Inositol induces mesenchymal-epithelial reversion in breast cancer cells through cytoskeleton rearrangement

Exp Cell Res. 2016 Jul 1;345(1):37-50. doi: 10.1016/j.yexcr.2016.05.007. Epub 2016 May 26.

Abstract

Inositol displays multi-targeted effects on many biochemical pathways involved in epithelial-mesenchymal transition (EMT). As Akt activation is inhibited by inositol, we investigated if such effect could hamper EMT in MDA-MB-231 breast cancer cells. In cancer cells treated with pharmacological doses of inositol E-cadherin was increased, β-catenin was redistributed behind cell membrane, and metalloproteinase-9 was significantly reduced, while motility and invading capacity were severely inhibited. Those changes were associated with a significant down-regulation of PI3K/Akt activity, leading to a decrease in downstream signaling effectors: NF-kB, COX-2, and SNAI1. Inositol-mediated inhibition of PS1 leads to lowered Notch 1 release, thus contributing in decreasing SNAI1 levels. Overall, these data indicated that inositol inhibits the principal molecular pathway supporting EMT. Similar results were obtained in ZR-75, a highly metastatic breast cancer line. These findings are coupled with significant changes on cytoskeleton. Inositol slowed-down vimentin expression in cells placed behind the wound-healing edge and stabilized cortical F-actin. Moreover, lamellipodia and filopodia, two specific membrane extensions enabling cell migration and invasiveness, were no longer detectable after inositol addiction. Additionally, fascin and cofilin, two mandatory required components for F-actin assembling within cell protrusions, were highly reduced. These data suggest that inositol may induce an EMT reversion in breast cancer cells, suppressing motility and invasiveness through cytoskeleton modifications.

Keywords: Cytoskeleton; EMT; Inositol; Invasion; MET; Motility.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyloid Precursor Protein Secretases / metabolism
  • Breast Neoplasms / pathology*
  • Cadherins / metabolism
  • Carrier Proteins / metabolism
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cytoskeleton / drug effects
  • Cytoskeleton / pathology*
  • Down-Regulation / drug effects
  • Enzyme Activation / drug effects
  • Epithelial Cells / drug effects
  • Epithelial Cells / pathology*
  • Female
  • Humans
  • Immunoblotting
  • Inositol / pharmacology*
  • Mesoderm / drug effects
  • Mesoderm / pathology*
  • Microfilament Proteins / metabolism
  • NF-kappa B / metabolism
  • Neoplasm Invasiveness
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphorylation / drug effects
  • Presenilin-1 / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Vimentin / metabolism
  • Wound Healing / drug effects
  • beta Catenin / metabolism
  • rho-Associated Kinases / metabolism

Substances

  • Cadherins
  • Carrier Proteins
  • FSCN1 protein, human
  • Microfilament Proteins
  • NF-kappa B
  • Presenilin-1
  • Vimentin
  • beta Catenin
  • Inositol
  • Phosphatidylinositol 3-Kinases
  • Proto-Oncogene Proteins c-akt
  • rho-Associated Kinases
  • Amyloid Precursor Protein Secretases