Evidence map›Paper›PMID 42811675›Full record

ArticleJournal of immunology research2026

Spatial Profiling and Prognostic Role of CD169+ Macrophages in Colorectal Cancer From Adjacent Nontumor Mucosa to Liver Metastasis.

Wenjing Ye, Sergii Pavlov, Esraa Ali, Filip Ambrozkiewicz, Lenka Červenková, Ondřej Vyčítal, Petr Hošek, Ondřej Daum, Václav Liška, Kari Hemminki and 1 more

Abstract read
In one paragraph

Article in Journal of immunology research, 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

11 authors.

Wenjing YeLaboratory of Translational Cancer Genomics, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 1665/76, 32300, Pilsen, Czech Republic, cuni.cz.ORCID https://orcid.org/0009-0004-3293-0437
Sergii PavlovLaboratory of Translational Cancer Genomics, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 1665/76, 32300, Pilsen, Czech Republic, cuni.cz.
Esraa AliLaboratory of Translational Cancer Genomics, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 1665/76, 32300, Pilsen, Czech Republic, cuni.cz.ORCID https://orcid.org/0000-0002-8418-6716
Filip AmbrozkiewiczLaboratory of Translational Cancer Genomics, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 1665/76, 32300, Pilsen, Czech Republic, cuni.cz.ORCID https://orcid.org/0000-0001-6850-780X
Lenka ČervenkováLaboratory of Cancer Treatment and Tissue Regeneration, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 1665/76, 32300, Pilsen, Czech Republic, cuni.cz.ORCID https://orcid.org/0000-0001-7251-210X
Ondřej VyčítalLaboratory of Cancer Treatment and Tissue Regeneration, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 1665/76, 32300, Pilsen, Czech Republic, cuni.cz.
Petr HošekLaboratory of Cancer Treatment and Tissue Regeneration, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 1665/76, 32300, Pilsen, Czech Republic, cuni.cz.
Ondřej DaumLaboratory of Cancer Treatment and Tissue Regeneration, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 1665/76, 32300, Pilsen, Czech Republic, cuni.cz.ORCID https://orcid.org/0000-0002-0930-7071
Václav LiškaLaboratory of Cancer Treatment and Tissue Regeneration, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 1665/76, 32300, Pilsen, Czech Republic, cuni.cz.
Kari HemminkiLaboratory of Translational Cancer Genomics, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 1665/76, 32300, Pilsen, Czech Republic, cuni.cz.
Andriy TrailinLaboratory of Translational Cancer Genomics, Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Alej Svobody 1665/76, 32300, Pilsen, Czech Republic, cuni.cz.ORCID https://orcid.org/0000-0001-8888-0759

Funding

Cooperation Program, Research Area SURG, the Integration of Biomedical Research and Health Care in the Pilsen Metropolitan AreaEuropean Union and by the State Budget of the Czech Republic CZ.02.01.01/00/23_021/0008828Ministerstvo Zdravotnictví Ceské Republiky AZV NU21-03-00506Ministerstvo Zdravotnictví Ceské Republiky AZV NW24-03-00521
6 · The paper itself

Abstract

backgroundCD169+ cells represent a distinct subset of macrophages with potential immunomodulatory roles, but their function in colorectal cancer (CRC) progression remains unclear. This study focuses on the spatial profiling and prognostic significance of CD169+ macrophages in adjacent nontumor mucosa (NM), primary CRC (pCRC), and synchronous or metachronous liver metastases (LM). MATERIALS AND

methodsWe enrolled into this retrospective cohort study patients who underwent resection of both pCRC with adjacent NM and synchronous LM (N = 55) or metachronous LM (N = 44). We applied immunohistochemical staining and computer-assisted image analysis to quantify CD169+ cell density in the NM, pCRC, synchronous, and metachronous LM. Correlations between CD169+ macrophages and T cells were evaluated. Associations between CD169+ cell density and overall survival (OS) of the patients were assessed.

resultsCD169+ cell density was greater in NM than in the tumor center (TC) of pCRC and in the peritumor (PT) region of LM compared to pCRC. The synchronous group exhibited a higher density of CD169+ cells than the metachronous group in the inner margin (IM) of pCRC, the TC, and the outer margin (OM) of LM. CD169+ cells were more abundant in the exterior than in the interior tumor areas in both pCRC and LM. Positive correlations were observed between densities of CD169+ macrophages with CD3+ and CD8+ lymphocytes. In the synchronous group, a high density of CD169+ macrophages in the TC of pCRC was associated with longer OS, whereas a high density in the PT of LM was associated with shorter OS. High density of CD169+ macrophages in the OM of metachronous LM was associated with poor survival.

conclusionOur study highlights context-dependent prognostic associations of CD169+ macrophages in CRC. While high CD169+ macrophage density in the TC of pCRC was linked to favorable survival in the synchronous group, increased density in both synchronous and metachronous LM was associated with adverse outcomes. Further prospective studies and functional investigations are needed to validate these observations.

Indexed as

Colorectal NeoplasmsIntestinal MucosaLiver NeoplasmsMacrophagesSialic Acid Binding Ig-like Lectin 1AdultAgedBiomarkers, TumorFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesBiomarkers, TumorSialic Acid Binding Ig-like Lectin 1SIGLEC1 protein, humanCD169colorectal cancerliver metastasesmacrophagesmetachronoussurvival analysissynchronous

Identifiers

PMID42811675
PMCPMC13624539

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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.