Evidence map›Paper›PMID 41351176›Full record

ReviewJournal of translational medicine2025

Foam cells: tracing the diverse cellular origins and their linked signaling pathways.

Xinyun Jiao, Dachuan Guo, Wenlin Li, Sainan Li, Guangying Shao, Tao Shen, Xue Yu

Abstract readReview
In one paragraph

Review in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
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  4. Article
  5. Article
  6. Review
  7. Novel insights of ferroptosis in atherosclerosis progression.Frontiers in cell and developmental biology · 2026
    Review
  8. Review
  9. Review
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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.

Xinyun JiaoDepartment of Cardiology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, China.
Dachuan GuoDepartment of Cardiology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, China.
Wenlin LiThe Key Laboratory of Geriatrics, Beijing Institute of Geriatrics/Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing Hospital, National Center of Gerontology of National Health Commission, Beijing, 100730, China.
Sainan LiDepartment of Cardiology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, China.
Guangying ShaoDepartment of Cardiology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, China.
Tao ShenThe Key Laboratory of Geriatrics, Beijing Institute of Geriatrics/Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing Hospital, National Center of Gerontology of National Health Commission, Beijing, 100730, China. shentao4189@bjhmoh.cn.ORCID 0000-0001-5856-0818
Xue YuDepartment of Cardiology, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100730, China. yuxue2652@bjhmoh.cn.

Funding

Capital's Funds for Health Improvement and Research BJ-2024-1-405High-level Hospital Construction Project of Guangdong Provincial People's Hospital BJ-2025-148, BJ-2024-246 and BJ-2024-219Key Technologies Research and Development Program of Guangzhou Municipality 2023YFC3605800National Natural Science Foundation of China 82470395the Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences 2021-I2M-1-050
6 · The paper itself

Abstract

Foam cells play a crucial role in the formation and progression of atherosclerotic plaque. In addition to classical monocytes and vascular smooth muscle cells (VSMCs), foam cells can also originate from dendritic cells, endothelial cells, and stem cells. VSMCs account for over 75% of foam cells in murine models and approximately 50% in human plaques. Foam cell formation involves dysregulated cholesterol homeostasis, including impaired uptake via scavenger receptors like CD36, impaired efflux via ABCA1/ABCG1, and defective autophagy. Formation is also regulated by multiple signaling pathways, including inflammatory (TLR4-NF-κB and NLRP3 inflammasome), metabolic (PPARγ-LXRα and PI3K/Akt), and microenvironmental (Notch and Wnt) pathways. This review summarizes the cellular origins and regulatory mechanisms of foam cells, providing insights for targeted atherosclerosis therapies.

Indexed as

Cell LineageFoam CellsSignal TransductionAnimalsAtherosclerosisHumansAtherosclerosisFoam cellInflammationMacrophagePhenotype modulation

Identifiers

PMID41351176
PMCPMC12681170

What OpenQuestion holds

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Registered trials

None linked

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.