Estrogen induces c-Ha-ras expression via activation of tyrosine kinase in uterine endometrial fibroblasts and cancer cells

J Steroid Biochem Mol Biol. 1995 Oct;55(1):25-33. doi: 10.1016/0960-0760(95)00145-p.

Abstract

Endometrial fibroblasts derived from uterine endometrium as controls and endometrial cancer cells (Ishikawa and HHUA cells) were used to analyze the manner of induction of c-Ha-ras transcripts in endometrial cancers, some of which are estrogen-dependent in growth. Estrogen increased c-Ha-ras expression and tyrosine kinase (TK) activity in fibroblast and Ishikawa cells, but not in HHUA cells. Progesterone diminished c-Ha-ras expression and tyrosine kinase (TK) activity induced by estradiol in the fibroblasts, but not in Ishikawa cells, which persistently overexpressed c-Ha-ras. In these cells, epidermal growth factor (EGF) increased c-Ha-ras expression as did estradiol. Pretreatment with tyrphostin, an inhibitor of TK, abolished estrogen-inducible overexpression of c-Ha-ras. The combination of both estradiol and EGF at maximum effective concentration exerted no additive or synergistic effect on induction of c-Ha-ras expression. In conclusion, persistent activation of TK might lead to overexpression of c-Ha-ras in some endometrial cancer cells under estrogen predominant milieu, which might be associated with the transformation or growth potential.

MeSH terms

  • Adenocarcinoma / enzymology
  • Adenocarcinoma / genetics
  • Adult
  • Base Sequence
  • Carcinoma / enzymology
  • Carcinoma / genetics
  • Endometrial Neoplasms / enzymology
  • Endometrial Neoplasms / genetics*
  • Endometrium / cytology
  • Endometrium / drug effects
  • Enzyme Activation
  • Enzyme Inhibitors / pharmacology
  • Epidermal Growth Factor / pharmacology
  • Estradiol / pharmacology*
  • Female
  • Fibroblasts / drug effects
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation, Neoplastic / drug effects*
  • Humans
  • Molecular Sequence Data
  • Progesterone / pharmacology
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Protein-Tyrosine Kinases / metabolism*
  • Proto-Oncogene Proteins p21(ras) / genetics*
  • RNA, Messenger / biosynthesis
  • Tumor Cells, Cultured

Substances

  • Enzyme Inhibitors
  • RNA, Messenger
  • Progesterone
  • Estradiol
  • Epidermal Growth Factor
  • Protein-Tyrosine Kinases
  • HRAS protein, human
  • Proto-Oncogene Proteins p21(ras)