Mechanism of inhibitory effect of P7 on 3T3 cell proliferation induced by basic fibroblast growth factor

 To investigate the mechanism of inhibitory effect of a novel bFGF antagonist peptide isolated from the phage display random heptapeptide library on cell proliferation induced by basic fibroblast growth  factor.  The effect of P7 on cell morphology was observed under an inverted microscope.  Flow cytometry was applied to analyze the effect of P7 on cell cycle progress of bFGF-stimulated cells.  The effect of P7 on bFGF-induced activation of MEK and Erk1/2 in MAPK pathway was detected by Western blotting.  The results showed that no significant cell morphology change was observed in the range of detected concentrations of P7.  Cell cycle analysis showed that P7 decreased S-phase cell population and arrested cell cycle at the G₀/G₁ phase of bFGF-stimulated cells.  The results of MAP kinase activation assay indicated that P7 decreased bFGF-induced MEK and Erk1/2 phosphorylation in a dose-dependent manner.  P7 inhibited proliferation of bFGF-stimulated Balb/c 3T3 cells possibly via cell cycle arrest at the G₀/G₁ phase and down-regulation of signal molecular    activation in MAPK pathway.