化学
结直肠癌
癌症研究
癌症
内科学
医学
生物
作者
Byul Moon,Ahra Go,Seulki Park,Hyun Jin Kim,Dongju An,Jaehoon Kim,Joo-Youn Lee,Jeong‐Hoon Kim,Jong Yeon Hwang,Jung‐Ae Kim
标识
DOI:10.1016/j.bmcl.2025.130141
摘要
The Werner protein, WRN, is a member of the RecQ helicase family implicated in genome maintenance. Several large-scale functional genomics screens have identified WRN as a synthetic lethal target in cancer cell lines with microsatellite instability-high (MSI-H). Accordingly, WRN is considered a potential therapeutic target in MSI-H cancers. HRO761, a non-covalent WRN inhibitor developed by Novartis, entered clinical trial for patients with MSI-H colorectal cancer (CRC). In this study, we investigated bioisosteric replacement of the hydroxyl pyrimidine residue of HRO761 with several bicyclic structures to obtain a novel chemical entity. In vitro ATPase and cell proliferation assays revealed two candidate chemicals that showed similar or better effects than HRO761. Additionally, an in vivo study demonstrated that KWR095, a newly synthesized WRN inhibitor, has significant anti-proliferative effects compared with vehicle.
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