The ubiquitin-proteasome system in glioma cell cycle control
dc.creator | Vlachostergios, P. J. | en |
dc.creator | Voutsadakis, I. A. | en |
dc.creator | Papandreou, C. N. | en |
dc.date.accessioned | 2015-11-23T10:53:48Z | |
dc.date.available | 2015-11-23T10:53:48Z | |
dc.date.issued | 2012 | |
dc.identifier | 10.1186/1747-1028-7-18 | |
dc.identifier.issn | 1747-1028 | |
dc.identifier.uri | http://hdl.handle.net/11615/34535 | |
dc.description.abstract | A major determinant of cell fate is regulation of cell cycle. Tight regulation of this process is lost during the course of development and progression of various tumors. The ubiquitin-proteasome system (UPS) constitutes a universal protein degradation pathway, essential for the consistent recycling of a plethora of proteins with distinct structural and functional roles within the cell, including cell cycle regulation. High grade tumors, such as glioblastomas have an inherent potential of escaping cell cycle control mechanisms and are often refractory to conventional treatment. Here, we review the association of UPS with several UPS-targeted proteins and pathways involved in regulation of the cell cycle in malignant gliomas, and discuss the potential role of UPS inhibitors in reinstitution of cell cycle control. | en |
dc.source | Cell Division | en |
dc.source.uri | <Go to ISI>://WOS:000309980800001 | |
dc.subject | Ubiquitin-proteasome system | en |
dc.subject | Glioma | en |
dc.subject | Proteasome inhibitors | en |
dc.subject | Ubiquitin | en |
dc.subject | Cell cycle | en |
dc.subject | GROWTH IN-VITRO | en |
dc.subject | TUMOR-SUPPRESSOR | en |
dc.subject | DOWN-REGULATION | en |
dc.subject | THERAPEUTIC | en |
dc.subject | IMPLICATIONS | en |
dc.subject | RETINOBLASTOMA PROTEIN | en |
dc.subject | DEPENDENT DEGRADATION | en |
dc.subject | GLIOBLASTOMA CELLS | en |
dc.subject | MALIGNANT GLIOMAS | en |
dc.subject | P53 PROTEIN | en |
dc.subject | PATHWAY | en |
dc.subject | Cell Biology | en |
dc.title | The ubiquitin-proteasome system in glioma cell cycle control | en |
dc.type | journalArticle | en |
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