Targeting multiple signaling pathways by green tea polyphenol (-)-epigallocatechin-3-gallate

Cancer Res. 2006 Mar 1;66(5):2500-5. doi: 10.1158/0008-5472.CAN-05-3636.

Abstract

Cell signaling pathways, responsible for maintaining a balance between cell proliferation and death, have emerged as rational targets for the management of cancer. Emerging data amassed from various laboratories around the world suggests that green tea, particularly its major polyphenolic constituent (-)-epigallocatechin-3-gallate (EGCG), possesses remarkable cancer chemopreventive and therapeutic potential against various cancer sites in animal tumor bioassay systems and in some human epidemiologic studies. EGCG has been shown to modulate multiple signal transduction pathways in a fashion that controls the unwanted proliferation of cells, thereby imparting strong cancer chemopreventive as well as therapeutic effects. This review discusses the modulations of important signaling events by EGCG and their implications in cancer management.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Anticarcinogenic Agents / pharmacology*
  • Anticarcinogenic Agents / therapeutic use
  • Apoptosis / drug effects
  • Catechin / analogs & derivatives*
  • Catechin / pharmacology
  • Catechin / therapeutic use
  • Cell Cycle / drug effects
  • Clinical Trials as Topic
  • ErbB Receptors / antagonists & inhibitors
  • Humans
  • MAP Kinase Signaling System / drug effects
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • NF-kappa B / antagonists & inhibitors
  • Neovascularization, Pathologic / drug therapy
  • Protease Inhibitors / pharmacology*
  • Protease Inhibitors / therapeutic use
  • Receptor, IGF Type 1 / antagonists & inhibitors
  • Signal Transduction / drug effects*
  • Tea
  • Vascular Endothelial Growth Factor A / antagonists & inhibitors

Substances

  • Anticarcinogenic Agents
  • NF-kappa B
  • Protease Inhibitors
  • Tea
  • Vascular Endothelial Growth Factor A
  • Catechin
  • epigallocatechin gallate
  • ErbB Receptors
  • Receptor, IGF Type 1
  • Mitogen-Activated Protein Kinases