p97: An Emerging Target for Cancer, Neurodegenerative Diseases, and Viral Infections.
Donna M HurynDavid J P KornfiltPeter WipfPublished in: Journal of medicinal chemistry (2019)
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.
Keyphrases
- small molecule
- herpes simplex virus
- endoplasmic reticulum
- papillary thyroid
- infectious diseases
- wild type
- oxidative stress
- squamous cell
- transcription factor
- gene expression
- sars cov
- cell death
- dna damage
- cell proliferation
- epstein barr virus
- lymph node metastasis
- protein protein
- genome wide
- systematic review
- dna methylation
- risk assessment