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JNJ-63576253的发现,一种新一代雄激素受体拮抗剂,对转移性去势抵抗性前列腺癌中的野生型和临床相关配体结合域突变均有活性。

Discovery of JNJ-63576253, a Next-Generation Androgen Receptor Antagonist Active Against Wild-Type and Clinically Relevant Ligand Binding Domain Mutations in Metastatic Castration-Resistant Prostate Cancer.

作者信息

Branch Jonathan R, Bush Tammy L, Pande Vineet, Connolly Peter J, Zhang Zhuming, Hickson Ian, Ondrus Janine, Jaensch Steffen, Bischoff James R, Habineza Georges, Van Hecke Geert, Meerpoel Lieven, Packman Kathryn, Parrett Christopher J, Chong Yolanda T, Gottardis Marco M, Bignan Gilles

机构信息

Janssen Research and Development, Spring House, Pennsylvania.

Janssen Research and Development, Beerse, Belgium.

出版信息

Mol Cancer Ther. 2021 May;20(5):763-774. doi: 10.1158/1535-7163.MCT-20-0510. Epub 2021 Mar 1.

DOI:10.1158/1535-7163.MCT-20-0510
PMID: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.

摘要

在转移性去势抵抗性前列腺癌(mCRPC)中,使用第二代雄激素受体(AR)通路抑制剂进行治疗时会出现多种耐药机制。其中,配体结合域中的点突变可将拮抗剂转化为激动剂,通过激活AR信号传导推动疾病进展。为满足这一未被满足的需求,我们报告了JNJ-63576253的发现,这是一种新一代AR通路抑制剂,在人前列腺腺癌模型中能有效消除AR信号传导。JNJ-63576253正在作为临床候选药物推进,对那些对第二代AR靶向治疗无反应或正在进展的患者亚组具有潜在疗效。

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Elevated labile iron in castration-resistant prostate cancer is targetable with ferrous iron-activatable antiandrogen therapy.
去势抵抗性前列腺癌中不稳定铁的升高可以通过亚铁离子激活的抗雄激素治疗来靶向治疗。
Eur J Med Chem. 2023 Mar 5;249:115110. doi: 10.1016/j.ejmech.2023.115110. Epub 2023 Jan 14.