Alterations of anaphase-promoting complex genes in human colon cancer cells

被引:0
作者
Qing Wang
Caroline Moyret-Lalle
Florence Couzon
Christine Surbiguet-Clippe
Jean-Christophe Saurin
Thierry Lorca
Claudine Navarro
Alain Puisieux
机构
[1] Centre d'Oncologie Génétique,
[2] INSERM U453,undefined
[3] Centre Léon Bérard,undefined
[4] 28 rue Laënnec,undefined
[5] Faculté de Pharmacie,undefined
[6] 8 avenue Rockefeller,undefined
[7] Fédération de Spécialitiés Digestives,undefined
[8] Hôpital Edouard Herriot,undefined
[9] Place d'Arsonval,undefined
[10] Centre de Recherches de Biochimie Macromoléculaire,undefined
[11] CNRS UPR 1086,undefined
[12] 1919 route de Mende,undefined
来源
Oncogene | 2003年 / 22卷
关键词
APC/C; cyclosome; ubiquitination; colon cancer; cyclin B1;
D O I
暂无
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学科分类号
摘要
Ubiquitin-mediated proteolysis of cell cycle regulators is a major element of the cell cycle control. The anaphase-promoting complex (APC/C) is a large multisubunit ubiquitin-protein ligase required for the ubiquitination and degradation of G1 and mitotic checkpoint regulators. APC/C-dependent proteolysis regulates cyclin levels in G1, and triggers the separation of sister chromatids at the metaphase–anaphase transition and the destruction of mitotic cyclins at the end of mitosis. Furthermore, it was recently shown that APC/C regulates the degradation of crucial regulators of signal transduction pathways. We report here gene alterations in several components of this complex in human colon cancer cells, including APC6/CDC16 and APC8/CDC23 which are known to be key function elements. The experimental expression of a truncation mutant of APC8/CDC23 subunit (CDC23ΔTPR) leads to abnormal levels of APC/C targets such as cyclin B1 and disturbs the cell cycle progression of colon epithelial cells through mitosis. Overall, these data support the hypothesis of a deleterious role of these mutations during colorectal carcinogenesis.
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页码:1486 / 1490
页数:4
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