PUBLICATION

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

Authors
Zhang, S., Li, J., Song, S., Li, J., Tong, R., Zang, Z., Jiang, Q., Cai, L.
ID
ZDB-PUB-170214-138
Date
2015
Source
Molecular Biosystems   11: 2878-84 (Journal)
Registered Authors
Li, Jie
Keywords
none
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
PubMed
26267229 Full text @ Mol. Biosyst.
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.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping