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Regulation of Skp2 Expression and Activity and Its Role in Cancer Progression
Author(s) -
ChiaHsin Chan,
Szu-Wei Lee,
Jing Wang,
Hui-Kuan Lin
Publication year - 2010
Publication title -
the scientific world journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.453
H-Index - 93
eISSN - 2356-6140
pISSN - 1537-744X
DOI - 10.1100/tsw.2010.89
Subject(s) - skp2 , ubiquitin ligase , carcinogenesis , cancer research , biology , cell cycle , ubiquitin , cancer , cell cycle progression , f box protein , phosphorylation , cell growth , microbiology and biotechnology , skp1 , genetics , gene
The regulation of cell cycle entry is critical for cell proliferation and tumorigenesis. One of the key players regulating cell cycle progression is the F-box protein Skp2. Skp2 forms a SCF complex with Skp1, Cul-1, and Rbx1 to constitute E3 ligase through its F-box domain. Skp2 protein levels are regulated during the cell cycle, and recent studies reveal that Skp2 stability, subcellular localization, and activity are regulated by its phosphorylation. Overexpression of Skp2 is associated with a variety of human cancers, indicating that Skp2 may contribute to the development of human cancers. The notion is supported by various genetic mouse models that demonstrate an oncogenic activity of Skp2 and its requirement in cancer progression, suggesting that Skp2 may be a novel and attractive therapeutic target for cancers.

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