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20191028232223.0 |
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140327s2014 gw | s |||| 0|eng d |
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|a 9783319050263
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|a 10.1007/978-3-319-05026-3
|2 doi
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|a (DE-He213)978-3-319-05026-3
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|a Inuzuka, Hiroyuki.
|e author.
|4 aut
|4 http://id.loc.gov/vocabulary/relators/aut
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| 245 |
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|a SCF and APC E3 Ubiquitin Ligases in Tumorigenesis
|h [electronic resource] /
|c by Hiroyuki Inuzuka, Wenyi Wei.
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| 250 |
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|a 1st ed. 2014.
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| 264 |
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|a Cham :
|b Springer International Publishing :
|b Imprint: Springer,
|c 2014.
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| 300 |
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|a V, 118 p. 11 illus. in color.
|b online resource.
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|a SpringerBriefs in Cancer Research,
|x 2194-1173
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| 490 |
1 |
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|a Springer eBook Collection
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| 505 |
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|a 1. Introduction -- 2. The Fbxw subclass of SCF E3 ubiquitin Ligases -- 3. The FbxL subclass of SCF E3 ubiquitin Ligases -- 4. The Fbxo subclass of SCF E3 ubiquitin Ligases -- 5. APC/Cdc20 and APC/Cdh1 E3 ubiquitin Ligases -- 6. Conclusions and Future Perspectives.
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| 520 |
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|a This SpringerBrief explores the physiological roles of Skp1-Cullin1-F-box Complex (SCF) and Anaphase Promoting Complex (APC) in normal cells and in tumor formation. These two related, multi-subunit E3 ubiquitin ligase enzymes, APC and SCF are thought to be the major driving forces governing proper cell cycle progression. Defective cell cycle regulation leads to genomic instability and ultimately, cancer development. Selective degradation of key cell cycle regulators by the ubiquitin-proteasome system has been proven to be a major regulatory mechanism for ensuring ordered and coordinated cell cycle progression. The SCF and APC E3 ligases have been characterized to play pivotal roles in regulating the cell cycle progression by timely degrading various critical cell cycle regulators. This Brief reviews recent studies that have shown that deregulation of signaling pathways in which the two ubiquitin ligases are involved causes aberrant cell cycle regulation, in turn leading to tumorigenesis. The text also discusses how SCF and APC may present promising therapeutic targets to treat various cancers.
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|a Loaded electronically.
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|a Electronic access restricted to members of the Holy Cross Community.
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|a Cancer research.
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|a Cell cycle.
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|a Proteins .
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