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The Indenoisoquinoline TOP1 Inhibitors Selectively Target Homologous Recombination-Deficient and Schlafen 11-Positive Cancer Cells and Synergize with Olaparib.

Laetitia MarziLudmila SzabovaMelanie GordonZoe Weaver OhlerShyam K SharanMichael L BeshiriMoudjib EtemadiJunko MuraiKathleen KellyYves Pommier
Published in: Clinical cancer research : an official journal of the American Association for Cancer Research (2019)
Our results provide a rationale for molecularly designed clinical trials with the indenoisoquinolines as single agents and in combination with PARP inhibitors in HRD cancers expressing SLFN11.
Keyphrases
  • dna repair
  • dna damage
  • clinical trial
  • oxidative stress
  • phase ii
  • randomized controlled trial
  • open label
  • young adults
  • wild type
  • phase iii