Therapeutic silencing of serine/threonine kinase 25 for obesity-associated MASLD
Metabolic dysfunction-associated steatotic liver disease (MASLD) is projected to affect 38% of adults and is now the leading cause of chronic liver disease worldwide.1 MASLD spans a continuum from simple steatosis to metabolic dysfunction-associated steatohepatitis (MASH), which can progress to cirrhosis and hepatocellular carcinoma (HCC). The only FDA-approved therapies for patients with MASH and moderate-to-advanced fibrosis are semaglutide and resmetirom, an oral, liver-directed, thyroid hormone receptor β (THR-β)-selective agonist.
Authors
- Daniel Ferguson (ORCID: https://orcid.org/0000-0003-0336-8487)
- Robert Nathaniel Helsley (ORCID: https://orcid.org/0000-0001-5000-3187)
Institutions
- University of Kentucky (US)
- Washington University in St. Louis (US)
- Markey Cancer Center (US)
Publication Details
- Journal
- Molecular Therapy — Nucleic Acids
- Published
- 2026-11-02
- DOI
- https://doi.org/10.1016/j.omtn.2026.103143
- Primary Topic
- Liver Disease Diagnosis and Treatment
- Type
- article
- Field-Weighted Citation Impact
- 0.00