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. Author manuscript; available in PMC: 2013 Jun 11.
Published in final edited form as: Curr Cancer Drug Targets. 2013 Mar 1;13(3):234–244. doi: 10.2174/1568009611313030002

Figure 1.

Figure 1

Alterations of the AKT pathway in human cancer. Activation of tyrosine kinase receptors through growth factor stimulation or constitutive activation of the receptor through mutation/amplification leads to activation of the AKT signaling pathway. Other mechanisms observed in cancer resulting in AKT signaling include activation of proteins encoded by oncogenes (shown in green) and/or inactivation of tumor suppressors (shown in red). Germline mutations of genes encoding some of these tumor suppressors have been found to be responsible for various hereditary cancer syndromes. AKT-mediated phosphorylation of different downstream proteins converges on signaling pathways important in tumorigenesis, such as cell survival and cell cycle progression (convergence of pathways indicated with a thin, black arrow at the lower part of the figure).