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Antiangiogenic effects of p-coumaric acid in human endothelial cells.

Abstract
p-Coumaric acid, a hydroxy derivative of cinnamic acid, has been known to possess antioxidant and anticancer activities. Despite its potential contribution to chemopreventive effects, the mechanism by which p-coumaric acid exerts its antiangiogenic actions remains elusive. In this study, we revealed that p-coumaric acid inhibited the sprouting of endothelial cells in rat aortic rings and inhibited the tube formation and migration of endothelial cells. We observed that p-coumaric acid could downregulate mRNA expression levels of the key angiogenic factors vascular endothelial growth factor and basic fibroblast growth factor. Also, we demonstrated that p-coumaric acid inhibited both the AKT and ERK signaling pathways, which are known to be crucial for angiogenesis. Using a mouse model, we also showed that p-coumaric acid effectively suppressed tumor growth in vivo by lowering hemoglobin contents. Collectively, these findings indicate that p-coumaric acid possesses potent anticancer properties due to the inhibition of angiogenesis in vivo.
AuthorsChang-Seok Kong, Chul-Ho Jeong, Jae-Sun Choi, Kil-Jung Kim, Joo-Won Jeong
JournalPhytotherapy research : PTR (Phytother Res) Vol. 27 Issue 3 Pg. 317-23 (Mar 2013) ISSN: 1099-1573 [Electronic] England
PMID22585412 (Publication Type: Journal Article)
CopyrightCopyright © 2012 John Wiley & Sons, Ltd
Chemical References
  • Angiogenesis Inhibitors
  • Antineoplastic Agents
  • Coumaric Acids
  • Propionates
  • Reactive Oxygen Species
  • Vascular Endothelial Growth Factor A
  • Fibroblast Growth Factor 2
  • p-coumaric acid
Topics
  • Adenocarcinoma (blood supply)
  • Angiogenesis Inhibitors (pharmacology)
  • Animals
  • Antineoplastic Agents (pharmacology)
  • Aorta (cytology)
  • Cell Line
  • Cell Movement (drug effects)
  • Cell Proliferation (drug effects)
  • Coumaric Acids (pharmacology)
  • Down-Regulation (drug effects)
  • Endothelial Cells (drug effects)
  • Fibroblast Growth Factor 2 (metabolism)
  • Humans
  • In Vitro Techniques
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Neovascularization, Pathologic (drug therapy)
  • Propionates
  • Rats
  • Reactive Oxygen Species (metabolism)
  • Signal Transduction (drug effects)
  • Vascular Endothelial Growth Factor A (metabolism)

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