Quercetin-3-methyl ether suppresses proliferation of mouse epidermal JB6 P+ cells by targeting ERKs

Carcinogenesis. 2012 Feb;33(2):459-65. doi: 10.1093/carcin/bgr281. Epub 2011 Dec 1.

Abstract

Chemoprevention has been acknowledged as an important and practical strategy for the management of skin cancer. Quercetin-3-methyl ether, a naturally occurring compound present in various plants, has potent anticancer-promoting activity. We identified this compound by in silico virtual screening of the Traditional Chinese Medicine Database using extracellular signal-regulated kinase 2 (ERK2) as the target protein. Here, we showed that quercetin-3-methyl ether inhibited proliferation of mouse skin epidermal JB6 P+ cells in a dose- and time-dependent manner by inducing cell cycle G(2)-M phase accumulation. It also suppressed 12-O-tetradecanoylphorbol-13-acetate-induced neoplastic cell transformation in a dose-dependent manner. Its inhibitory effect was greater than quercetin. The activation of activator protein-1 was dose-dependently suppressed by quercetin-3-methyl ether treatment. Western blot and kinase assay data revealed that quercetin-3-methyl ether inhibited ERKs kinase activity and attenuated phosphorylation of ERKs. Pull-down assays revealed that quercetin-3-methyl ether directly binds with ERKs. Furthermore, a loss-of-function ERK2 mutation inhibited the effectiveness of the quercetin-3-methyl ether. Overall, these results indicated that quercetin-3-methyl ether exerts potent chemopreventive activity by targeting ERKs.

Publication types

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

MeSH terms

  • Animals
  • Cell Cycle / drug effects
  • Cell Cycle Checkpoints / drug effects
  • Cell Proliferation / drug effects
  • Cell Transformation, Neoplastic / drug effects
  • Cells, Cultured
  • Chemoprevention / methods
  • Epidermal Cells
  • Epidermis / drug effects*
  • Epidermis / enzymology
  • Epidermis / metabolism
  • Flavonoids / pharmacology*
  • MAP Kinase Signaling System / drug effects*
  • Medicine, Chinese Traditional / methods
  • Mice
  • Mitogen-Activated Protein Kinase 3 / metabolism*
  • Mutation
  • Phosphorylation / drug effects
  • Quercetin / analogs & derivatives
  • Skin Neoplasms / drug therapy
  • Skin Neoplasms / metabolism
  • Skin Neoplasms / prevention & control
  • Transcription Factor AP-1 / antagonists & inhibitors
  • Transcription Factor AP-1 / metabolism
  • Transcriptional Activation / drug effects

Substances

  • Flavonoids
  • Transcription Factor AP-1
  • quercetin 3-O-methyl ether
  • Quercetin
  • Mitogen-Activated Protein Kinase 3