Development of PROTACs targeting estrogen receptor: an emerging technique for combating endocrine resistance.

IF 4.1 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Rouming Peng, Xin Liu, Chun-Chi Chen, Rey-Ting Guo, Jian Min
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引用次数: 0

Abstract

Despite the success of endocrine therapies in treating ER-positive breast cancer, the development of resistance remains a significant challenge. Estrogen receptor targeting proteolysis-targeting chimeras (ER PROTACs) offer a unique approach by harnessing the ubiquitin-proteasome system to degrade ER, potentially bypassing resistance mechanisms. In this review, we present the drug design, efficacy and early clinical trials of these ER PROTACs. This review underscores the academic and industrial opportunities presented by this emerging technology, as well as the challenges that must be addressed to translate these findings into effective clinical therapies.

靶向雌激素受体的PROTACs的开发:对抗内分泌抵抗的新技术。
尽管内分泌疗法在治疗雌激素受体阳性乳腺癌方面取得了成功,但耐药性的发展仍然是一个重大挑战。雌激素受体靶向蛋白水解嵌合体(ER PROTACs)提供了一种独特的方法,利用泛素-蛋白酶体系统来降解ER,可能绕过耐药机制。在这篇综述中,我们介绍了这些ER protac的药物设计、疗效和早期临床试验。这篇综述强调了这一新兴技术所带来的学术和工业机遇,以及必须解决的挑战,将这些发现转化为有效的临床治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.80
自引率
2.40%
发文量
129
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