cell Movement*
  • Epithelial-Mesenchymal Transition*
  • Female
  • Galectin 1 / genetics
  • Galectin 1 / metabolism*
  • Hedgehog Proteins / metabolism*
  • Humans
  • Male
  • Middle Aged
  • Neoplasm Invasiveness
  • Phenotype
  • RNA Interference
  • Signal Transduction*
  • Smoothened Receptor / genetics
  • Smoothened Receptor / metabolism
  • Stomach Neoplasms / genetics
  • Stomach Neoplasms / metabolism*
  • Stomach Neoplasms / pathology
  • Transfection
  • Up-Regulation
  • Zinc Finger Protein GLI1 / genetics
  • Zinc Finger Protein GLI1 / metabolism

Substances

  • GLI1 protein, human
  • Galectin 1
  • Hedgehog Proteins
  • LGALS1 protein, human
  • SMO protein, human
  • Smoothened Receptor
  • Zinc Finger Protein GLI1