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      CDK inhibitors: cell cycle regulators and beyond.

      Developmental Cell
      Animals, Apoptosis, Cell Cycle, Cyclin-Dependent Kinase Inhibitor Proteins, metabolism, Cytoskeleton, Gene Expression Regulation, Humans, Tumor Suppressor Proteins

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          Abstract

          First identified as cell cycle inhibitors mediating the growth inhibitory cues of upstream signaling pathways, the cyclin-CDK inhibitors of the Cip/Kip family p21Cip1, p27Kip1, and p57Kip2 have emerged as multifaceted proteins with functions beyond cell cycle regulation. In addition to regulating the cell cycle, Cip/Kip proteins play important roles in apoptosis, transcriptional regulation, cell fate determination, cell migration and cytoskeletal dynamics. A complex phosphorylation network modulates Cip/Kip protein functions by altering their subcellular localization, protein-protein interactions, and stability. These functions are essential for the maintenance of normal cell and tissue homeostasis, in processes ranging from embryonic development to tumor suppression.

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          Author and article information

          Journal
          18267085
          10.1016/j.devcel.2008.01.013

          Chemistry
          Animals,Apoptosis,Cell Cycle,Cyclin-Dependent Kinase Inhibitor Proteins,metabolism,Cytoskeleton,Gene Expression Regulation,Humans,Tumor Suppressor Proteins

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