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Ferritin expression modulates cell cycle dynamics and cell responsiveness to H-ras-induced growth via expansion of
Or Kakhlon1, Yosef Gruenbaum, Z Ioav Cabantchik
1Department of Biological Chemistry, Institute of Life Sciences, Hebrew University, Jerusalem, 91904, Israel.
Abstract:
Repression or overexpression of ferritin accelerated or retarded cell cycling respectively, via changes in the cellular labile iron pool (LIP). A rise in LIP is caused by ferritin repression enhanced growth, induced by H-ras, and reverted growth arrest is induced by dominant negative H-ras. The studies indicate that repression of ferritin expression provides a mechanism by which certain oncogenes lead to cell growth stimulation.
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