Activation of integrin and ceramide signalling pathways can inhibit the mitogenic effect of insulin-like growth factor I (IGF-I) in human breast cancer cell lines

Br J Cancer. 1999 Feb;79(5-6):701-6. doi: 10.1038/sj.bjc.6690113.

Abstract

Cell counting, cell cycle analysis and Western immunoblotting were used to examine the effects of non-apoptotic doses of a ceramide analogue, C2, and a synthetic arginine-glycine-aspartic acid (RGD)-containing peptide, RGD, in MCF-7 and T47D cells to determine whether activation of these signalling pathways could alter the mitogenic potential of insulin-like growth factor I (IGF-I). IGF-I alone increased total cell number in both cell lines, associated with a rise in the percentage of cells in the S-phase of the cell cycle and a co-incident increase in cyclin A production. Treatments alone had no effects on cell number or cyclin A production relative to controls. C2 inhibited IGF-I-induced mitogenesis in both lines, whereas RGD was only effective in the T47D line. Despite inhibition of cell proliferation, IGF-I stimulation of cells in S-phase and of cyclin A levels were unaffected; however, an IGF-I-induced increase in cyclin B1 levels was inhibited by 30%. Low-dose induction of integrin and ceramide signalling pathways causes cells to be blocked in S-phase, thereby inhibiting the normal cycle of events associated with the IGF-I-induced mitotic signal. Activating these pathways may not only restrict tumour growth by induction of apoptosis but they may also directly inhibit IGF-I-induced cell proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms
  • Cell Cycle / drug effects
  • Cell Cycle / physiology
  • Cell Division / drug effects
  • Cyclin A / biosynthesis
  • Cyclin B / biosynthesis
  • Cyclin B1
  • Female
  • Humans
  • Insulin-Like Growth Factor I / antagonists & inhibitors
  • Insulin-Like Growth Factor I / pharmacology*
  • Kinetics
  • Oligopeptides / pharmacology
  • Recombinant Proteins / pharmacology
  • S Phase
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*
  • Sphingosine / analogs & derivatives*
  • Sphingosine / pharmacology
  • Tumor Cells, Cultured

Substances

  • CCNB1 protein, human
  • Cyclin A
  • Cyclin B
  • Cyclin B1
  • N-acetylsphingosine
  • Oligopeptides
  • Recombinant Proteins
  • arginyl-glycyl-glutamic acid
  • Insulin-Like Growth Factor I
  • arginyl-glycyl-aspartic acid
  • Sphingosine