p97: An Emerging Target for Cancer, Neurodegenerative Diseases, and Viral Infections

被引:69
|
作者
Huryn, Donna M. [1 ,2 ]
Kornfilt, David J. P. [3 ]
Wipf, Peter [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Chem Divers Ctr, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Pharmaceut Sci, Pittsburgh, PA 15260 USA
[3] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
关键词
VALOSIN-CONTAINING PROTEIN; AAA-ATPASE; INDOLE INHIBITORS; VCP/P97; COVALENT; ANALOGS; IDENTIFICATION; DERIVATIVES; WITHAFERIN; EVOLUTION;
D O I
10.1021/acs.jmedchem.9b01318
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The AAA+ ATPase, p97, also referred to as VCP, plays an essential role in cellular homeostasis by regulating endoplasmic reticulum-associated degradation (ERAD), mitochondrial-associated degradation ( MAD), chromatin-associated degradation, autophagy, and endosomal trafficking. Mutations in p97 have been linked to a number of neurodegenerative diseases, and overexpression of wild type p97 is observed in numerous cancers. Furthermore, p97 activity has been shown to be essential for the replication of certain viruses, including poliovirus, herpes simplex virus (HSV), cytomegalovirus (CMV), and influenza. Taken together, these observations highlight the potential for targeting p97 as a therapeutic approach in neurodegeneration, cancer, and certain infectious diseases. This Perspective reviews recent advances in the discovery of small molecule inhibitors of p97, their optimization and characterization, and therapeutic potential.
引用
收藏
页码:1892 / 1907
页数:16
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