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Mol Cancer Ther ; 20(5): 763-774, 2021 05.
Article in English | MEDLINE | ID: mdl-33649102

ABSTRACT

Numerous mechanisms of resistance arise in response to treatment with second-generation androgen receptor (AR) pathway inhibitors in metastatic castration-resistant prostate cancer (mCRPC). Among these, point mutations in the ligand binding domain can transform antagonists into agonists, driving the disease through activation of AR signaling. To address this unmet need, we report the discovery of JNJ-63576253, a next-generation AR pathway inhibitor that potently abrogates AR signaling in models of human prostate adenocarcinoma. JNJ-63576253 is advancing as a clinical candidate with potential effectiveness in the subset of patients who do not respond to or are progressing while on second-generation AR-targeted therapeutics.


Subject(s)
Androgen Receptor Antagonists/therapeutic use , Prostatic Neoplasms, Castration-Resistant/drug therapy , Protein Domains/genetics , Androgen Receptor Antagonists/pharmacology , Animals , Cell Line, Tumor , Humans , Ligands , Male , Mice , Models, Molecular , Mutation , Rats , Xenograft Model Antitumor Assays
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