Developing Practical Therapeutic Strategies that Target Protein SUMOylation

被引:7
|
作者
Cox, Olivia F. [1 ]
Huber, Paul W. [1 ]
机构
[1] Univ Notre Dame, Ctr Stem Cells & Regenerat Med, Harper Canc Res Inst, Dept Chem & Biochem, Notre Dame, IN 46556 USA
基金
美国国家卫生研究院;
关键词
SUMO; SUMO ligase; SENP protease; heart development; heart failure; cancer; neurodegenerative disease; congenital birth defects; spina bifida; neural tube; CONGENITAL HEART-DEFECTS; CELL-CYCLE PROGRESSION; SERUM RESPONSE FACTOR; AMYLOID PRECURSOR PROTEIN; YIN YANG 1; SUMO-1; MODIFICATION; MEDIATED REGULATION; TRANSCRIPTIONAL ACTIVITY; MESENCHYMAL TRANSITION; LUNG ADENOCARCINOMAS;
D O I
10.2174/1389450119666181026151802
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Post-translational modification by small ubiquitin-like modifier (SUMO) has emerged as a global mechanism for the control and integration of a wide variety of biological processes through the regulation of protein activity, stability and intracellular localization. As SUMOylation is examined in greater detail, it has become clear that the process is at the root of several pathologies including heart, endocrine, and inflammatory disease, and various types of cancer. Moreover, it is certain that perturbation of this process, either globally or of a specific protein, accounts for many instances of congenital birth defects. In order to be successful, practical strategies to ameliorate conditions due to disruptions in this post-translational modification will need to consider the multiple components of the SUMOylation machinery and the extraordinary number of proteins that undergo this modification.
引用
收藏
页码:960 / 969
页数:10
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