Evidence map›Paper›PMID 42523651›Full record

ArticleFrontiers in immunology2026

Upregulated FASN-mediated lipogenesis in senescent macrophages contributes to liver fibrosis progression.

Hongliang Dong, Chuanfang Shu, Ran Liu, Mingpei Zhao, Kaiyue Zhang, Ziqun Qu, Lili Wang, Jing Fan, Wei Ye

Abstract read
In one paragraph

Article in Frontiers in immunology, 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

9 authors.

Hongliang DongDepartment of Infectious Disease and Liver Disease, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Chuanfang ShuDepartment of Infectious Disease and Liver Disease, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Ran LiuDepartment of Infectious Disease and Liver Disease, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Mingpei ZhaoDepartment of Infectious Disease and Liver Disease, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Kaiyue ZhangDepartment of Infectious Disease and Liver Disease, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Ziqun QuDepartment of Infectious Disease and Liver Disease, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Lili WangDepartment of Infectious Disease and Liver Disease, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Jing FanDepartment of Infectious Disease and Liver Disease, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Wei YeDepartment of Infectious Disease and Liver Disease, The Second Hospital of Nanjing, Affiliated to Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Liver fibrosis represents a common advanced pathological stage of various chronic liver diseases. Macrophages serve as key regulators of innate immunity and play important roles in the development of liver fibrosis. Cellular senescence is an irreversible cell cycle arrest state. However, the mechanisms underlying the role of senescent macrophages in liver fibrosis remain incompletely understood. Methods: Liver fibrosis was induced in young (8-week) and middle-aged (12-month) mice by intraperitoneal injection of 25% carbon tetrachloride (CCl Results: Conclusion: Macrophages in middle-aged fibrotic livers exhibit cellular senescence. FASN-mediated enhancement of fatty acid synthesis leads to lipid metabolic disorder and accumulation in senescent macrophages. These senescent macrophages promote HSC activation and drive the progression of liver fibrosis.

Indexed as

Cellular SenescenceFatty Acid Synthase, Type ILipogenesisLiver CirrhosisMacrophagesAnimalsCarbon TetrachlorideDisease ProgressionHepatic Stellate CellsHumansMaleMiceMice, Inbred C57BLRAW 264.7 CellsUp-RegulationCarbon TetrachlorideFasn protein, mouseFatty Acid Synthase, Type Icellular senescencefatty acid metabolismhepatic stellate cellsliver fibrosismacrophages

Identifiers

PMID42523651
PMCPMC13407210

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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.