Accession Number : ADA470865


Title :   The Role of Ubiquitin E3 Ligase SCF-SKP2 in Prostate Cancer Development


Descriptive Note : Final rept. 19 Jan 2004-18 Jan 2007


Corporate Author : YALE UNIV NEW HAVEN CT SCHOOL OF MEDICINE


Personal Author(s) : Zhang, Hui


Full Text : https://apps.dtic.mil/dtic/tr/fulltext/u2/a470865.pdf


Report Date : Feb 2007


Pagination or Media Count : 41


Abstract : Low or absent expression of CDK inhibitor p27Kip1 is associated with malignant prostatecarcinomas. Loss of tumor suppressors p53 and Pten is also associated with prostate cancers. We found that p27 is regulated by both SCF-SKP2 and a novel ubiquitin E3 ligase containing CUL4-DDB1-WD40-repeat proteins. In addition, we have identified that a specific CUL4A-DDB1-L2DTL/CDT2-PCNA ubiquitin E3 ligase binds and targets p53 polyubiquitination- dependentproteolysis in cooperation with MDM2. By interacting with a WD40-repeat proteins as asubstrate targeting subunit, the CUL4-DDB1 ubiquitin E3 ligase regulates a wide array of biological events including cell cycle regulation, genome stability, and histone methylation;alteration of these events have been shown to associate with the development of prostatecarcinogenesis. We in addition found that expression of SKP2 and Pten heterozygosity do notcooperate in the mouse prostate carcinoma models, suggesting that SKP2 may act downstream ofPten pathway. Our work provides novel insights into the mechanism of prostate tumorigenesis.


Descriptors :   *HISTONES , *PROSTATE CANCER , CONTROL , PRODUCTION , BIOLOGY , MODELS , GENOME , NEOPLASMS , CYCLES , PROSTATE GLAND , METHYLATION


Subject Categories : Medicine and Medical Research


Distribution Statement : APPROVED FOR PUBLIC RELEASE