The role of peroxiredoxin V in (-)-epigallocatechin 3-gallate-induced multiple myeloma cell death

Oncol Res. 2011;19(8-9):391-8. doi: 10.3727/096504011x13127606672922.

Abstract

(-)-Epigallocatechin 3-gallate (EGCG) is a potent antioxidant polyphenol in green tea that acts as an anticancer agent via both direct and indirect pathways. Although the relationship between EGCG's anticancer effects and its antioxidant activity is not fully understood, it is known that EGCG stimulates production of reactive oxygen species (ROS), which induce oxidative stress leading to cell death. In IM9 multiple myeloma cells, EGCG acted in a dose- and time-dependent manner to induce apoptotic cell death. Among the antioxidant enzymes expressed in IM9 cells, levels of peroxiredoxin V (PrdxV) were selectively and significantly reduced by EGCG. Moreover, the ROS scavenger NAC completely inhibited EGCG-induced apoptosis and PrdxV reduction, while overexpression of PrdxV, but not a Prdx(VC48S) mutant, protected IM9 cells from EGCG-induced apoptosis. EGCG-induced reductions in cell viability and PrdxV levels were also observed in primary CD138+ multiple myeloma cells from patients. These results suggest that PrdxV is a key target via which EGCG mediates its anticancer effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcysteine / pharmacology
  • Apoptosis / drug effects*
  • Catechin / analogs & derivatives*
  • Catechin / pharmacology
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Humans
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Multiple Myeloma / enzymology*
  • Peroxiredoxins / drug effects*
  • Peroxiredoxins / metabolism
  • Phosphorylation / drug effects
  • Plasma Cells / drug effects
  • Plasma Cells / immunology
  • Reactive Oxygen Species
  • Signal Transduction / drug effects*
  • Syndecan-1
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Reactive Oxygen Species
  • Syndecan-1
  • Catechin
  • epigallocatechin gallate
  • Peroxiredoxins
  • Extracellular Signal-Regulated MAP Kinases
  • JNK Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Acetylcysteine