Proteasome Activation as a New Therapeutic Approach To Target Proteotoxic Disorders

被引:89
作者
Njomen, Evert [1 ]
Tepe, Jetze J. [1 ]
机构
[1] Michigan State Univ, Dept Chem & Pharmacol & Toxicol, E Lansing, MI 48824 USA
基金
美国国家卫生研究院;
关键词
UBIQUITIN-INDEPENDENT DEGRADATION; SMALL-MOLECULE INHIBITOR; 20S PROTEASOME; PROTEIN AGGREGATION; 26S PROTEASOMES; LIFE-SPAN; POTENTIAL APPLICATION; PEPTIDASE ACTIVITIES; OXIDIZED PROTEINS; OXIDATIVE STRESS;
D O I
10.1021/acs.jmedchem.9b00101
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Proteasomes are multienzyme complexes that maintain protein homeostasis (proteostasis) and important cellular functions through the degradation of misfolded, redundant, and damaged proteins. It is well established that aging is associated with the accumulation of damaged and misfolded proteins. This phenomenon is paralleled by declined proteasome activity. When the accumulation of redundant proteins exceed degradation, undesirable signaling and/or aggregation occurs and are the hallmarks of neurodegenerative diseases and many cancers. Thus, increasing proteasome activity has been recognized as a new approach to delay the onset or ameliorate the symptoms of neurodegenerative and other proteotoxic disorders. Enhancement of proteasome activity has many therapeutic potentials but is still a relatively unexplored field. In this perspective, we review current approaches, genetic manipulation, posttranslational modification, and small molecule proteasome agonists used to increase proteasome activity, challenges facing the field, and applications beyond aging and neurodegenerative diseases.
引用
收藏
页码:6469 / 6481
页数:13
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