PUBLICATION

Zebrafish as an in vivo screening tool to establish PARP inhibitor efficacy

Authors
Vierstraete, J., Fieuws, C., Willaert, A., Vral, A., Claes, K.B.M.
ID
ZDB-PUB-201221-2
Date
2020
Source
DNA repair   97: 103023 (Journal)
Registered Authors
Willaert, Andy
Keywords
Homologous Recombination, Irradiation, PARP inhibitor, Zebrafish
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Antineoplastic Agents/pharmacology
  • BRCA2 Protein/genetics
  • DNA/metabolism
  • DNA/radiation effects
  • Drug Evaluation, Preclinical/methods*
  • Models, Animal*
  • Mutation*
  • Phthalazines/pharmacology
  • Piperazines/pharmacology
  • Poly(ADP-ribose) Polymerase Inhibitors/pharmacology*
  • Recombinational DNA Repair*
  • Zebrafish/genetics*
  • Zebrafish/metabolism
  • Zebrafish Proteins/genetics
PubMed
33341473 Full text @ DNA Repair (Amst).
Abstract
Double strand break (DSB) repair through Homologous Recombination (HR) is essential in maintaining genomic stability of the cell. Mutations in the HR pathway confer an increased risk for breast, ovarian, pancreatic and prostate cancer. PARP inhibitors (PARPi) are compounds that specifically target tumours deficient in HR. Novel PARPi are constantly being developed, but research is still heavily focussed on in vitro data, with mouse xenografts only being used in late stages of development. There is a need for assays that can: 1) provide in vivo data, 2) early in the development process of novel PARPi, 3) provide fast results and 4) at an affordable cost. Here we propose a combination of in vivo zebrafish assays to accurately quantify PARP inhibitor efficacy. We showed that PARPi display functional effects in zebrafish, generally correlating with their PARP trapping capacities. Furthermore, we displayed how olaparib mediated radiosensitization is conserved in our zebrafish model. These assays could aid the development of novel PARPi by providing early in vivo data. In addition, using zebrafish allows for high-throughput testing of combination therapies in search of novel treatment strategies.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping