Discovery of novel WRN inhibitors for treating MSI-H colorectal cancers
- Bioorg Med Chem Lett. 2025 Feb 15:120:130141. doi: 10.1016/j.bmcl.2025.130141.
- 1. Aging Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, South Korea.
- 2. Therapeutics and Biotechnology Division, Korea Research Institute of Chemical Technology, Daejeon 34114, Republic of Korea.
- 3. DiseaseTarget Structure Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 34141, South Korea.
- 4. Therapeutics and Biotechnology Division, Korea Research Institute of Chemical Technology, Daejeon 34114, Republic of Korea; Medicinal Chemistry and Pharmacology, Korea University of Science and Technology, Daejeon 34113, Republic of Korea.
- 5. Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon 34141, South Korea.
- 6. DiseaseTarget Structure Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 34141, South Korea; KRIBB School of Bioscience, Korea University of Science and Technology (UST), Daejeon 34113, South Korea. Electronic address: [email protected].
- 7. Therapeutics and Biotechnology Division, Korea Research Institute of Chemical Technology, Daejeon 34114, Republic of Korea; Medicinal Chemistry and Pharmacology, Korea University of Science and Technology, Daejeon 34113, Republic of Korea. Electronic address: [email protected].
- 8. Aging Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, 34141, South Korea; KRIBB School of Bioscience, Korea University of Science and Technology (UST), Daejeon 34113, South Korea. Electronic address: [email protected].
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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Cat. No.Product NameDescriptionTargetResearch Area
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target: DNA/RNA SynthesisResearch Areas: Cancer
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target: DNA/RNA SynthesisResearch Areas: Cancer