Reduced NGF secretion by HT-29 human colon cancer cells treated with a GRPR antagonist

Protein Pept Lett. 2009;16(6):650-2. doi: 10.2174/092986609788490177.

Abstract

The gastrin-releasing peptide receptor (GRPR) is a therapeutic target in colon cancer. Here we show that the GRPR antagonist RC-3095 (10(-3), 10(-6), or 1 microM) decreases nerve growth factor (NGF) secretion measured by enzyme-linked immunosorbent assay (ELISA) in HT-29 human colon carcinoma cells. The results suggest that decreased secretion of neurotrophins might be a novel mechanism by which GRPR antagonists exert their antiproliferative effects in cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Bombesin / analogs & derivatives*
  • Bombesin / pharmacology
  • Dose-Response Relationship, Drug
  • Enzyme-Linked Immunosorbent Assay
  • HT29 Cells
  • Humans
  • Nerve Growth Factor / metabolism*
  • Peptide Fragments / pharmacology*
  • Receptors, Bombesin / antagonists & inhibitors*

Substances

  • NGF protein, human
  • Peptide Fragments
  • Receptors, Bombesin
  • bombesin (6-14), Tpi(6)-Leu(13)-psi(CH2NH)-Leu(14)-
  • Nerve Growth Factor
  • Bombesin