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PMID: 12479224 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

The role of the cyclin-dependent kinase inhibitor p21 in apoptosis.

Molecular cancer therapeutics ·Vol. 1 ·No. 8 ·2002-06-00 ·Pages 639-49

Gartel AL, Tyner AL

Abstract

Cancer develops when the balance between cell proliferation and cell death is disrupted, and the ensuing aberrant proliferation leads to tumor growth. The cyclin-dependent kinase inhibitor p21 is induced by both p53-dependent and -independent mechanisms following stress, and induction of p21 may cause cell cycle arrest. As a proliferation inhibitor, p21 is poised to play an important role in preventing tumor development. This notion is supported by data indicating that p21-null mice are more prone to spontaneous and induced tumorigenesis, and p21 synergizes with other tumor suppressors to protect against tumor progression in mice. However, a number of recent studies have pointed out that in addition to being an inhibitor of cell proliferation, p21 acts as an inhibitor of apoptosis in a number of systems, and this may counteract its tumor-suppressive functions as a growth inhibitor. In the current review, we discuss the role of p21 in regulating cell death and the potential relevance of its expression in cancer.

MeSH Terms
Animals Apoptosis Cell Death Cyclin-Dependent Kinase Inhibitor p21 Cyclins/physiology Humans Mice Models, Biological Neoplasms/pathology Tumor Suppressor Protein p53/metabolism
Chemicals
CDKN1A protein, human Cdkn1a protein, mouse Cyclin-Dependent Kinase Inhibitor p21 Cyclins Tumor Suppressor Protein p53
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Gartel Andrei L
Department of Molecular Genetics, University of Illinois College of Medicine, Chicago, Illinois 60607, USA. [email protected]
Tyner Angela L
Article Info
Journal
Molecular cancer therapeutics
Abbr.
Mol Cancer Ther
ISSN
1535-7163
Published
2002-06-00
Pages
639-49
Language
English
Region
United States
NLM ID
101132535
Subset
IM
Grants
NIDDK NIH HHS · R01 DK056283 · United States
NIDDK NIH HHS · R01 DK056283-05 · United States
NIDDK NIH HHS · R01 DK56283 · United States
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