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 The p53 orchestra: Mdm2 and Mdmx set the tone Wade M; Wang YV; Wahl GMTrends Cell Biol  2010[May]; 20 (5): 299-309The activities of p53 cover diverse aspects of cell biology, including cell cycle  control, apoptosis, metabolism, fertility, differentiation and cellular  reprogramming. Although loss of p53 function engenders tumor susceptibility,  hyperactivation of p53 is lethal. Therefore, p53 activity must be strictly  regulated to maintain normal tissue homeostasis. Critical for the control of p53  function are its two main negative regulators: Mdm2 and Mdmx. Recent reports have  provided insight into the complex mechanisms that regulate these two proteins and  have revealed novel functions for each. Here, we review and evaluate models of  Mdm2- and Mdmx-dependent regulation of p53 activity. Both Mdm2 and Mdmx receive  input from numerous signaling pathways and interact with many proteins in  addition to p53. Therefore, we also consider roles for Mdm2 and Mdmx in  additional cancer-related networks, including Notch signaling and the  epithelial-to-mesenchymal transition.|Animals[MESH]|Cell Cycle Proteins[MESH]|Humans[MESH]|Models, Biological[MESH]|Nuclear Proteins/genetics/*metabolism[MESH]|Phosphorylation[MESH]|Protein Processing, Post-Translational[MESH]|Proto-Oncogene Proteins c-mdm2/genetics/*metabolism[MESH]|Proto-Oncogene Proteins/genetics/*metabolism[MESH]|Tumor Suppressor Protein p53/genetics/*metabolism[MESH]|Ubiquitination[MESH]
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