Epidermal growth factor enhances transcription of human arachidonate 12-lipoxygenase in A431 cells

Biochim Biophys Acta. 1997 Jan 7;1344(1):38-46. doi: 10.1016/s0005-2760(96)00128-2.

Abstract

Epidermal growth factor (EGF), determined by immunoprecipitation and Western blot analysis, increased both enzyme activity and protein level of 12-lipoxygenase in the solubilized microsomes of human epidermoid carcinoma A431 cells, respectively. The EGF-induced expression of 12-lipoxygenase mRNA was inhibited by transcription inhibitors such as actinomycin D and 5,6-dichlorobenzimidazole riboside. Promoters of different lengths for human 12-lipoxygenase gene were used to prepare the luciferase fusion vectors. These construct plasmids were transiently transfected into A431 cells, and the induction of luciferase expression by EGF was examined. A 4- to 6-fold increase in luciferase reporter activity stimulated by EGF for 18 h treatment was observed in plasmids with the 5'-flanking region length of -951 bp and that of -224 bp upstream from translation starting site. The time-dependent induction of luciferase activity by EGF paralleled the EGF-induced enzyme activity and expression of 12-lipoxygenase protein. Taken together, the results of this study indicate that EGF enhanced the transcription of the human 12-lipoxygenase gene, resulting in an increase in the amount and activity of 12-lipoxygenase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arachidonate 12-Lipoxygenase / genetics
  • Arachidonate 12-Lipoxygenase / metabolism*
  • Carcinoma, Squamous Cell / metabolism
  • Cytosol / enzymology
  • Dactinomycin / pharmacology
  • Dichlororibofuranosylbenzimidazole / pharmacology
  • Enzyme Activation / drug effects
  • Epidermal Growth Factor / pharmacology*
  • Gene Expression Regulation / genetics
  • Genes, Reporter / genetics
  • Humans
  • Luciferases / genetics
  • Luciferases / metabolism
  • Microsomes / enzymology
  • Nucleic Acid Synthesis Inhibitors / pharmacology
  • Promoter Regions, Genetic / genetics
  • RNA, Messenger / metabolism
  • Transcription, Genetic / drug effects*
  • Transcription, Genetic / genetics
  • Transfection / genetics
  • Tumor Cells, Cultured
  • beta-Galactosidase / genetics
  • beta-Galactosidase / metabolism

Substances

  • Nucleic Acid Synthesis Inhibitors
  • RNA, Messenger
  • Dactinomycin
  • Dichlororibofuranosylbenzimidazole
  • Epidermal Growth Factor
  • Arachidonate 12-Lipoxygenase
  • Luciferases
  • beta-Galactosidase