Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Department of Chemistry, Zhejiang Normal University, 688 Yingbin Road, Jinhua, 321004, PR China; Drug Development and Innovation Center, College of Chemistry and Life Sciences, Zhejiang Normal University, 688 Yingbin Road, Jinhua, 321004, PR China.
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Department of Chemistry, Zhejiang Normal University, 688 Yingbin Road, Jinhua, 321004, PR China; Drug Development and Innovation Center, College of Chemistry and Life Sciences, Zhejiang Normal University, 688 Yingbin Road, Jinhua, 321004, PR China.
Eur J Med Chem. 2023 Feb 5;247:115077. doi: 10.1016/j.ejmech.2022.115077. Epub 2022 Dec 30.
The androgen receptor (AR) is dominant in prostate cancer (PCa) pathology. Current therapeutic agents for advanced PCa include androgen synthesis inhibitors and AR antagonists that bind to the hormone binding pocket (HBP) at the ligand binding domain (LBD). However, AR amplification, AR splice variants (AR-Vs) expression, and intra-tumoral de novo synthesis of androgens result in the reactivation of AR signalling. The AR N-terminal domain (NTD) plays an essential role in AR transcriptional activity. The AR inhibitor targeting NTD could potentially block the activation of both full-length AR and AR-Vs, thus overcoming major resistance mechanisms to current treatments. This review discusses the progress of research in various NTD inhibitors and provides new insight into the development of AR-NTD inhibitors.
雄激素受体 (AR) 在前列腺癌 (PCa) 病理中占主导地位。目前用于晚期 PCa 的治疗药物包括雄激素合成抑制剂和 AR 拮抗剂,它们与配体结合域 (LBD) 中的激素结合口袋 (HBP) 结合。然而,AR 扩增、AR 剪接变体 (AR-Vs) 的表达和肿瘤内雄激素的从头合成导致 AR 信号的重新激活。AR N 端结构域 (NTD) 在 AR 转录活性中起关键作用。针对 NTD 的 AR 抑制剂可能会阻止全长 AR 和 AR-Vs 的激活,从而克服当前治疗方法的主要耐药机制。本文综述了各种 NTD 抑制剂的研究进展,并为 AR-NTD 抑制剂的开发提供了新的见解。