14-3-3 proteins as signaling integration points for cell cycle control and apoptosis.

Title14-3-3 proteins as signaling integration points for cell cycle control and apoptosis.
Publication TypeJournal Article
Year of Publication2011
AuthorsGardino, AK, Yaffe, MB
JournalSemin Cell Dev Biol
Volume22
Issue7
Pagination688-95
Date Published2011 Sep
ISSN1096-3634
Keywords14-3-3 Proteins, Animals, Apoptosis, Cell Cycle, Cell Cycle Checkpoints, DNA Damage, DNA Repair, Humans, Mitosis, Protein Binding, Protein Kinases, Signal Transduction
Abstract

14-3-3 proteins play critical roles in the regulation of cell fate through phospho-dependent binding to a large number of intracellular proteins that are targeted by various classes of protein kinases. 14-3-3 proteins play particularly important roles in coordinating progression of cells through the cell cycle, regulating their response to DNA damage, and influencing life-death decisions following internal injury or external cytokine-mediated cues. This review focuses on 14-3-3-dependent pathways that control cell cycle arrest and recovery, and the influence of 14-3-3 on the apoptotic machinery at multiple levels of regulation. Recognition of 14-3-3 proteins as signaling integrators that connect protein kinase signaling pathways to resulting cellular phenotypes, and their exquisite control through feedforward and feedback loops, identifies new drug targets for human disease, and highlights the emerging importance of using systems-based approaches to understand signal transduction events at the network biology level.

DOI10.1016/j.semcdb.2011.09.008
Alternate JournalSemin. Cell Dev. Biol.
PubMed ID21945648
PubMed Central IDPMC3507455
Grant ListCA-112967 / CA / NCI NIH HHS / United States
ES-015339 / ES / NIEHS NIH HHS / United States
GM-60594 / GM / NIGMS NIH HHS / United States
GM-68762 / GM / NIGMS NIH HHS / United States
P50 GM068762-10 / GM / NIGMS NIH HHS / United States
R01 ES015339-05 / ES / NIEHS NIH HHS / United States
R01 GM060594-09 / GM / NIGMS NIH HHS / United States
U54 CA112967-08 / CA / NCI NIH HHS / United States