Attenuation of c-Jun and Sp1 expression and p300 recruitment to gene promoter confers the trichostatin A-induced inhibition of 12(S)-lipoxygenase expression in EGF-treated A431 cells

Eur J Pharmacol. 2008 Sep 4;591(1-3):36-42. doi: 10.1016/j.ejphar.2008.06.041. Epub 2008 Jun 15.

Abstract

The mechanism by which the histone deacetylase (HDAC) inhibitor trichostatin A inhibits epidermal growth factor (EGF)-induced human 12(S)-lipoxygenase expression was studied. Trichostatin A treatment of human epidermoid carcinoma A431 cells inhibited the EGF-induced 12(S)-lipoxygenase enzymatic activity in a dose-dependent manner that was consistent with the expression of 12(S)-lipoxygenase mRNA and protein. Confocal microscopy indicated that trichostatin A treatment of cells resulted in downregulation of EGF-induced c-Jun expression. Western blotting revealed that trichostatin A treatment of cells resulted in downregulation of EGF-induced c-Jun and constitutively Sp1 expression. Results of a chromatin immunoprecipitation assay revealed that trichostatin A treatment of cells also upregulated Sp1 acetylation and attenuated the recruitment of Sp1, c-Jun, and p300 to the 12(S)-lipoxygenase gene promoter. These results suggested that trichostatin A inhibited EGF-induced 12(S)-lipoxygenase expression by multiple mechanisms, including the attenuation of c-Jun and Sp1 expression and p300 recruitment to the 12(S)-lipoxygenase gene promoter.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arachidonate 12-Lipoxygenase / drug effects*
  • Arachidonate 12-Lipoxygenase / metabolism
  • Blotting, Western
  • Cell Line, Tumor
  • Chromatin Immunoprecipitation
  • Dose-Response Relationship, Drug
  • E1A-Associated p300 Protein / drug effects
  • E1A-Associated p300 Protein / metabolism
  • Enzyme Inhibitors / administration & dosage
  • Enzyme Inhibitors / pharmacology*
  • Epidermal Growth Factor / pharmacology
  • Gene Expression Regulation / drug effects
  • Humans
  • Hydroxamic Acids / administration & dosage
  • Hydroxamic Acids / pharmacology*
  • Promoter Regions, Genetic / drug effects
  • Proto-Oncogene Proteins c-jun / drug effects
  • Proto-Oncogene Proteins c-jun / metabolism*
  • RNA, Messenger / drug effects
  • RNA, Messenger / metabolism
  • Sp1 Transcription Factor / drug effects
  • Sp1 Transcription Factor / metabolism

Substances

  • Enzyme Inhibitors
  • Hydroxamic Acids
  • Proto-Oncogene Proteins c-jun
  • RNA, Messenger
  • Sp1 Transcription Factor
  • trichostatin A
  • Epidermal Growth Factor
  • Arachidonate 12-Lipoxygenase
  • E1A-Associated p300 Protein
  • EP300 protein, human