14-3-3 proteins as potential therapeutic targets |
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Authors: | Zhao Jing Meyerkord Cheryl L Du Yuhong Khuri Fadlo R Fu Haian |
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Affiliation: | aDepartment of Pharmacology, Emory University School of Medicine, Atlanta, GA 30322, USA;bDepartment of Biochemistry and Molecular Biology, the Fourth Military Medical University, Xi’an 710032, China;cDepartment of Hematology & Medical Oncology, Emory University School of Medicine, Atlanta, GA 30322, USA;dEmory Chemical Biology Discovery Center, Emory University School of Medicine, Atlanta, GA 30322, USA |
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Abstract: | The 14-3-3 family of phosphoserine/phosphothreonine-binding proteins dynamically regulates the activity of client proteins in various signaling pathways that control diverse physiological and pathological processes. In response to environmental cues, 14-3-3 proteins orchestrate the highly regulated flow of signals through complex networks of molecular interactions to achieve well-controlled physiological outputs, such as cell proliferation or differentiation. Accumulating evidence now supports the concept that either an abnormal state of 14-3-3 protein expression, or dysregulation of 14-3-3/client protein interactions, contributes to the development of a large number of human diseases. In particular, clinical investigations in the field of oncology have demonstrated a correlation between upregulated 14-3-3 levels and poor survival of cancer patients. These studies highlight the rapid emergence of 14-3-3 proteins as a novel class of molecular target for potential therapeutic intervention. The current status of 14-3-3 modulator discovery is discussed. |
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Keywords: | 14-3-3 inhibitor Stabilizer |
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