Estébanez-Perpiñá Eva, Bevan Charlotte L, McEwan Iain J
Biochemistry and Molecular Biomedicine, Institute of Biomedicine of the University of Barcelona (IBUB), Edifici Helix, Carrer Baldiri Reixac 15-21, 08028 Barcelona, Spain.
Imperial Centre for Translational & Experimental Medicine (ICTEM), Imperial College London, London W12 0NN, UK.
Cancers (Basel). 2021 Jan 29;13(3):509. doi: 10.3390/cancers13030509.
Prostate cancer (PCa) is the most common cancer in men in the West, other than skin cancer, accounting for over a quarter of cancer diagnoses in US men. In a seminal paper from 1941, Huggins and Hodges demonstrated that prostate tumours and metastatic disease were sensitive to the presence or absence of androgenic hormones. The first hormonal therapy for PCa was thus castration. In the subsequent eighty years, targeting the androgen signalling axis, where possible using drugs rather than surgery, has been a mainstay in the treatment of advanced and metastatic disease. Androgens signal via the androgen receptor, a ligand-activated transcription factor, which is the direct target of many such drugs. In this review we discuss the role of the androgen receptor in PCa and how the combination of structural information and functional screenings is continuing to be used for the discovery of new drug to switch off the receptor or modify its function in cancer cells.
前列腺癌(PCa)是西方男性中除皮肤癌外最常见的癌症,占美国男性癌症诊断病例的四分之一以上。在1941年的一篇开创性论文中,哈金斯和霍奇斯证明前列腺肿瘤和转移性疾病对雄激素的存在或缺失敏感。因此,前列腺癌的第一种激素疗法是去势。在随后的八十年里,尽可能使用药物而非手术来靶向雄激素信号轴,一直是晚期和转移性疾病治疗的主要手段。雄激素通过雄激素受体发出信号,雄激素受体是一种配体激活的转录因子,是许多此类药物的直接靶点。在这篇综述中,我们讨论了雄激素受体在前列腺癌中的作用,以及结构信息和功能筛选的结合如何继续用于发现新药物,以关闭该受体或改变其在癌细胞中的功能。