Abstract Background: CBP/p300 are essential transcriptional coactivators of the androgen receptor and play a critical role in prostate cancer pathogenesis. Small-molecule CBP/p300 degraders have demonstrated potent efficacy against prostate cancer but are limited by toxicity, impeding clinical translation. Methods: To enhance tumor specificity and minimize systemic toxicity, we developed a Degrader-Antibody Conjugate (DAC) by linking a highly potent CBP/p300 degrader to a prostate-specific membrane antigen (PSMA) antibody, generating JZY-2233. In vitro antiproliferative activities were assessed using VCaP and LNCaP prostate cancer cell lines. In vivo efficacy, pharmacodynamics, and toxicity were evaluated in a LNCaP xenograft mouse model. Results: JZY-2233 induced robust growth inhibition in VCaP and LNCaP cells, with picomolar IC50 values. In vivo, treatment with JZY-2233 led to sustained CBP/p300 degradation and suppression of c-Myc and PSA in tumor tissues, with effects persisting up to 168 hours post-dose. A single administration at 10 mg/kg resulted in complete tumor suppression for over 90 days in the LNCaP model, significantly exceeding the effect of the unconjugated parent degrader. Importantly, JZY-2233 markedly reduced systemic toxicity. Conclusions: JZY-2233 is a highly potent, antigen-targeted CBP/p300-PSMA DAC, offering prolonged tumor suppression and reduced toxicity in models of advanced prostate cancer. This approach provides a strong rationale for further evaluation in clinical studies and may be adapted for targeting additional tumor antigens across diverse cancers. Citation Format: Mi Wang, Jianzhang Yang, Brandon Bordeau, Shicheng Jin, Yu Wang, Shaomeng Wang. JZY-2233: An antigen-targeted CBP/p300 degrader-antibody conjugate for advanced prostate cancer therapy abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 450.
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Wang et al. (Fri,) studied this question.
www.synapsesocial.com/papers/69d0aff2659487ece0fa6232 — DOI: https://doi.org/10.1158/1538-7445.am2026-450
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Mi Wang
Jianzhang Yang
Brandon M. Bordeau
Cancer Research
University of Michigan
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