Open Access
REVIEW
The heterogeneity of tumor-associated macrophages and strategies to target it
HAO LV1, BO ZHU1,2, DEGAO CHEN1,2,*
1 Institute of Cancer, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China
2 Chongqing Key Laboratory of Immunotherapy, Xinqiao Hospital, Third Military Medical University, Chongqing, 400037, China
* Corresponding Author: DEGAO CHEN. Email:
(This article belongs to the Special Issue: Macrophages in Cancer Therapy)
BIOCELL 2024, 48(3), 363-378. https://doi.org/10.32604/biocell.2023.046367
Received 27 September 2023; Accepted 30 November 2023; Issue published 15 March 2024
Abstract
Tumor-associated macrophages (TAMs) are emerging as targets for tumor therapy because of their primary role in promoting tumor progression. Several studies have been conducted to target TAMs by reducing their infiltration, depleting their numbers, and reversing their phenotypes to suppress tumor progression, leading to the development of drugs in preclinical and clinical trials. However, the heterogeneous characteristics of TAMs, including their ontogenetic and functional heterogeneity, limit their targeting. Therefore, in-depth exploration of the heterogeneity of TAMs, combined with immune checkpoint therapy or other therapeutic modalities could improve the efficiency of tumor treatment. This review focuses on the heterogeneous ontogeny and function of TAMs, as well as the current development of tumor therapies targeting TAMs and combination strategies.
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APA Style
LV, H., ZHU, B., CHEN, D. (2024). The heterogeneity of tumor-associated macrophages and strategies to target it. BIOCELL, 48(3), 363-378. https://doi.org/10.32604/biocell.2023.046367
Vancouver Style
LV H, ZHU B, CHEN D. The heterogeneity of tumor-associated macrophages and strategies to target it. BIOCELL . 2024;48(3):363-378 https://doi.org/10.32604/biocell.2023.046367
IEEE Style
H. LV, B. ZHU, and D. CHEN "The heterogeneity of tumor-associated macrophages and strategies to target it," BIOCELL , vol. 48, no. 3, pp. 363-378. 2024. https://doi.org/10.32604/biocell.2023.046367