摘要
除了晚期疾病去势术后的睾酮水平外,雄激素受体(AR)信号途径也是导致前列腺癌的关键因素。雄激素生物合成抑制剂abiraterone和抗雄激素enzalutamide在紫杉醇化疗前后能延长生存期。现在他们已经被应用于临床。随着这些药物的使用和其他新的生存时间延长疗法的出现,晚期前列腺癌患者现在生活更长,生活质量更好。本文对用于晚期前列腺癌的靶向治疗的临床前和临床数据进行了总结,重点强调了其耐药机制和未来研究方向。
关键词: 前列腺癌,雄激素受体,abiraterone,enzalutamide。
图形摘要
Current Drug Targets
Title:New Compounds Targeting the Androgen Receptor for Treatment of Advanced Prostate Cancer
Volume: 17 Issue: 3
Author(s): Rita Assi, Sally Temraz, Ali Shamseddine and Deborah Mukherji
Affiliation:
关键词: 前列腺癌,雄激素受体,abiraterone,enzalutamide。
摘要: The androgen receptor (AR) signalling pathway remains a key driver of prostate cancer progression despite castrate levels of testosterone in advanced disease. The androgen biosynthesis inhibitor abiraterone and the anti-androgen enzalutamide have been shown to prolong survival in randomized clinical trials both pre-and post-docetaxel chemotherapy and are now in routine clinical use. With the use of these drugs and other novel survival-prolonging therapeutics, patients with advanced prostate cancer are now living longer with better quality of life. This article will review pre-clinical and clinical data for AR-targeting therapeutics for advanced prostate cancer with a focus on mechanisms of resistance and future directions for research.
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Cite this article as:
Rita Assi, Sally Temraz, Ali Shamseddine and Deborah Mukherji , New Compounds Targeting the Androgen Receptor for Treatment of Advanced Prostate Cancer, Current Drug Targets 2016; 17 (3) . https://dx.doi.org/10.2174/1389450116666150907101044
DOI https://dx.doi.org/10.2174/1389450116666150907101044 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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