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Cancer-Associated SF3B1 Mutations Confer a BRCA-Like Cellular Phenotype and Synthetic Lethality to PARP Inhibitors.

Katrina M LappinEliana M BarrosSatpal S JhujhGareth W IrwinHayley McMillanFabio Giuseppe LiberanteCheryl LatimerMelissa J La BonteKenneth Ian MillsD Paul HarkinGrant S StewartKienan I Savage
Published in: Cancer research (2022)
The cancer-associated SF3B1K700E mutation induces DNA damage via generation of genotoxic R-loops and stalled replication forks, defective homologous recombination, and increased replication fork degradation, which can be targeted with PARP inhibitors.
Keyphrases
  • dna damage
  • dna repair
  • oxidative stress
  • cancer therapy
  • drug delivery
  • breast cancer risk