Idarubicin combats abiraterone and enzalutamide resistance in prostate cells via targeting XPA protein

Cell Death Dis. 2022 Dec 12;13(12):1034. doi: 10.1038/s41419-022-05490-5.

Abstract

Although second-generation therapies like abiraterone (ABI) and enzalutamide (ENZ) benefit patients with castration-resistant prostate cancer (CRPC), drug resistance frequently occurs, eventually resulting in therapy failure. In this study, we used two libraries, FDA-approved drug library and CRISP/Cas9 knockout (GeCKO) library to screen for drugs that overcome treatment resistance and to identify the potential drug-resistant genes involved in treatment resistance. Our screening results showed that the DNA-damaging agent idarubicin (IDA) overcame abiraterone and enzalutamide resistance in prostate cancer cells. IDA treatment inhibited the DNA repair protein XPA expression in a transcription-independent manner. Consistently, XPA knockout sensitized prostate cancer cells to abiraterone and enzalutamide treatment. In conclusion, IDA combats abiraterone and enzalutamide resistance by reducing XPA protein level in prostate cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Docetaxel
  • Humans
  • Idarubicin / therapeutic use
  • Male
  • Nitriles / therapeutic use
  • Prostate
  • Prostatic Neoplasms, Castration-Resistant* / drug therapy
  • Prostatic Neoplasms, Castration-Resistant* / genetics
  • Taxoids / therapeutic use
  • Xeroderma Pigmentosum Group A Protein

Substances

  • Idarubicin
  • Docetaxel
  • Taxoids
  • enzalutamide
  • Nitriles
  • XPA protein, human
  • Xeroderma Pigmentosum Group A Protein