Amorfrutin A inhibits TNF-α-induced NF-κB activation and NF-κB-regulated target gene products

Int Immunopharmacol. 2014 Jul;21(1):56-62. doi: 10.1016/j.intimp.2014.04.016. Epub 2014 Apr 28.

Abstract

The nuclear factor-κB (NF-κB) transcription factors control many physiological processes including inflammation, immunity, apoptosis, and angiogenesis. In our search for NF-κB inhibitors from natural resources, we identified amorfrutin A as an inhibitor of NF-κB activation from the fruits of Amorpha fruticosa L. In present study, this compound significantly inhibited the TNF-α-induced expression of NF-κB reporter gene. Further analysis revealed that amorfrutin A was a potent inhibitor of NF-κB activation by the suppression of TNF-α-induced inhibitor of κBα (IκBα) degradation, p65 nuclear translocation, and DNA-binding activity of NF-κB. We also demonstrated that pretreatment of cells with this compound prevented the TNF-α-induced expression of NF-κB target genes, such as antiapoptosis (cIAP-1 and FLIP), proliferation (COX-2 and cyclinD1), invasion (MMP-9), angiogenesis (VEGF), and major inflammatory cytokines (TNF-α, IL-8, and MCP1). Furthermore, our results suggest that amorfrutin A potentiates TNF-α-induced apoptosis. Taken together, amorfrutin A could be a valuable candidate for the intervention of NF-κB-dependent pathological conditions such as inflammation.

Keywords: Amorfrutin A; Apoptosis; Inflammation; IκBα; Nuclear factor-κB (NF-κB).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus / drug effects
  • CASP8 and FADD-Like Apoptosis Regulating Protein / genetics
  • CASP8 and FADD-Like Apoptosis Regulating Protein / metabolism
  • Cell Nucleus / metabolism*
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / metabolism
  • Cyclin D1 / genetics
  • Cyclin D1 / metabolism
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Fabaceae / immunology*
  • Gene Expression Regulation / drug effects
  • HeLa Cells
  • Humans
  • Inhibitor of Apoptosis Proteins / genetics
  • Inhibitor of Apoptosis Proteins / metabolism
  • Interleukin-8 / genetics
  • Interleukin-8 / metabolism
  • Matrix Metalloproteinase 9 / genetics
  • Matrix Metalloproteinase 9 / metabolism
  • NF-kappa B / metabolism*
  • Salicylates / pharmacology*
  • Stilbenes / pharmacology
  • Tumor Necrosis Factor-alpha / immunology
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism
  • eIF-2 Kinase / metabolism*

Substances

  • CASP8 and FADD-Like Apoptosis Regulating Protein
  • CCL2 protein, human
  • Chemokine CCL2
  • Inhibitor of Apoptosis Proteins
  • Interleukin-8
  • NF-kappa B
  • Salicylates
  • Stilbenes
  • Tumor Necrosis Factor-alpha
  • Vascular Endothelial Growth Factor A
  • amorfrutin A
  • Cyclin D1
  • Cyclooxygenase 2
  • eIF-2 Kinase
  • Matrix Metalloproteinase 9