CDK inhibitors: cell cycle regulators and beyond

Dev Cell. 2008 Feb;14(2):159-69. doi: 10.1016/j.devcel.2008.01.013.

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Apoptosis
  • Cell Cycle*
  • Cyclin-Dependent Kinase Inhibitor Proteins / metabolism*
  • Cytoskeleton / metabolism
  • Gene Expression Regulation
  • Humans
  • Tumor Suppressor Proteins / metabolism

Substances

  • Cyclin-Dependent Kinase Inhibitor Proteins
  • Tumor Suppressor Proteins