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PMID: 18354415 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

The Cdk inhibitor p27 in human cancer: prognostic potential and relevance to anticancer therapy.

Nature reviews. Cancer ·Vol. 8 ·No. 4 ·2008-04-00 ·Pages 253-67

Chu IM, Hengst L, Slingerland JM

Abstract

The cyclin-dependent kinase (Cdk) inhibitor p27 (also known as KIP1) regulates cell proliferation, cell motility and apoptosis. Interestingly, the protein can exert both positive and negative functions on these processes. Diverse post-translational modifications determine the physiological role of p27. Phosphorylation regulates p27 binding to and inhibition of cyclin-Cdk complexes, its localization and its ubiquitin-mediated proteolysis. In cancers, p27 is inactivated through impaired synthesis, accelerated degradation and by mislocalization. Moreover, studies in several tumour types indicate that p27 expression levels have both prognostic and therapeutic implications.

MeSH Terms
Antineoplastic Agents/therapeutic use Cyclin-Dependent Kinase Inhibitor p27/genetics,metabolism Humans Neoplasms/drug therapy,metabolism Phosphorylation Prognosis
Chemicals
Antineoplastic Agents Cyclin-Dependent Kinase Inhibitor p27
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Chu Isabel M
Braman Family Breast Cancer Institute, and Department of Biochemistry and Molecular Biology, University of Miami Miller School of Medicine, 1580 NW 10th Avenue, Miami, Florida 33136, USA.
Hengst Ludger
Slingerland Joyce M
Article Info
Journal
Nature reviews. Cancer
Abbr.
Nat Rev Cancer
ISSN
1474-1768
Published
2008-04-00
Pages
253-67
Language
English
Region
England
NLM ID
101124168
Subset
IM
Grants
NCI NIH HHS · 1R01CA105118-01 · United States
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