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Melanoma-derived cytokines and extracellular vesicles are interlinked with macrophage immunosuppression.

Authors :
Suman S
Nevala WK
Leontovich AA
Jakub JW
Geng L
McLaughlin SA
Markovic SN
Source :
Frontiers in molecular biosciences [Front Mol Biosci] 2025 Jan 22; Vol. 11, pp. 1522717. Date of Electronic Publication: 2025 Jan 22 (Print Publication: 2024).
Publication Year :
2025

Abstract

Cytokines play a crucial role in mediating cell communication within the tumor microenvironment (TME). Tumor-associated macrophages are particularly influential in the regulation of immunosuppressive cytokines, thereby supporting tumor metastasis. The upregulation of Th2 cytokines in cancer cells is recognized for its involvement in suppressing anticancer immunity. However, the association between these cytokines and tumor-secreted extracellular vesicles (EVs) remains poorly understood. Therefore, our objective was to investigate the connection between tumor-promoting macrophages and melanoma-derived EVs. The analysis from altered cytokine profile data showed that melanoma-derived EVs upregulate Th2 cytokine expression in naïve macrophages, thereby contributing to the promotion of tumor-supporting functions. Notably, many of these cytokines were also found to be upregulated in metastatic melanoma patients (n = 30) compared to healthy controls (n = 33). Overall, our findings suggest a strong connection between melanoma secretory EVs and the induction of tumor-associated macrophages that facilitates the development of an immunosuppressive TME, supporting melanoma metastasis through regulation at both local and systemic levels.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2025 Suman, Nevala, Leontovich, Jakub, Geng, McLaughlin and Markovic.)

Details

Language :
English
ISSN :
2296-889X
Volume :
11
Database :
MEDLINE
Journal :
Frontiers in molecular biosciences
Publication Type :
Academic Journal
Accession number :
39911494
Full Text :
https://doi.org/10.3389/fmolb.2024.1522717