Aberrant human ClpP activation disturbs mitochondrial proteome homeostasis to suppress pancreatic ductal adenocarcinoma

Cell Chem Biol. 2022 Sep 15;29(9):1396-1408.e8. doi: 10.1016/j.chembiol.2022.07.002. Epub 2022 Jul 28.

Abstract

The mitochondrial caseinolytic protease P (ClpP) is a target candidate for treating leukemia; however, the effects of ClpP modulation on solid tumors have not been adequately explored. Here, we report a potent activator of ClpP with the therapeutic potential for pancreatic ductal adenocarcinoma (PDAC). We first validated that aberrant ClpP activation leads to growth arrest of PDAC cells and tumors. We then performed high-throughput screening and synthetic optimization, from which we identified ZG111, a potent activator of ClpP. ZG111 binds to ClpP and promotes the ClpP-mediated degradation of respiratory chain complexes. This degradation activates the JNK/c-Jun pathway, induces the endoplasmic reticulum stress response, and consequently causes the growth arrest of PDAC cells. ZG111 also produces inhibitory effects on tumor growth in cell line-derived and patient-derived xenograft mouse models. Altogether, our data demonstrate a promising therapeutic strategy for PDAC suppression through the chemical activation of ClpP.

Keywords: ClpP activator; cancer therapy; mitochondrial proteome homeostasis; oxidative phosphorylation; pancreatic ductal adenocarcinoma; respiratory chain complexes; target validation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carcinoma, Pancreatic Ductal* / metabolism
  • Endopeptidase Clp / metabolism
  • Homeostasis
  • Humans
  • Mice
  • Pancreatic Neoplasms* / metabolism
  • Peptide Hydrolases / metabolism
  • Proteome / metabolism

Substances

  • Proteome
  • Peptide Hydrolases
  • ClpP protein, human
  • Endopeptidase Clp