前列腺癌
雄激素受体
医学
癌症研究
生物信息学
疾病
临床试验
癌症
雄激素
前列腺
功能(生物学)
选择性拼接
染色质
受体
计算生物学
信号转导
基因表达调控
RNA剪接
信号通路
作者
Isla Henry,Rebecca Foreman,Lakshana Balachandran,Ethan Mortimer,Mohammad Asim,Isla Henry,Rebecca Foreman,Lakshana Balachandran,Ethan Mortimer,Mohammad Asim
出处
期刊:Cancers
[Multidisciplinary Digital Publishing Institute]
日期:2025-11-25
卷期号:17 (23): 3755-3755
标识
DOI:10.3390/cancers17233755
摘要
Castration-resistant prostate cancer (CRPC) remains a major clinical challenge, with disease progression frequently occurring despite the use of potent androgen receptor (AR)-targeted therapies. As AR signalling continues to drive tumour growth in this setting, new therapeutic strategies are being developed to disrupt the AR axis through both direct and indirect mechanisms. This review highlights a selection of promising agents in preclinical or clinical development that represent the next generation of therapies targeting AR signalling. Direct approaches include novel agents that degrade the AR or target domains beyond the conventional ligand-binding domain, aiming to overcome resistance to existing anti-androgens. Indirect strategies are designed to interfere with AR function by modulating AR-associated transcriptional co-regulators, chromatin accessibility, and other regulatory proteins, such as splicing factors, that are critical for sustaining AR-driven gene expression in prostate cancer. Together, these therapies form the basis of emerging strategies to more effectively suppress AR activity in CRPC. This review discusses AR-activating mechanisms, the mechanisms of action of these agents, their clinical development status, and their potential to reshape future treatment paradigms in CRPC.
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