1. Priority paper Fibroblast growth factor-2 has opposite effects on human breast cancer MCF-7 cell growth depending on the activation level of the mitogen-activated protein kinase pathway
- Author
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Jean Pierre Caruelle, José Courty, Michel Crépin, Jianfeng Liu, Denis Barritault, Dominique Ledoux, E Chevet, Brigitte Bertin, and Tarik Issad
- Subjects
DNA Replication ,MAPK/ERK pathway ,Chemistry ,Cell growth ,Kinase ,Akt/PKB signaling pathway ,Breast Neoplasms ,Fibroblast growth factor receptor 3 ,Fibroblast growth factor ,Biochemistry ,Cell biology ,Enzyme Activation ,Calcium-Calmodulin-Dependent Protein Kinases ,Cyclic AMP ,Tumor Cells, Cultured ,Humans ,Insulin ,Fibroblast Growth Factor 2 ,Enzyme Inhibitors ,skin and connective tissue diseases ,Protein kinase A ,Protein kinase B - Abstract
In human breast cancer MCF-7 and MCF-7ras cells, we demonstrated that whereas insulin had a mitogenic effect on both cell lines, fibroblast growth factor-2 (FGF-2) had opposite effects, stimulating MCF-7 and inhibiting MCF-7ras cell proliferation. The inhibitory signal induced by FGF-2 was related to sustained mitogen-activated protein kinase (MAPK) activation in MCF-7ras cells, while transient MAPK activation was associated with MCF-7 cell proliferation. FGF-2 was further used in combination with insulin or cAMP. In MCF-7 cells, insulin and cAMP reversed the mitogenic effect of FGF-2. In MCF-7ras cells, insulin did not modify the inhibitory effect of FGF-2, but cAMP markedly enhanced it. These effects were also associated with an increased level and duration of MAPK activation. PD98056 abolished the effect of FGF-2 on DNA synthesis in both cell lines, demonstrating that the dual effect of FGF-2 on cell proliferation is dependent on the activity of the extracellular-signal-regulated kinase 1 and 2 (ERK1/2) signalling pathway.
- Published
- 1998
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