Evidence map›Paper›PMID 42882471›Full record

ArticleCells2026

Distinct OA:PA Ratios Generate Discrete Hepatocellular Phenotypes in HepG2 Cells.

Hangyeon Jeong, Yesol Han, Jiyeong Park, Hanbyul Noh, Eunyoung Moon, Yanghoon Huh

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Hangyeon JeongCenter for Bio-Imaging & Translational Research, Korea Basic Science Institute, Cheongju 28119, Republic of Korea.ORCID 0000-0001-5429-9181
Yesol HanCenter for Bio-Imaging & Translational Research, Korea Basic Science Institute, Cheongju 28119, Republic of Korea.
Jiyeong ParkCenter for Bio-Imaging & Translational Research, Korea Basic Science Institute, Cheongju 28119, Republic of Korea.ORCID 0009-0006-2207-2189
Hanbyul NohCenter for Bio-Imaging & Translational Research, Korea Basic Science Institute, Cheongju 28119, Republic of Korea.
Eunyoung MoonCenter for Bio-Imaging & Translational Research, Korea Basic Science Institute, Cheongju 28119, Republic of Korea.ORCID 0000-0002-6632-8071
Yanghoon HuhCenter for Bio-Imaging & Translational Research, Korea Basic Science Institute, Cheongju 28119, Republic of Korea.

Funding

Korea Basic Science Institute C612101Korea Basic Science Institute C623200National Research Foundation RS-2022-NR068424
6 · The paper itself

Abstract

Metabolic dysfunction-associated steatohepatitis (MASH) is characterized by hepatic steatosis, metabolic stress, and inflammation. Although free fatty acid (FFA)-based in vitro models are widely used, how OA:PA ratios shape hepatocellular phenotypes remains incompletely characterized. HepG2 cells were treated with oleic acid (OA), palmitic acid (PA), or four OA:PA mixtures (O1P1, O2P1, O3P2, O1P2) for 24 or 48 h. OA and OA:PA mixtures were evaluated at 500 μM total FFA (O2P1: 333.3 μM OA + 166.7 μM PA; O3P2: 300 μM OA + 200 μM PA), whereas PA alone was evaluated at 200 μM. Cell viability, lipid accumulation, ultrastructure, oxidative response, secreted cytokines, and molecular responses were evaluated. Distinct OA:PA ratios generated discrete hepatocellular states rather than a linear steatosis-to-lipotoxicity continuum. O3P2 produced a steatosis-dominant phenotype with pronounced lipid accumulation and relatively limited stress signaling. In contrast, O2P1 combined substantial lipid accumulation with elevated DCF fluorescence, AMP-activated protein kinase (AMPK) phosphorylation, nuclear factor kappa B (NF-κB)-associated inflammatory signaling, and interleukin-8 (IL-8) secretion, representing a pronounced stress-responsive phenotype with selected MASH-relevant features. Selected responses were also evaluated in SNU-449 cells, revealing cell-line-specific patterns. Collectively, these findings support a phenotype-oriented framework for OA:PA ratio selection in hepatocyte-based in vitro MASH modeling.

Indexed as

HepatocytesOleic AcidPalmitic AcidAMP-Activated Protein KinasesCell SurvivalFatty LiverHep G2 CellsHumansLipid MetabolismOxidative StressPhenotypeReactive Oxygen SpeciesAMP-Activated Protein KinasesOleic AcidPalmitic AcidReactive Oxygen Speciesfatty acid ratiohepatocellular phenotypeHepG2 cellslipid dropletlipotoxic stressoleic acidpalmitic acidsteatosis

Identifiers

PMID42882471
PMCPMC13664436

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.