» Articles » PMID: 35844605

Shaping Polarization Of Tumor-Associated Macrophages In Cancer Immunotherapy

Overview
Journal Front Immunol
Date 2022 Jul 18
PMID 35844605
Authors
Affiliations
Soon will be listed here.
Abstract

Different stimuli can polarize macrophages into two basic types, M1 and M2. Tumor-associated macrophages (TAMs) in the tumor microenvironment (TME) are composed of heterogeneous subpopulations, which include the M1 anti-tumor and M2 pro-tumor phenotypes. TAMs predominantly play a M2-like tumor-promoting role in the TME and regulate various malignant effects, such as angiogenesis, immune suppression, and tumor metastasis; hence, TAMs have emerged as a hot topic of research in cancer therapy. This review focuses on three main aspects of TAMs. First, we summarize macrophage polarization along with the effects on the TME. Second, recent advances and challenges in cancer treatment and the role of M2-like TAMs in immune checkpoint blockade and CAR-T cell therapy are emphasized. Finally, factors, such as signaling pathways, associated with TAM polarization and potential strategies for targeting TAM repolarization to the M1 pro-inflammatory phenotype for cancer therapy are discussed.

Citing Articles

The role of tumor-associated macrophages in lung cancer.

Zhu R, Huang J, Qian F Front Immunol. 2025; 16:1556209.

PMID: 40079009 PMC: 11897577. DOI: 10.3389/fimmu.2025.1556209.


Bacterial-Mediated In Situ Engineering of Tumour-Associated Macrophages for Cancer Immunotherapy.

Kuhl G, Tangney M Cancers (Basel). 2025; 17(5).

PMID: 40075571 PMC: 11899205. DOI: 10.3390/cancers17050723.


Integrated multiomics analysis and machine learning refine neutrophil extracellular trap-related molecular subtypes and prognostic models for acute myeloid leukemia.

Zhong F, Yao F, Wang Z, Liu J, Huang B, Wang X Front Immunol. 2025; 16:1558496.

PMID: 40066454 PMC: 11891243. DOI: 10.3389/fimmu.2025.1558496.


Comprehensive immunophenotyping reveals distinct tumor microenvironment alterations in anti-PD-1 sensitive and resistant syngeneic mouse model.

Inoue H, Hamasaki T, Inoue K, Nakao A, Ebi N, Minomo H Sci Rep. 2025; 15(1):8311.

PMID: 40064915 PMC: 11894063. DOI: 10.1038/s41598-025-91979-w.


Unmasking the potential: mechanisms of neuroinflammatory modulation by oncolytic viruses in glioblastoma.

Beder N, Mirbahari S, Belkhelfa M, Mahdizadeh H, Totonchi M Explor Target Antitumor Ther. 2025; 6:1002294.

PMID: 40061139 PMC: 11886384. DOI: 10.37349/etat.2025.1002294.


References
1.
Jia X, Yu F, Wang J, Iwanowycz S, Saaoud F, Wang Y . Emodin suppresses pulmonary metastasis of breast cancer accompanied with decreased macrophage recruitment and M2 polarization in the lungs. Breast Cancer Res Treat. 2014; 148(2):291-302. PMC: 4224983. DOI: 10.1007/s10549-014-3164-7. View

2.
Xiao M, Zhang J, Chen W, Chen W . M1-like tumor-associated macrophages activated by exosome-transferred THBS1 promote malignant migration in oral squamous cell carcinoma. J Exp Clin Cancer Res. 2018; 37(1):143. PMC: 6038304. DOI: 10.1186/s13046-018-0815-2. View

3.
Sa J, Chang N, Lee H, Cho H, Ceccarelli M, Cerulo L . Transcriptional regulatory networks of tumor-associated macrophages that drive malignancy in mesenchymal glioblastoma. Genome Biol. 2020; 21(1):216. PMC: 7448990. DOI: 10.1186/s13059-020-02140-x. View

4.
Fang W, Zhou T, Shi H, Yao M, Zhang D, Qian H . Progranulin induces immune escape in breast cancer via up-regulating PD-L1 expression on tumor-associated macrophages (TAMs) and promoting CD8 T cell exclusion. J Exp Clin Cancer Res. 2021; 40(1):4. PMC: 7780622. DOI: 10.1186/s13046-020-01786-6. View

5.
Zhu M, Liu W, Wang H, Wang W, Liu N, Lu Y . NSE from diffuse large B-cell lymphoma cells regulates macrophage polarization. Cancer Manag Res. 2019; 11:4577-4595. PMC: 6529732. DOI: 10.2147/CMAR.S203010. View