Qian Chao, Wang Zhen, Xiong Yan, Zhang Dingpeng, Zhong Yue, Inuzuka Hiroyuki, Qi Yihang, Xie Ling, Chen Xian, Wei Wenyi, Jin Jian
Mount Sinai Center for Therapeutics Discovery, Departments of Pharmacological Sciences, Oncological Sciences and Neuroscience, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, United States.
Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, United States.
J Am Chem Soc. 2025 Apr 30;147(17):14564-14573. doi: 10.1021/jacs.5c01662. Epub 2025 Apr 19.
Deubiquitinase-targeting chimera (DUBTAC) has emerged as a promising technology for targeted protein stabilization (TPS) by harnessing deubiquitinases (DUBs) to remove polyubiquitin chains from target proteins. Despite the presence of over 100 human DUBs, only OTUB1 and USP7 have been utilized in the development of DUBTAC. Hence, there is an urgent need to harness additional DUBs to expand the DUBTAC arsenal. In this work, we demonstrate for the first time that the USP1 deubiquitinase, which is overexpressed in several human cancers, can be leveraged for TPS. We report the development of novel USP1-recruiting DUBTACs by utilizing a noncovalent small-molecule inhibitor of USP1. First, we generated a USP1-based CFTR DUBTAC, MS5310, which effectively stabilized CFTR and is more potent than previously reported CFTR DUBTACs. Next, we developed first-in-class USP1-recruiting UTX DUBTACs, including MS7131, from a small-molecule inhibitor of UTX and JMJD3. Notably, MS7131 effectively stabilized the tumor suppressor UTX in a concentration- and time-dependent manner, while sparing the oncoprotein JMJD3, despite it retaining potent inhibition of JMJD3. Furthermore, UTX stabilization induced by MS7131 was dependent on the engagement of both USP1 and UTX. Consequently, MS7131, but not the parent USP1 inhibitor or UTX inhibitor, effectively reduced histone H3 lysine 27 trimethylation and significantly suppressed the proliferation and clonogenicity of cancer cells. Overall, this study highlights that USP1 can be harnessed for DUBTAC development. Moreover, we developed a valuable chemical tool, MS7131, for the investigation of UTX's distinct functions. This advancement paves the way for leveraging DUBTACs in the treatment of related diseases.
去泛素酶靶向嵌合体(DUBTAC)已成为一种很有前景的靶向蛋白质稳定化(TPS)技术,它通过利用去泛素酶(DUB)从靶蛋白上去除多聚泛素链。尽管人类有100多种DUB,但在DUBTAC的开发中仅使用了OTUB1和USP7。因此,迫切需要利用其他DUB来扩充DUBTAC武器库。在这项工作中,我们首次证明,在几种人类癌症中过表达的USP1去泛素酶可用于TPS。我们报告了通过使用USP1的非共价小分子抑制剂开发新型USP1招募型DUBTAC。首先,我们生成了一种基于USP1的CFTR DUBTAC,即MS5310,它能有效稳定CFTR,且比先前报道的CFTR DUBTAC更有效。接下来,我们从UTX和JMJD3的小分子抑制剂开发出了一流的USP1招募型UTX DUBTAC,包括MS7131。值得注意的是,MS7131以浓度和时间依赖性方式有效稳定了肿瘤抑制因子UTX,同时使癌蛋白JMJD3不受影响,尽管它对JMJD3仍有强效抑制作用。此外,MS7131诱导的UTX稳定依赖于USP1和UTX的结合。因此,MS7131而非母体USP1抑制剂或UTX抑制剂有效降低了组蛋白H3赖氨酸27三甲基化,并显著抑制了癌细胞的增殖和克隆形成能力。总体而言,这项研究突出表明USP1可用于DUBTAC开发。此外,我们开发了一种有价值的化学工具MS7131,用于研究UTX的独特功能。这一进展为在相关疾病治疗中利用DUBTAC铺平了道路。