Prognostic value of CD163+ macrophages in solid tumor malignancies: A scoping review
- PMID: 39778658
- DOI: 10.1016/j.imlet.2025.106970
Prognostic value of CD163+ macrophages in solid tumor malignancies: A scoping review
Abstract
Tumor-associated macrophages (TAMs) play crucial roles in development and progression of malignant diseases. Notably, CD163+ TAMs likely perform specific pro-tumorigenic functions, suggesting that this subset may serve as both prognostic biomarkers and targets for future anti-cancer therapy. We conducted a scoping review to map the current knowledge on the prognostic role of CD163+ TAMs in the five most lethal cancers worldwide: Lung, colorectal, gastric, liver, and breast cancer. For all cancer types, most studies showed that high tumoral presence of CD163+ cells was associated with poor patient outcome, and this association was more frequently observed when CD163+ cells were measured at the tumor periphery compared to more central parts of the tumor. These results support that CD163+ TAMs represent a biomarker of poor patient outcome across a variety of solid tumors, and highlight the relevance of further investigations of CD163+ TAMs as targets of future immunotherapies.
Keywords: CD163; Cancer; Patient prognosis; Solid tumor malignancy; Targeted immunotherapy; Tumor-associated macrophage.
Copyright © 2025 The Author(s). Published by Elsevier B.V. All rights reserved.
Conflict of interest statement
Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Morten Nørgaard Andersen reports financial support was provided by Novo Nordisk Foundation. Morten Nørgaard Andersen reports financial support was provided by Independent Research Fund Denmark. Kristian Juul-Madsen reports financial support was provided by Independent Research Fund Denmark. Henriette Mathiesen reports financial support was provided by Danish Cancer Society. Morten Nørgaard Andersen reports financial support was provided by Health Research Foundation of Central Denmark Region. Kristian Juul-Madsen reports financial support was provided by Lundbeck Foundation. Anders Etzerodt reports a relationship with Spica Therapeutics that includes: board membership, employment, and equity or stocks. Holger Jon Møller reports a relationship with Spica Therapeutics that includes: equity or stocks. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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