GMI, a fungal immunomodulatory protein from Ganoderma microsporum, induce apoptosis via β-catenin suppression in lung cancer cells

Environ Toxicol. 2018 Sep;33(9):955-961. doi: 10.1002/tox.22582. Epub 2018 Jul 4.

Abstract

β-catenin is important in development of lung cancer. In our previous study, GMI, a fungal immunomodulatory protein, inhibits lung cancer cell survival. The aim of this study is to evaluate the effect of GMI on β-catenin inhibition and apoptosis induction. GMI induced apoptosis in lung cancer cells bearing wild-type and mutated EGFR. GMI did not reduce the β-catenin mRNA expression but suppressed the protein expressions of β-catenin that resulted in the transcriptional downregulation of its target genes: survivin and cyclin-D1. The transcriptional activation activity of β-catenin was demonstrated by TOPFLASH/FOPFLASH luciferase reporter assay. Inhibition of GSK-3β and proteasome blocked the inhibiting effect of GMI on β-catenin and its target genes. β-catenin silencing increased activation of apoptosis in GMI-treated H1355 cells. This is the first study to reveal the novel function of GMI in inducing apoptosis via β-catenin inhibition. These results provide a new potential of GMI in against lung cancer.

Keywords: GMI; apoptosis; fungal immunomodulatory protein; lung cancer; β-catenin.

MeSH terms

  • Apoptosis / drug effects*
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Down-Regulation
  • Fungal Proteins / pharmacology*
  • Ganoderma / metabolism*
  • Glycogen Synthase Kinase 3 beta / metabolism
  • Humans
  • Immunologic Factors / pharmacology*
  • Lung Neoplasms / pathology*
  • beta Catenin / antagonists & inhibitors*
  • beta Catenin / metabolism

Substances

  • CTNNB1 protein, human
  • Fungal Proteins
  • Immunologic Factors
  • beta Catenin
  • Glycogen Synthase Kinase 3 beta