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Phosphorylation and Regulation of Raf by Akt (Protein Kinase B)
1.1K
Citations
20
References
1999
Year
Cell DeathCancer BiologyTumor BiologySignaling PathwayCell RegulationReceptor Tyrosine KinaseProtein Kinase RafCell SignalingCancer ResearchProtein Kinase BMolecular PhysiologyBiochemistryCell Cycle ArrestGene ExpressionCell BiologyProtein PhosphorylationSignal TransductionNatural SciencesProtein KinaseBreast CancerTumor SuppressorCellular BiochemistrySystems BiologyMedicine
Activation of the protein kinase Raf can lead to opposing cellular responses such as proliferation, growth arrest, apoptosis, or differentiation. Akt (protein kinase B), a member of a different signaling pathway that also regulates these responses, interacted with Raf and phosphorylated this protein at a highly conserved serine residue in its regulatory domain in vivo. This phosphorylation of Raf by Akt inhibited activation of the Raf-MEK-ERK signaling pathway and shifted the cellular response in a human breast cancer cell line from cell cycle arrest to proliferation. These observations provide a molecular basis for cross talk between two signaling pathways at the level of Raf and Akt.
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