14-3-3 Proteins: Diverse functions in cell proliferation and cancer progression

被引:260
作者
Freeman, Alyson K. [1 ]
Morrison, Deborah K. [1 ]
机构
[1] NCI, Lab Cell & Dev Signaling, Frederick, MD 21702 USA
关键词
14-3-3; Cell proliferation; Cell migration; Actin cytoskeleton; EMT; COFILIN-PHOSPHATASE SLINGSHOT; BREAST-CANCER; MESENCHYMAL TRANSITION; ARGININE METHYLATION; THERAPEUTIC TARGET; ACTIN DYNAMICS; HIPPO PATHWAY; PHOSPHORYLATION; LOCALIZATION; BINDING;
D O I
10.1016/j.semcdb.2011.08.009
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The 14-3-3 proteins were the first phosphoserine/phosphothreonine-binding proteins to be discovered, a finding that provided the foundation for their prominent role in cell signaling. 14-3-3 family members interact with a wide spectrum of proteins including transcription factors, biosynthetic enzymes, cytoskeletal proteins, signaling molecules, apoptosis factors, and tumor suppressors. The interaction with 14-3-3 can have a profound effect on a target protein, altering its localization, stability, conformation, phosphorylation state, activity, and/or molecular interactions. Thus, by modulating the function of a diverse array of binding partners, 14-3-3 proteins have become key regulatory components in many vital cellular processes - processes that are crucial for normal growth and development and that often become dysregulated in human cancer. This review will examine the recent advances that further elucidate the role of 14-3-3 proteins in normal growth and cancer signaling with a particular emphasis on the signaling pathways that impact cell proliferation, cell migration, and epithelial-to-mesenchymal transition. Published by Elsevier Ltd.
引用
收藏
页码:681 / 687
页数:7
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