Evidence map›Paper›PMID 40828155›Full record

ArticleCancer immunology research2025

Tissue-Specific Immunosuppressive and Proliferating Macrophages Fuel Early Metastatic Progression of Human Colorectal Cancer to the Liver.

Paolo Marzano, Cristiana Soldani, Valentina Cazzetta, Barbara Franceschini, Sara Terzoli, Anna Carletti, Michela Anna Polidoro, Federica Marchesi, Massimo Locati, Gianluca Basso and 10 more

Abstract read
In one paragraph

Article in Cancer immunology research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  3. Article
  4. Review
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  7. Association of intratumoral CD68Frontiers in immunology · 2026
    Article
  8. Review
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

20 authors.

Paolo MarzanoDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.ORCID 0000-0002-5614-4033
Cristiana SoldaniLaboratory of Hepatobiliary Immunopathology, IRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0001-5041-9588
Valentina CazzettaUnit of Clinical and Experimental Immunology, IRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0001-7183-2793
Barbara FranceschiniLaboratory of Hepatobiliary Immunopathology, IRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0001-6348-248X
Sara TerzoliUnit of Clinical and Experimental Immunology, IRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0003-2650-7195
Anna CarlettiUnit of Clinical and Experimental Immunology, IRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0003-4468-2499
Michela Anna PolidoroLaboratory of Hepatobiliary Immunopathology, IRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0002-9162-6855
Federica MarchesiDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.ORCID 0000-0002-7212-5721
Massimo LocatiDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.ORCID 0000-0003-3077-590X
Gianluca BassoGenomic Unit, IRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0002-8430-4727
Ana LleoLaboratory of Hepatobiliary Immunopathology, IRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0002-0561-7902
Guido CostaDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.ORCID 0000-0003-3986-8790
Guido TorzilliDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.ORCID 0000-0001-5798-5021
Flavio MilanaDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.ORCID 0000-0003-3570-9573
Rocco PiazzaDepartment of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy.ORCID 0000-0003-4198-9620
Paola SpaggiariDepartment of Pathology, IRCCS Humanitas Research Hospital, Milano, Italy.ORCID 0000-0003-2905-1736
Luca Di TommasoDepartment of Biomedical Sciences, Humanitas University, Milan, Italy.ORCID 0000-0002-9013-4728
Joanna Mikulak *Unit of Clinical and Experimental Immunology, IRCCS Humanitas Research Hospital, Milan, Italy.ORCID 0000-0001-8310-9543
Domenico Mavilio *Department of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.ORCID 0000-0001-6147-0952
Matteo Donadon *Department of Health Sciences, Università del Piemonte Orientale, Novara, Italy.ORCID 0000-0003-0296-7648

Funding

Ministero della Salute (Italy Ministry of Health) RF2018-12367150
6 · The paper itself

Abstract

Early synchronous colorectal liver metastasis (CRLM) represents a clinical condition characterized by the simultaneous presence of primary colorectal cancer and metastatic liver lesions. In this study, we characterized the tissue-specific transcriptomes, phenotypes, and functional relevance of tumor-associated macrophages (TAM) within the tumor microenvironment (TME) of colorectal cancer and CRLM specimens from patients who underwent simultaneous surgical removal of these malignancies. The high-throughput single-cell transcriptional analysis revealed an inverse ratio of inflammatory and immunoregulatory TAMs in the colorectal cancer and CRLM TMEs, along with heterogeneity in both tumoral tissues. Furthermore, we found that inflammatory TAMs in colorectal cancer expressed inhibitory ligands that might support immune escape, thus favoring liver metastatic progression. In contrast, CRLM lesions possessed a highly immunosuppressive milieu characterized by large proliferative CTLA4+ immunoregulatory TAMs and the presence of IL7R+ cytotoxic TAMs. Higher frequencies of these specific TAM subsets in CRLM were associated with shorter disease-free survival and worse patient prognosis. The identification and characterization of immunoregulatory TAMs preferentially enriched in CRLM is key for the development of novel immunotherapeutic strategies aimed at boosting anticancer immune responses within the TME.

Indexed as

Colorectal NeoplasmsLiver NeoplasmsMacrophagesTumor-Associated MacrophagesAgedCell ProliferationDisease ProgressionFemaleHumansMaleMiddle AgedPrognosisTumor Microenvironment

Identifiers

PMID40828155
PMCPMC12580778

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.