Induction of Mdm2 and enhancement of cell survival by bFGF

Eitan Shaulian, Dalia Resnitzky, Ohad Shifman, Giovanni Blandino, Abraham Amsterdam, Avner Yayon, Moshe Oren*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

98 Scopus citations


Basic fibroblast growth factor (bFGF) can exert mitogenic and viability-promoting effects in a wide range of biological systems. The biochemical activities mediating the cell survival function of bFGF are largely unknown. We report here that exposure of fibroblasts to bFGF, which confers upon them increased survival, also causes at the same time an increase in cellular levels of the Mdm2 oncoprotein. Cells constitutively exposed to a bFGF autocrine loop are more refractory to killing by cisplatin. This increased chemoresistance coincides with elevated Mdm2 and reduced activation of the endogenous p53, resulting in inefficient transcriptional activation of the bax gene promoter. Importantly, unlike Mdm2 accumulation in fibroblasts exposed to DNA damage, induction of Mdm2 by bFGF does not occur through a p53-mediated pathway. The role of p53 in DNA damage-induced apoptosis and the ability of Mdm2 to block p53-mediated cell death are well established. These findings therefore suggest that induction of Mdm2 and the subsequent inhibition of p53 function may contribute, at least partially, to the anti-apoptotic effects of bFGF and possibly some other survival factors.

Original languageAmerican English
Pages (from-to)2717-2725
Number of pages9
Issue number22
StatePublished - 1997
Externally publishedYes

Bibliographical note

Funding Information:
The help of D Aharoni and D Hecht is gratefully acknowledged. We thank A Levine and A Teresky for the gift of (10)1 cells. This work was supported in part by PHS grant RO1 CA 40099 from the National Cancer Institute, and by grants from the Israel-USA Binational Science Foundation and the Leo and Julia Forchheimer Center for Molecular Genetics.


  • Apoptosis
  • Cisplatin
  • Mdm2
  • bFGF
  • p53


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