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. 2023 Aug 19;7:78. doi: 10.1038/s41698-023-00431-7

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — TAM mainly originates from microglia in the brain and peripheral-derived monocytes, and its activation types contribute to a suppressive immune microenvironment and thus results in various tumor biological behavior. As a result, TAM-targeted therapy mainly targets its recruitment, polarization, and its multiple function in tumor behavior. TAM tumor-associated macrophage, CCL chemokine ligand, CYP cytochrome P450, CSF colony-stimulating factor, VEGF vascular endothelial growth factor, HIF-1 hypoxia-inducible factors-1 (Created with BioRender.com).