Evidence map›Paper›PMID 32907830›Full record

ArticleGut2021

TREM-2 defends the liver against hepatocellular carcinoma through multifactorial protective mechanisms.

Aitor Esparza-Baquer, Ibone Labiano, Omar Sharif, Aloña Agirre-Lizaso, Fiona Oakley, Pedro M Rodrigues, Ekaterina Zhuravleva, Colm J O'Rourke, Elizabeth Hijona, Raul Jimenez-Agüero and 16 more

Open access · hybridAbstract read
In one paragraph

Article in Gut, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
4.9field-weighted citation impact, top 4% of its field
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

73 citing papers in PubMed, 114 citations in OpenAlex.

  1. Article
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  4. Review
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  6. PMAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  7. Review
  8. [Heterogeneity of tumor-associated macrophages and precision targeting strategies in hepatocellular carcinoma].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2026
    Review
  9. Paclitaxel drives TREM2Nature communications · 2026
    Article
  10. Article
  11. Review
  12. TREM2-expressing macrophages in liver diseases.Trends in endocrinology and metabolism: TEM · 2026
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Molecular mechanisms in MASLD/MASH-related HCC.Hepatology (Baltimore, Md.) · 2025
    Review
  19. Lipid-Metabolically Active TREM2Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
    Article
  20. Review

13 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 8 institutions in 5 countries.

Aitor Esparza-BaquerDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain.
Ibone LabianoDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain.
Omar SharifInstitute for Vascular Biology, Center for Physiology and Pharmacology, Medical University Vienna, Vienna, Austria.
Aloña Agirre-LizasoDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain.
Fiona OakleyNewcastle Fibrosis Research Group, Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
Pedro M RodriguesDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain.
Ekaterina ZhuravlevaDepartment of Health and Medical Sciences, Biotech Research & Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.
Colm J O'RourkeDepartment of Health and Medical Sciences, Biotech Research & Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.
Elizabeth HijonaDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain.
Raul Jimenez-AgüeroDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain.
Ioana RiañoDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain.
Ana LandaDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain.
Adelaida La CastaDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain.
Marco Y W ZakiNewcastle Fibrosis Research Group, Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0003-3097-5776
Patricia Munoz-GarridoDepartment of Health and Medical Sciences, Biotech Research & Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.
Mikel AzkargortaCIBERehd, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Felix ElortzaCIBERehd, Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
Andrea VogelInstitute for Vascular Biology, Center for Physiology and Pharmacology, Medical University Vienna, Vienna, Austria.ORCID 0000-0002-2613-140X
Gernot SchabbauerInstitute for Vascular Biology, Center for Physiology and Pharmacology, Medical University Vienna, Vienna, Austria.
Patricia AspichuetaDepartment of Physiology, Faculty of Medicine and Nursing, University of the Basque Country, UPV/EHU, Lejona, Spain.
Jesper B AndersenDepartment of Health and Medical Sciences, Biotech Research & Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-1760-5244
Sylvia KnappCeMM, Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Derek A MannNewcastle Fibrosis Research Group, Institute of Cellular Medicine, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
Luis BujandaDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain.
Jesus Maria BanalesDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain matxus.perugorria@biodonostia.org jesus.banales@biodonostia.org.ORCID 0000-0002-5224-2373
Maria Jesus PerugorriaDepartment of Liver and Gastrointestinal Diseases, Biodonostia Health Research Institute, Donostia University Hospital, San Sebastian, Spain matxus.perugorria@biodonostia.org jesus.banales@biodonostia.org.ORCID 0000-0002-7636-0972
Biogipuzkoa Health Research Institute · ESInstituto de Salud Carlos III · ESUniversity of Copenhagen · DKChristian Doppler Laboratory for Thermoelectricity · ATNewcastle University · GBIkerbasque · ESUniversity of the Basque Country · ESAustrian Academy of Sciences · AT

Funding

Austrian Science Fund FWF P 31568Cancer Research UK 23390Cancer Research UK 26813Medical Research Council MR/K001949/1Medical Research Council MR/R023026/1
6 · The paper itself

Abstract

objectiveHepatocellular carcinoma (HCC) is a prevalent and aggressive cancer usually arising on a background of chronic liver injury involving inflammatory and hepatic regenerative processes. The triggering receptor expressed on myeloid cells 2 (TREM-2) is predominantly expressed in hepatic non-parenchymal cells and inhibits Toll-like receptor signalling, protecting the liver from various hepatotoxic injuries, yet its role in liver cancer is poorly defined. Here, we investigated the impact of TREM-2 on liver regeneration and hepatocarcinogenesis.

designTREM-2 expression was analysed in liver tissues of two independent cohorts of patients with HCC and compared with control liver samples. Experimental HCC and liver regeneration models in wild type and

results

conclusionTREM-2 plays a protective role in hepatocarcinogenesis via different pleiotropic effects, suggesting that TREM-2 agonism should be investigated as it might beneficially impact HCC pathogenesis in a multifactorial manner.

Indexed as

AdultAgedAnimalsCarcinogenesisCarcinoma, HepatocellularCell Line, TumorCell ProliferationDiethylnitrosamineFemaleGain of Function MutationGene ExpressionHepatic Stellate CellsHepatitisHepatocytesHumansLiverDiethylnitrosamineMembrane GlycoproteinsReactive Oxygen SpeciesReceptors, ImmunologicRNATREM2 protein, humanTrem2 protein, mouseWnt3 ProteinWNT3 protein, humanWNT7A protein, humanWNT8A protein, humanWnt Proteinshepatocellular carcinomaimmune-mediated liver damageliver immunologyliver regenerationmolecular carcinogenesis

Identifiers

PMID32907830
PMCPMC8223629
OpenAlexW3084030626

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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.