PUBLICATION

Raddeanin A, a triterpenoid saponin isolated from Anemone raddeana, suppresses the angiogenesis and growth of human colorectal tumor by inhibiting VEGFR2 signaling

Authors
Guan, Y.Y., Liu, H.J., Luan, X., Xu, J.R., Lu, Q., Liu, Y.R., Gao, Y.G., Zhao, M., Chen, H.Z., Fang, C.
ID
ZDB-PUB-150201-5
Date
2015
Source
Phytomedicine : international journal of phytotherapy and phytopharmacology   22: 103-10 (Journal)
Registered Authors
Keywords
Anemone raddeana, Colorectal tumor, Raddeanin A, Tumor angiogenesis, VEGFR2, Zebrafish
MeSH Terms
  • Anemone/chemistry*
  • Angiogenesis Inhibitors/pharmacology*
  • Animals
  • Antineoplastic Agents, Phytogenic/pharmacology*
  • Cell Line, Tumor
  • Chick Embryo
  • Colorectal Neoplasms/pathology
  • Female
  • Human Umbilical Vein Endothelial Cells/drug effects
  • Humans
  • Mice
  • Mice, Inbred BALB C
  • Molecular Docking Simulation
  • Neovascularization, Pathologic/prevention & control
  • Saponins/pharmacology*
  • Signal Transduction/drug effects*
  • Vascular Endothelial Growth Factor Receptor-2/metabolism*
  • Xenograft Model Antitumor Assays
  • Zebrafish/embryology
PubMed
25636878 Full text @ Phytomedicine
Abstract
Raddeanin A (RA) is an active triterpenoid saponin from a traditional Chinese medicinal herb, Anemone raddeana Regel. It was previously reported that RA possessed attractive antitumor activity through inhibiting proliferation and inducing apoptosis of multiple cancer cells. However, whether RA can inhibit angiogenesis, an essential step in cancer development, remains unknown. In this study, we found that RA could significantly inhibit human umbilical vein endothelial cell (HUVEC) proliferation, motility, migration, and tube formation. RA also dramatically reduced angiogenesis in chick embryo chorioallantoic membrane (CAM), restrained the trunk angiogenesis in zebrafish, and suppressed angiogenesis and growth of human HCT-15 colorectal cancer xenograft in mice. Western blot assay showed that RA suppressed VEGF-induced phosphorylation of VEGFR2 and its downstream protein kinases including PLCγ1, JAK2, FAK, Src, and Akt. Molecular docking simulation indicated that RA formed hydrogen bonds and hydrophobic interactions within the ATP binding pocket of VEGFR2 kinase domain. Our study firstly provides the evidence that RA has high antiangiogenic potency and explores its molecular basis, demonstrating that RA is a potential agent or lead candidate for antiangiogenic cancer therapy.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping