Growth stimulatory effect of pancreatic spasmolytic polypeptide on cultured colon and breast tumor cells

FEBS Lett. 1989 Apr 24;247(2):303-6. doi: 10.1016/0014-5793(89)81357-2.

Abstract

The effects of a novel polypeptide, pancreatic spasmolytic polypeptide (PSP) on a colon carcinoma cell line (HCT 116) were examined. PSP stimulated the incorporation of [3H]thymidine into HCT 116 cells as well as cell proliferation in a dose-dependent manner. Maximal increase in [3H]thymidine incorporation of 50-60% occurred at 3-300 microM PSP. The VIP-mediated-increase in cAMP levels was reduced by PSP at greater than 1 microM concentrations. PSP is highly homologous to the estrogen-induced pS2 protein in MCF-7 breast cancer cells. We find that PSP also enhanced [3H]thymidine incorporation in MCF-7 cells. These findings indicate for the first time that PSP has growth stimulatory properties.

MeSH terms

  • Animals
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology*
  • Cell Division / drug effects
  • Colonic Neoplasms / metabolism
  • Colonic Neoplasms / pathology*
  • Cyclic AMP / metabolism
  • DNA / biosynthesis
  • Humans
  • Intercellular Signaling Peptides and Proteins
  • Mucins*
  • Muscle Proteins*
  • Neuropeptides*
  • Parasympatholytics
  • Peptides / pharmacology*
  • Swine
  • Trefoil Factor-2
  • Trefoil Factor-3
  • Tumor Cells, Cultured
  • Vasoactive Intestinal Peptide / metabolism
  • Vasoactive Intestinal Peptide / pharmacology

Substances

  • Intercellular Signaling Peptides and Proteins
  • Mucins
  • Muscle Proteins
  • Neuropeptides
  • Parasympatholytics
  • Peptides
  • TFF3 protein, rat
  • Tff2 protein, rat
  • Trefoil Factor-2
  • Trefoil Factor-3
  • Vasoactive Intestinal Peptide
  • pancreatic spasmolytic polypeptide
  • DNA
  • Cyclic AMP