VCP/p97 as a therapeutic target in KRAS-mutant pancreatic cancer: Study

Researchers have recently shown that proteins involved in the DNA damage response (DDR) are critical for KRAS-mutant pancreatic ductal adenocarcinoma (PDAC) cell growth in vitro. However, the CRISPR-Cas9 library that enabled the identification of these key proteins contained limited representation of DDR-related genes. In their recent study, researchers from the University of North Carolina at Chapel Hill performed a comprehensive, DDR-focused CRISPR-Cas9 loss-of-function screen to further investigate the DDR in this context.

This screen identified valosin-containing protein (VCP) as an essential gene in KRAS-mutant PDAC cell lines. The team observed that genetic and pharmacologic inhibition of VCP limited cell growth and induced apoptotic death. To address the basis for VCP-dependent growth, they first evaluated the contribution of VCP to the DDR and found that loss of VCP resulted in accumulation of DNA double-strand breaks.

Next, they addressed its role in proteostasis and found that loss of VCP caused accumulation of polyubiquitinated proteins. The researchers also found that loss of VCP increased autophagy. Therefore, the team reasoned that inhibiting both VCP and autophagy could be an effective combination. Accordingly, they found that VCP inhibition synergized with the autophagy inhibitor chloroquine. Their conclusion was that concurrent targeting of autophagy can enhance the efficacy of VCP inhibitors in KRAS-mutant PDAC.

Reference:

VCP/p97, a pleiotropic protein regulator of the DNA damage response and proteostasis, is a potential therapeutic target in KRAS-mutant pancreatic cancer,Genes & Cancer,doi10.18632/genesandcancer.231