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Synthetic lethal targeting of RNF20 through PARP1 silencing and inhibition.

Brent J GuppyKirk James McManus
Published in: Cellular oncology (Dordrecht) (2017)
Collectively, our data indicate that RNF20 and PARP1 are synthetic lethal interactors, suggesting that cancers with diminished RNF20 expression and/or function may be susceptible to PARP1 inhibitors.
Keyphrases
  • dna repair
  • dna damage
  • dna damage response
  • poor prognosis
  • electronic health record
  • big data
  • oxidative stress
  • machine learning
  • long non coding rna
  • binding protein
  • data analysis
  • young adults
  • artificial intelligence