Pristimerin synergizes with gemcitabine through abrogating Chk1/53BP1-mediated DNA repair in pancreatic cancer cells

Food Chem Toxicol. 2021 Jan:147:111919. doi: 10.1016/j.fct.2020.111919. Epub 2020 Dec 7.

Abstract

It has been shown that checkpoint kinase inhibitors can enhance chemosensitivity to gemcitabine by disrupting the replication stress response (RSR). In the present study, we aimed to describe the chemical synthetic lethal effects of the combination of gemcitabine and quinone-methide triterpenoid pristimerin in pancreatic cancer (PC) cells. The drug interaction assay indicated effective synergy between gemcitabine and pristimerin at sub-IC50 concentrations. Interestingly, pristimerin induced lysosomal degradation of checkpoint kinase 1 (Chk1), decreased the percentage of cells at the G1/S boundary and triggered significant double-stranded DNA breaks compared to gemcitabine treatment alone. Moreover, gemcitabine activated the phosphorylation of Chk1 and induced the formation of poly (ADP-ribose) polymers (PARs) as well as the accumulation of 53BP1, which was either partially or completely impaired by pristimerin. Meanwhile, pristimerin augmented the expression of γH2AX upon gemcitabine treatment. Finally, the combination of gemcitabine with pristimerin increased the apoptotic potential of PC cells. These results show that pristimerin acts as a naturally occurring inhibitor of RSR, and a novel therapeutic strategy of combining pristimerin and gemcitabine deserves further detailed investigation in PC models in vivo.

Keywords: 53BP1; Chk1; DNA repair; Gemcitabine; Pristimerin; Replication stress response.

MeSH terms

  • Antimetabolites, Antineoplastic / administration & dosage
  • Antimetabolites, Antineoplastic / pharmacokinetics
  • Antimetabolites, Antineoplastic / pharmacology
  • Cell Line, Tumor
  • Cell Survival
  • Checkpoint Kinase 1 / genetics
  • Checkpoint Kinase 1 / metabolism*
  • DNA Repair / drug effects*
  • Deoxycytidine / administration & dosage
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / pharmacokinetics
  • Deoxycytidine / pharmacology
  • Drug Synergism
  • Gemcitabine
  • Humans
  • Pancreatic Neoplasms / drug therapy*
  • Pentacyclic Triterpenes / administration & dosage
  • Pentacyclic Triterpenes / pharmacokinetics*
  • Pentacyclic Triterpenes / pharmacology
  • Tumor Suppressor p53-Binding Protein 1 / genetics
  • Tumor Suppressor p53-Binding Protein 1 / metabolism*

Substances

  • Antimetabolites, Antineoplastic
  • Pentacyclic Triterpenes
  • TP53BP1 protein, human
  • Tumor Suppressor p53-Binding Protein 1
  • Deoxycytidine
  • CHEK1 protein, human
  • Checkpoint Kinase 1
  • celastrol
  • Gemcitabine