P2-purinergic receptor agonists inhibit the growth of androgen-independent prostate carcinoma cells

J Clin Invest. 1992 Jan;89(1):191-6. doi: 10.1172/JCI115562.

Abstract

To develop a new approach to the treatment of advanced, hormone-refractory prostate cancer, the signal transductions regulating the growth of human androgen-independent prostate carcinoma cell lines were studied. Agonist-stimulated Ca2+ mobilization, a critical regulatory event in other secretory cell types, was studied as a means of identifying previously undescribed plasma membrane receptors that may transduce a growth inhibitory signal. In all of the cell lines tested, P2-purinergic receptor agonists, including ATP and certain hydrolysis-resistant adenine nucleotides, induced a rapid, transient increase in cytoplasmic free Ca2+ that was detectable at 50 to 100 nM ATP, was maximal at 100 microM ATP, and was inhibited approximately 50% by chelation of extracellular Ca2+. Within 8 s after addition, ATP stimulated accumulation of the polyphosphatidylinositol products inositol (1, 4, 5) trisphosphate, inositol (1, 3, 4) trisphosphate, and inositol tetrakisphosphate. In addition to stimulating phosphatidylinositol turnover and Ca2+ mobilization, ATP and hydrolysis-resistant ATP analogues induced greater than 90% inhibition of the growth of all lines tested. These data demonstrate that human androgen-independent prostate carcinoma cells express functional P2-purinergic receptors linked to phospholipase C, and that agonists of this receptor are markedly growth inhibitory, suggesting a novel therapeutic approach to this common adult neoplasm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine Nucleotides / pharmacology
  • Androgens / metabolism*
  • Calcium / metabolism
  • Calcium Channels / metabolism
  • Carcinoma / metabolism*
  • Evaluation Studies as Topic
  • Humans
  • Inositol Phosphates / metabolism
  • Male
  • Phosphatidylinositols / metabolism
  • Prostatic Neoplasms / metabolism*
  • Receptors, Purinergic / metabolism*
  • Signal Transduction / physiology
  • Tumor Cells, Cultured
  • Type C Phospholipases / metabolism

Substances

  • Adenine Nucleotides
  • Androgens
  • Calcium Channels
  • Inositol Phosphates
  • Phosphatidylinositols
  • Receptors, Purinergic
  • Type C Phospholipases
  • Calcium