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The PNPLA3 I148M variant is a key genetic determinant of metabolic dysfunction-associated steatotic liver disease (MASLD) and related conditions, contributing to lipid metabolism dysregulation and disease progression. To identify small molecules that modulate PNPLA3 I148M, we conducted a high-content screen of over 820,000 compounds and identified NUV-244, a potent degrader of PNPLA3 I148M in liver-derived cells. NUV-244 reduces PNPLA3 I148M levels on lipid droplets via the ubiquitin-proteasome system, involving the E3 ligase BFAR, without affecting PNPLA2. It restores lipid droplet morphology and improves cellular fitness in PNPLA3 I148M-expressing cells. These findings provide a tool to investigate PNPLA3 I148M function and offer a potential strategy for developing targeted therapies for MASLD and related diseases. By enabling selective degradation of PNPLA3 I148M, this approach expands therapeutic possibilities beyond genetic manipulation, addressing a critical need in metabolic liver disease research.
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Patrick Steigemann
Nuvisan (Germany)
Nico Braeuer
Nuvisan (Germany)
Vera Puetter
Nuvisan (Germany)
iScience
University of Gothenburg
Nuvisan (Germany)
Foresite (United States)
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Steigemann et al. (Tue,) studied this question.
synapsesocial.com/papers/6a099b7f0e219f8cdd3427ce — DOI: https://doi.org/10.1016/j.isci.2025.112384