Antagonism between estrogens and androgens on GCDFP-15 gene expression in ZR-75-1 cells and correlation between GCDFP-15 and estrogen as well as progesterone receptor expression in human breast cancer

J Steroid Biochem. 1989;34(1-6):397-402. doi: 10.1016/0022-4731(89)90115-5.

Abstract

The androgen dihydrotestosterone (DHT) caused a maximal 65% inhibition of proliferation of the human breast cancer cells ZR-75-1 after a 10-day incubation period. The same treatment, on the other hand, stimulated by 25-fold the secretion of the breast marker protein GCDFP-15 (gross cystic disease fluid protein-15). The stimulatory effect of DHT on GCDFP-15 mRNA accumulation was already significant (1.6-fold, P less than 0.01) after a 12 h exposure and reached a maximal 25-fold increase after a 12-day incubation period. On the other hand, a 2-day exposure to 1 nM 17 beta-estradiol (E2) alone decreased by 60% GCDFP-15 mRNA levels while it completely blocked the 2.5-fold stimulation of GCDFP-15 secretion induced by concomitant incubation with DHT. Furthermore, a 10-day incubation with E2 increased by 4-fold the proliferation of ZR-75-1 cells whereas such treatment decreased by about 85% both GCDFP-15 mRNA accumulation and the secretion of the glycoprotein. The presence of GCDFP-15 mRNA in human breast cancer samples was restricted to estrogen receptor positive tumors and was significantly correlated with progesterone receptor expression.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Apolipoproteins D
  • Apolipoproteins*
  • Biomarkers, Tumor / analysis
  • Breast Neoplasms
  • Carrier Proteins*
  • Cell Line
  • Dihydrotestosterone / pharmacology*
  • Estradiol / pharmacology*
  • Female
  • Gene Expression / drug effects*
  • Glycoproteins*
  • Humans
  • Kinetics
  • Membrane Transport Proteins*
  • Neoplasm Proteins / genetics*
  • RNA, Messenger / drug effects
  • RNA, Messenger / genetics*
  • Transcription, Genetic / drug effects
  • Tumor Cells, Cultured / drug effects
  • Tumor Cells, Cultured / metabolism*

Substances

  • APOD protein, human
  • Apolipoproteins
  • Apolipoproteins D
  • Biomarkers, Tumor
  • Carrier Proteins
  • Glycoproteins
  • Membrane Transport Proteins
  • Neoplasm Proteins
  • PIP protein, human
  • RNA, Messenger
  • Dihydrotestosterone
  • Estradiol