Glabridin inhibits migration, invasion, and angiogenesis of human non-small cell lung cancer A549 cells by inhibiting the FAK/rho signaling pathway

Integr Cancer Ther. 2011 Dec;10(4):341-9. doi: 10.1177/1534735410384860. Epub 2010 Nov 8.

Abstract

This study reports the antimigration, anti-invasive effect of glabridin, a flavonoid obtained from licorice, in human non-small cell lung cancer A549 cells. Glabridin exhibited effective inhibition of cell metastasis by decreasing cancer cell migration and invasion of A549 cells. In addition, glabridin also decreased A549-mediated angiogenesis. Further investigation revealed that glabridin's inhibition of cancer angiogenesis was also evident in a nude mice model. Blockade of A549 cells migration was associated with an increase of ανβ3 integrin proteosome degradation. Glabridin also decreased the active forms of FAK and Src, and enhanced levels of inactivated phosphorylated Src (Tyr 527), decreasing the interaction of FAK and Src. Inhibition of the FAK/Src complex by glabridin also blocked Akt activation, resulting in reduced activation of RhoA and myosin light chain phosphorylation. This study demonstrates that glabridin may be a novel anticancer agent for the treatment of lung cancer in 3 different ways: inhibition of migration, invasion, and angiogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carcinoma, Non-Small-Cell Lung / enzymology
  • Carcinoma, Non-Small-Cell Lung / metabolism*
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Epithelial-Mesenchymal Transition / drug effects
  • Focal Adhesion Protein-Tyrosine Kinases / drug effects*
  • Focal Adhesion Protein-Tyrosine Kinases / metabolism
  • Humans
  • Integrin beta3 / drug effects
  • Integrin beta3 / metabolism
  • Isoflavones / pharmacology*
  • Lung Neoplasms / enzymology
  • Lung Neoplasms / metabolism*
  • Mice
  • Mice, Nude
  • Myosin Light Chains / metabolism
  • Neovascularization, Pathologic / enzymology
  • Neovascularization, Pathologic / metabolism
  • Phenols / pharmacology*
  • Phosphorylation / drug effects
  • Signal Transduction / drug effects*
  • rhoA GTP-Binding Protein / drug effects*
  • rhoA GTP-Binding Protein / metabolism
  • src-Family Kinases / drug effects
  • src-Family Kinases / metabolism

Substances

  • Integrin beta3
  • Isoflavones
  • Myosin Light Chains
  • Phenols
  • Focal Adhesion Protein-Tyrosine Kinases
  • src-Family Kinases
  • rhoA GTP-Binding Protein
  • glabridin