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Attenuation of SRC Kinase Activity Augments PARP Inhibitor-mediated Synthetic Lethality in BRCA2-altered Prostate Tumors.

Goutam ChakrabortyNabeela Khan PatailRahim HiraniSubhiksha NandakumarYing Z MazzuYuki YoshikawaMohammad O AtiqLina E JehaneKonrad H StopsackGwo-Shu Mary LeeWassim AbidaMichael J MorrisLorelei A MucciDaniel DanilaPhilip W Kantoff
Published in: Clinical cancer research : an official journal of the American Association for Cancer Research (2020)
This work suggests that SRC activation may be a potential mechanism of PARPi resistance and that treatment with SRC inhibitors may overcome this resistance. Our preclinical study demonstrates that combining PARPis and SRC inhibitors may be a promising therapeutic strategy for patients with BRCA2-null mCRPC.
Keyphrases
  • tyrosine kinase
  • prostate cancer
  • dna damage
  • dna repair
  • risk assessment
  • benign prostatic hyperplasia
  • oxidative stress
  • bone marrow
  • breast cancer risk
  • human health
  • climate change