Induced proximity-based therapeutics for advanced prostate cancer

John Ching1, Cindy H Chau2, William D Figg3,4

  • 1Clinical Pharmacology Program, Office of the Clinical Director, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, US.

Npj Drug Discovery
|August 14, 2026
PubMed

Insights

Induced proximity therapeutics offer a novel strategy to target androgen receptor (AR) signaling in metastatic castration-resistant prostate cancer (mCRPC). These advanced approaches show promise in overcoming treatment resistance for mCRPC patients.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • Metastatic castration-resistant prostate cancer (mCRPC) remains dependent on androgen receptor (AR) signaling.
  • Existing therapies targeting AR signaling often face resistance in mCRPC.

Purpose of the Study:

  • To review recent advancements in induced proximity strategies for targeting AR in mCRPC.
  • To explore the potential of event-driven pharmacology in overcoming AR-related resistance.

Main Methods:

  • Review of current literature on induced proximity-based therapeutics.
  • Analysis of mechanisms of action for AR-targeting induced proximity agents.
  • Discussion of preclinical and clinical data related to these strategies.

Main Results:

  • Induced proximity strategies represent a promising therapeutic modality for mCRPC.
  • These approaches leverage event-driven pharmacology to enhance AR degradation or inhibition.
  • Recent advances show potential for overcoming resistance to conventional AR-targeted therapies.

Conclusions:

  • Induced proximity-based therapeutics are emerging as a significant strategy in mCRPC treatment.
  • Further research and clinical evaluation are warranted to fully realize the potential of these novel agents.
  • Targeting AR signaling through induced proximity may offer new hope for patients with resistant prostate cancer.

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