Evidence map›Paper›PMID 42835662›Full record

ReviewFrontiers in pharmacology2026

Lipid metabolism as a cell-state determinant in pulmonary fibrosis: from epithelial failure to ferroptosis-driven amplification.

Er Lin, Zhehua Shao, Jiahao Liu, Zihan Yi, Lanying Shen, Yinghua Ying, Yue Hu

Abstract readReview
In one paragraph

Review in Frontiers in pharmacology, 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

7 authors.

Er Lin *Key Laboratory of Respiratory Disease of Zhejiang Province, Department of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Zhehua Shao *Key Laboratory of Respiratory Disease of Zhejiang Province, Department of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Jiahao LiuKey Laboratory of Respiratory Disease of Zhejiang Province, Department of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Zihan YiKey Laboratory of Respiratory Disease of Zhejiang Province, Department of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Lanying ShenKey Laboratory of Respiratory Disease of Zhejiang Province, Department of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Yinghua YingKey Laboratory of Respiratory Disease of Zhejiang Province, Department of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Yue HuKey Laboratory of Respiratory Disease of Zhejiang Province, Department of Respiratory and Critical Care Medicine, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite 2 decades of mechanistic progress, pulmonary fibrosis still progresses in many patients, and established scar rarely resolves. Lipid metabolism has emerged as a unifying lens on this disease, but a useful synthesis requires recognizing that the relevant abnormalities are compartment-specific, stage-dependent, and unevenly supported by human evidence. Here we argue that lipid metabolism in pulmonary fibrosis is best understood as a determinant of cell-state stability, and that its failure plays out differently across three compartments. In alveolar epithelial cells, reduced lipogenesis, impaired fatty-acid oxidation, surfactant imbalance, and lipotoxic stress destabilize the regenerative AT2 state. This compartment exhibits the most consistent correlative human tissue associations reported to date. In fibroblasts, a shift away from fatty-acid oxidation toward anabolic and lipogenic programs likely stabilizes cells into a persistent myofibroblast identity at the expense of more reparative lipofibroblast-like states. In macrophages, altered lipid uptake, oxidized-lipid responses, and disturbed cholesterol handling support a profibrotic niche, with ontogeny and metabolic profile increasingly displacing classical M1/M2 categories. These compartment-specific programs converge on a shared downstream amplifier, namely phospholipid peroxidation and ferroptosis, where the strongest evidence again concerns injured epithelium. Therapeutic strategies group naturally into three tiers: clinical anchors with indirect metabolic relevance, including pirfenidone, nintedanib, and PDE4B inhibition; repurposed agents with metabolic rationale, including metformin, ezetimibe, and PPAR and LXR modulators; and mechanism-driven, largely preclinical strategies targeting mitochondrial-redox balance and ferroptosis. Reframing lipid metabolism as a cell-state determinant clarifies which abnormalities are actionable, in which compartments they matter, and when intervention is most likely to alter disease course.

Indexed as

alveolar epithelial cellsfatty-acid oxidationferroptosisfibroblastslipid metabolismlipid peroxidationmacrophagespulmonary fibrosis

Identifiers

PMID42835662
PMCPMC13635660

What OpenQuestion holds

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Registered trials

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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.