Wang Yixing, Hess Jessica D, Wang Chen, Ma Lingzi, Luo Megan, Jossart Jennifer, Perry John J, Kwon David, Wang Zhe, Pei Xinyu, Shen Changxian, Wang Yingying, Zhou Mian, Yin Holly, Horne David, Nussenzweig André, Zheng Li, Shen Binghui
Department of Cancer Genetics and Epigenetics, Beckman Research Institute, City of Hope, Duarte, California 91010, United States.
Department of Molecular Diagnostics and Experimental Therapeutics, Beckman Research Institute, City of Hope, Duarte, California 91010, United States.
ACS Chem Biol. 2025 Jun 20;20(6):1258-1272. doi: 10.1021/acschembio.5c00117. Epub 2025 May 16.
Human exonuclease 1 (EXO1), a member of the structure-specific nuclease family, plays a critical role in maintaining genome stability by processing DNA double-strand breaks (DSBs), nicks, and replication intermediates during DNA replication and repair. As its exonuclease activity is essential for homologous recombination (HR) and replication fork processing, EXO1 has emerged as a compelling therapeutic target, especially in cancers marked by heightened DNA damage and replication stress. Through high-throughput screening of 45,000 compounds, we identified seven distinct chemical scaffolds that demonstrated effective and selective inhibition of EXO1. Representative compounds from two of the most potent scaffolds, C200 and F684, underwent a comprehensive docking analysis and subsequent site-directed mutagenesis studies to evaluate their binding mechanisms. Biochemical assays further validated their potent and selective inhibition of the EXO1 nuclease activity. Tumor cell profiling experiments revealed that these inhibitors exploit synthetic lethality in BRCA1-deficient cells, emphasizing their specificity and therapeutic potential for targeting genetically HR-deficient (HRD) cancers driven by deleterious mutations in HR genes like BRCA1/2. Mechanistically, EXO1 inhibition suppressed DNA end resection, stimulated the accumulation of DNA double-strand breaks, and triggered S-phase PARylation, effectively disrupting DNA repair pathways that are essential for cancer cell survival. These findings establish EXO1 inhibitors as promising candidates for the treatment of HRD cancers and lay the groundwork for the further optimization and development of these compounds as targeted therapeutics.
人核酸外切酶1(EXO1)是结构特异性核酸酶家族的成员,在DNA复制和修复过程中通过处理DNA双链断裂(DSB)、切口和复制中间体来维持基因组稳定性方面发挥着关键作用。由于其核酸外切酶活性对于同源重组(HR)和复制叉处理至关重要,EXO1已成为一个引人注目的治疗靶点,尤其是在以DNA损伤加剧和复制应激为特征的癌症中。通过对45000种化合物的高通量筛选,我们鉴定出七种不同的化学支架,它们对EXO1表现出有效且选择性的抑制作用。来自两种最有效的支架C200和F684的代表性化合物进行了全面的对接分析和随后的定点诱变研究,以评估它们的结合机制。生化分析进一步验证了它们对EXO1核酸酶活性的强效和选择性抑制作用。肿瘤细胞分析实验表明,这些抑制剂利用了BRCA1缺陷细胞中的合成致死性,强调了它们针对由BRCA1/2等HR基因有害突变驱动的遗传性HR缺陷(HRD)癌症的特异性和治疗潜力。从机制上讲,EXO1抑制作用抑制了DNA末端切除,刺激了DNA双链断裂的积累,并引发了S期聚腺苷酸化反应,有效地破坏了癌细胞存活所必需的DNA修复途径。这些发现确立了EXO1抑制剂作为治疗HRD癌症的有前景的候选药物,并为进一步优化和开发这些化合物作为靶向治疗药物奠定了基础。