Integrated in silico and experimental methods revealed that Arctigenin inhibited angiogenesis and HCT116 cell migration and invasion through regulating the H1F4A and Wnt/β-catenin pathway

Mol Biosyst. 2015 Nov;11(11):2878-84. doi: 10.1039/c5mb00439j.

Abstract

Arctigenin (ARG) has been previously reported to exert diverse biological activities including anti-proliferation, anti-inflammatory, and antiviral, etc. In the current study, the anti-metastasis and anti-angiogenesis activities of ARG were investigated. To further understand how ARG played these bioactivities, proteomic approaches were used to profile the proteome changes in response to ARG treatment using 2DE-MS/MS. Using these approaches, a total of 50 differentially expressed proteins were identified and clustered. Bioinformatics analysis suggested that multiple signalling pathways were involved. Moreover, ARG induced anti-metastatic and anti-angiogenesis activities were mainly accompanied by a deactivation of the Wnt/β-catenin pathway in HCT116 cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Animals, Genetically Modified
  • Cell Movement* / drug effects
  • Cell Proliferation / drug effects
  • Computational Biology
  • Computer Simulation*
  • Furans / chemistry
  • Furans / pharmacology
  • Furans / therapeutic use*
  • HCT116 Cells
  • Histones / metabolism*
  • Human Umbilical Vein Endothelial Cells / drug effects
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Lignans / chemistry
  • Lignans / pharmacology
  • Lignans / therapeutic use*
  • Molecular Sequence Data
  • Neoplasm Invasiveness
  • Neovascularization, Pathologic / drug therapy*
  • Protein Interaction Maps / drug effects
  • Proteomics
  • Wnt Signaling Pathway* / drug effects
  • Wound Healing / drug effects
  • Zebrafish / genetics

Substances

  • Furans
  • Histones
  • Lignans
  • arctigenin