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

被引:817
作者
Chu, Isabel M. [1 ,2 ]
Hengst, Ludger [3 ]
Slingerland, Joyce M. [1 ,2 ]
机构
[1] Univ Miami, Miller Sch Med, Braman Family Breast Canc Inst, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, Dept Biochem & Mol Biol, Miami, FL 33136 USA
[3] Innsbruck Med Univ, Bioctr, Div Med Chem, A-6020 Innsbruck, Austria
关键词
D O I
10.1038/nrc2347
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
sThe 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.
引用
收藏
页码:253 / 267
页数:15
相关论文
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