Evidence map›Paper›PMID 42748411›Full record

ArticleHepatology communications2026

Prime editing models the MTARC1 A165T variant in human liver organoids, demonstrating reduced steatosis, inflammation, and fibrosis.

Amel Ben Saad, Nahid Arghiani, Arden D Weilheimer, Stefan D Gentile, Benjamin J Toles, Sudipta Tripathi, Seher Mohsin Sayed, Anil Chandraker, Alan C Mullen

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Article in Hepatology communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Amel Ben SaadDivision of Gastroenterology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Nahid ArghianiDivision of Gastroenterology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Arden D WeilheimerDivision of Gastroenterology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Stefan D GentileThe Broad Institute, Cambridge, Massachusetts, USA.
Benjamin J TolesDivision of Gastroenterology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Sudipta TripathiDivision of Renal Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Seher Mohsin SayedDivision of Renal Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Anil ChandrakerDivision of Renal Medicine, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Alan C MullenDivision of Gastroenterology, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMetabolic dysfunction-associated steatotic liver disease (MASLD) is the most prevalent cause of chronic liver disease worldwide. This progressive, multifactorial condition is characterized by hepatic steatosis, which can evolve into steatohepatitis, fibrosis, cirrhosis, and liver cancer. Genetic factors influence the development, progression, and complications in MASLD, and genome-wide association studies (GWAS) have identified single-nucleotide polymorphisms (SNPs) associated with altered risk. Mitochondrial amidoxime reducing component 1 (MTARC1) rs2642438 (p.A165T) variant has been identified as protective, but the role of MTARC1 and the impact of this variant in hepatocytes remains poorly understood.

methodsWe applied prime editing to create the rs2642438 variant in human embryonic stem cells (hESCs) before differentiation into human liver organoids (HLOs) to investigate the effect of the variant under conditions of steatotic and fibrotic injury.

resultsCompared with HLOs formed from hESCs containing the MTARC1 reference sequence, HLOs with the rs2642438 variant show lower levels of MTARC1 protein and triglycerides and are protected from steatotic and fibrotic injury, as predicted by the phenotype observed in patients carrying the variant. The observed decrease in triglyceride levels with the variant appears to be driven more by suppression of de novo lipogenesis than stimulation of β-oxidation in the HLO model. While resmetirom, the thyroid hormone receptor-beta (THRB) agonist approved to treat patients with metabolic dysfunction-associated steatohepatitis (MASH), was effective in reducing triglyceride levels in the setting of steatotic injury in HLOs with the reference sequence, HLOs containing the variant did not show further reduction in triglyceride levels with exposure to resmetirom.

conclusionsCollectively, these findings establish a platform to model disease-associated SNPs in HLOs, provide insight into the activity of the MTARC1 variant, and suggest that SNP profiling may help identify patients more likely to respond to MASLD therapies.

Indexed as

Fatty LiverLiverLiver CirrhosisOrganoidsOxidoreductasesHepatocytesHuman Embryonic Stem CellsHumansPolymorphism, Single NucleotideOxidoreductasesgenetic polymorphismhuman liver organoidsliverMASLDresmetirom

Identifiers

PMID42748411
PMCPMC13585322

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