Consequences of CK2 signaling to the nuclear matrix

S. Yu, H. Wang, A. Davis, K. Ahmed

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

Protein kinase CK2 is recognized as one of the key cellular signals for cell growth and proliferation. Its nuclear targeting appears to be critical to its role in these functions. In the nucleus, nuclear matrix (NM) which plays a major role in growth-related activities is a primary locus for CK2 signaling. A variety of growth stimuli evoke a rapid translocation of the CK2 to the NM whereas removal of these factors has the opposite effect. These studies, employing various experimental models of cell growth (involving different growth-stimulatory factors), have suggested that rapid shuttling of CK2 to the NM is a key feature of early growth control. By contrast, removal of growth-stimulatory factors leading to the loss of cell viability is associated with early loss of CK2 from the NM (and chromatin). This indicates that absence of CK2 from the nuclear compartment is contributory to induction of cell death via apoptosis, implying a protective role for CK2 against cell death. Here, we review the evidence that suggests that CK2 signaling in the NM is not only involved in cell growth but also in cell survival.

Original languageEnglish (US)
Pages (from-to)67-71
Number of pages5
JournalMolecular and cellular biochemistry
Volume227
Issue number1-2
DOIs
StatePublished - 2001

Bibliographical note

Funding Information:
This work was supported in part by United States Public Health Service Research Grant CA-15062 awarded by the National Cancer Institute, Department of Health and Human Services, and in part by the Medical Research Fund of the United States Department of Veterans Affairs.

Keywords

  • Adaptive response
  • Apoptosis
  • Cell growth
  • Cell survival
  • Nuclear matrix
  • Protein kinase CK2

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