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- Title
p27(kip1) functional regulation in human cancer: a potential target for therapeutic designs.
- Authors
Belletti, B; Nicoloso, M S; Schiappacassi, M; Chimienti, E; Berton, S; Lovat, F; Colombatti, A; Baldassarre, G
- Abstract
The mitotic cell cycle is a tightly regulated process that ensures the correct division of one cell into two daughter cells. Progress along the different phases of the cell cycle is positively regulated by the sequential activation of a family of serine-threonine kinases called CDKs (Cyclin Dependent Kinases). Their activity is counteracted by small proteins known as CDK inhibitors (CKI) that ensure the correct timing of CDK activation in the different phases of the cell cycle. The present review will deal with the role of one of this CKI, p27(kip1), in human cancer, focusing in particular on the mechanisms underlying its functional inactivation in tumor cells. p27(kip1) protein downregulation is usually achieved by proteasomal degradation and is often correlated to a worse prognosis in several types of human cancers, resulting in the reduction of disease free and overall survival. More recently, it has been proposed that p27(kip1) protein, rather than degraded, can be functionally inactivated. The mechanisms and the implications of these two types of p27(kip1) deregulation will be discussed and some potential therapeutic approaches targeting p27(kip1) functions will be proposed.
- Publication
Current medicinal chemistry, 2005, Vol 12, Issue 14, p1589
- ISSN
0929-8673
- Publication type
Journal Article
- DOI
10.2174/0929867054367149