SUMOylation in carcinogenesis

被引:130
作者
Bettermann, Kira [1 ]
Benesch, Martin [2 ]
Weis, Serge [3 ]
Haybaeck, Johannes [1 ]
机构
[1] Med Univ Graz, Inst Pathol, A-8036 Graz, Austria
[2] Med Univ Graz, Div Pediat Hematol & Oncol, Dept Pediat & Adolescent Med, A-8036 Graz, Austria
[3] State Neuropsychiat Hosp Wagner Jauregg, Neuropathol Lab, Dept Pathol & Neuropathol, Linz, Austria
关键词
SUMO; Cancer; Ubiquitin; SUMO-SPECIFIC PROTEASE; NF-KAPPA-B; NUCLEAR-PORE COMPLEX; HISTONE DEACETYLASE INHIBITORS; CHROMATIN-REMODELING COMPLEX; CONJUGATING ENZYME UBC9; AXIN-BINDING PROTEIN; TRANSCRIPTION FACTOR; ANDROGEN RECEPTOR; E3; LIGASE;
D O I
10.1016/j.canlet.2011.10.036
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
SUMOylation is a post-translational modification characterized by covalent and reversible binding of small ubiquitin-like modifier (SUMO) to a target protein. In mammals, four different isoforms, termed SUMO-1, -2, -3 and -4 have been identified so far. SUMO proteins are critically involved in the modulation of nuclear organization and cell viability. Their expression is significantly increased in processes associated with carcinogenesis such as cell growth, differentiation, senescence, oxidative stress and apoptosis. Little is known about the role of SUMOylation in cancer development. Therefore the present review focuses on possible implications of SUMOylation in carcinogenesis highlighting its impact as an important regulatory cell cycle protein. Moreover, novel opportunities for therapeutic approaches are discussed. The differential expression levels, the target protein preferences and the function of the SUMO pathway in different cancer subtypes raises unexpected issues questioning our understanding of the implication of SUMO in carcinogenesis. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:113 / 125
页数:13
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