Integrative high-throughput studies to develop novel targets and drugs for the treatment of advanced prostate cancer

Xuehui Li1,2,3, Yanting Shen1, Na Zhang4

  • 1Department of Urology and Andrology, Gongli Hospital of Shanghai Pudong New Area, Shanghai 200135, China.

Genes & Diseases
|January 6, 2026
PubMed

Insights

New prostate cancer drugs target CDC20, DTL, and RRM2, which drive tumor growth independently of androgen receptor (AR) signaling. These novel agents show promise against castration-resistant prostate cancer.

Area of Science:

  • Oncology
  • Molecular Biology
  • Bioinformatics

Background:

  • Androgen deprivation therapies (ADT) are standard for prostate cancer but often lead to castration resistance.
  • Novel therapeutic strategies targeting AR-independent pathways are crucial for advanced castration-resistant prostate cancer (CRPC).

Purpose of the Study:

  • To identify and validate novel AR-independent therapeutic targets for advanced prostate cancer.
  • To discover and test novel small-molecule agents against these targets.

Main Methods:

  • Integrative bioinformatics screening of gene dependency (CRISPRi/RNAi), clinical relevance, and experimental validation (CRISPR-Cas13).
  • Mechanistic studies on the RB1/E2F1 axis regulation of identified targets.
  • Virtual screening and drug sensitivity assays using a small-molecule library.

Main Results:

  • Identified CDC20, DTL, and RRM2 as key tumor drivers in advanced prostate cancer.
  • Established the RB1/E2F1 axis as a regulator of cell cycle progression via these targets.
  • Discovered novel agents with superior in vitro anti-tumor efficacy compared to AR antagonists.

Conclusions:

  • CDC20, DTL, and RRM2 represent promising AR-independent therapeutic targets for CRPC.
  • The study presents a novel research paradigm combining bioinformatics and network pharmacology for anti-cancer drug development.