Differential effects of phorbol esters on c-fos and c-myc and ornithine decarboxylase gene expression in mouse skin in vivo

Carcinogenesis. 1988 May;9(5):831-5. doi: 10.1093/carcin/9.5.831.

Abstract

Hyperplasiogenic and tumor-promoting phorbol esters such as 12-O-tetradecanoylphorbol-13-acetate or 12-O-retinoylphorbol-13-acetate induce the sequential transient expression of the proto-oncogenes c-fos and c-myc and the ornithine decarboxylase gene in mouse skin in vivo. This sequence of biochemical events probably depends on an activation of protein kinase C by these agents. The non-irritant skin mitogens 4-O-methyl-12-O-tetradecanoylphorbol-13-acetate and ethyl phenyl propiolate do not increase the expression of these genes to a comparable extent. Thus, 12-O-tetradecanoylphorbol-13-acetate and 12-O-retinoylphorbol-13-acetate induce epidermal hyperproliferation by different biochemical mechanisms as do 4-O-methyl-12-O-tetradecanoylphorbol-13-acetate and ethylphenylpropiolate.

MeSH terms

  • Animals
  • Female
  • Hyperplasia
  • Mice
  • Ornithine Decarboxylase / genetics*
  • Phorbol Esters / toxicity*
  • Proto-Oncogenes*
  • RNA, Messenger / analysis
  • Skin / drug effects*
  • Skin / metabolism
  • Skin / pathology
  • Tetradecanoylphorbol Acetate / toxicity

Substances

  • Phorbol Esters
  • RNA, Messenger
  • 12-O-retinoylphorbol-13-acetate
  • Ornithine Decarboxylase
  • Tetradecanoylphorbol Acetate