Design of amidobenzimidazole STING receptor agonists with systemic activity
- PMID: 30405246
- DOI: 10.1038/s41586-018-0705-y
Design of amidobenzimidazole STING receptor agonists with systemic activity
Erratum in
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Author Correction: Design of amidobenzimidazole STING receptor agonists with systemic activity.Nature. 2019 Jun;570(7761):E53. doi: 10.1038/s41586-019-1265-5. Nature. 2019. PMID: 31142845
Abstract
Stimulator of interferon genes (STING) is a receptor in the endoplasmic reticulum that propagates innate immune sensing of cytosolic pathogen-derived and self DNA1. The development of compounds that modulate STING has recently been the focus of intense research for the treatment of cancer and infectious diseases and as vaccine adjuvants2. To our knowledge, current efforts are focused on the development of modified cyclic dinucleotides that mimic the endogenous STING ligand cGAMP; these have progressed into clinical trials in patients with solid accessible tumours amenable to intratumoral delivery3. Here we report the discovery of a small molecule STING agonist that is not a cyclic dinucleotide and is systemically efficacious for treating tumours in mice. We developed a linking strategy to synergize the effect of two symmetry-related amidobenzimidazole (ABZI)-based compounds to create linked ABZIs (diABZIs) with enhanced binding to STING and cellular function. Intravenous administration of a diABZI STING agonist to immunocompetent mice with established syngeneic colon tumours elicited strong anti-tumour activity, with complete and lasting regression of tumours. Our findings represent a milestone in the rapidly growing field of immune-modifying cancer therapies.
Comment in
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Cancer immunotherapy: STINGing systemically.Nat Rev Drug Discov. 2018 Dec 28;18(1):15. doi: 10.1038/nrd.2018.236. Nat Rev Drug Discov. 2018. PMID: 30591729 No abstract available.
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