Targeting PNPLA3 I148M variant in MASLD: Cell-type specific mechanisms and precision therapy opportunities

The PNPLA3 I148M variant is the primary genetic risk factor for metabolic dysfunction-associated steatotic liver disease, representing the most promising target for interventions in this increasingly prevalent disease. In this review, we describe the lipotoxicity effects of the mutant protein in both hepatocytes and hepatic stellate cells (HSCs), driven by its weak triglyceride-hydrolysing activity, altered lipid composition, and resistance to ubiquitin-proteasomal degradation. In the context of MASLD-associated oxidative stress, lipid retention and peroxidation lead to mitochondrial dysfunction, ER stress, and ferroptosis in hepatocytes, while promoting HSC activation and fibrogenesis, thus driving the pathological transition from benign steatosis to MASH. We also summarize mechanism-based therapeutic strategies aimed at supporting the development of personalised, targeted interventions for I148M carriers.

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Publication Details

Journal
Biomedicine & Pharmacotherapy
Published
2026-07-21
DOI
https://doi.org/10.1016/j.biopha.2026.119746
Primary Topic
Liver Disease Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Targeting PNPLA3 I148M variant in MASLD: Cell-type specific mechanisms and precision therapy opportunities

Helin Liu, Ping Wang, Lu Liu, Huainan Bu et al.
Biomedicine & Pharmacotherapy
Liver Disease Diagnosis and Treatment
article

Targeting PNPLA3 I148M variant in MASLD: Cell-type specific mechanisms and precision therapy opportunities

Helin Liu, Ping Wang, Lu Liu, Huainan Bu, Hui Wang
article en

Abstract

The PNPLA3 I148M variant is the primary genetic risk factor for metabolic dysfunction-associated steatotic liver disease, representing the most promising target for interventions in this increasingly prevalent disease. In this review, we describe the lipotoxicity effects of the mutant protein in both hepatocytes and hepatic stellate cells (HSCs), driven by its weak triglyceride-hydrolysing activity, altered lipid composition, and resistance to ubiquitin-proteasomal degradation. In the context of MASLD-associated oxidative stress, lipid retention and peroxidation lead to mitochondrial dysfunction, ER stress, and ferroptosis in hepatocytes, while promoting HSC activation and fibrogenesis, thus driving the pathological transition from benign steatosis to MASH. We also summarize mechanism-based therapeutic strategies aimed at supporting the development of personalised, targeted interventions for I148M carriers.

Biomedicine & PharmacotherapyVol. 202
National Clinical Research Center for Digestive Diseases (CN), Community Health Center (US), Beijing Friendship Hospital (CN), Beijing Chaoyang Emergency Medical Center (CN)
National Natural Science Foundation of China, Beijing Nova Program, Capital Health Research and Development of Special Fund
Good health and well-being
Openalex Percentile: Top 9%
Liver Disease Diagnosis and Treatment
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