Tumor-Associated Macrophages as Major Immunosuppressive Cells in the Tumor Microenvironment

Author:

Ghebremedhin Anghesom1,Athavale Dipti1,Zhang Yanting12,Yao Xiaodan1,Balch Curt12,Song Shumei1234ORCID

Affiliation:

1. Coriell Institute for Medical Research, 403 Haddon Ave., Camden, NJ 08103, USA

2. Department Biomedical Sciences, Cooper Medical School of Rowan University, 401 Broadway, Camden, NJ 08103, USA

3. MD Anderson Cancer Center at Cooper, Cooper University Hospital, 2 Cooper Plaza, Camden, NJ 08103, USA

4. Departments of Surgery, Cooper University Hospital, 1 Cooper Plaza, Camden, NJ 08103, USA

Abstract

Within the tumor microenvironment, myeloid cells constitute a dynamic immune population characterized by a heterogeneous phenotype and diverse functional activities. In this review, we consider recent literature shedding light on the increasingly complex biology of M2-like immunosuppressive tumor-associated macrophages (TAMs), including their contribution to tumor cell invasion and metastasis, stromal remodeling (fibrosis and matrix degradation), and immune suppressive functions, in the tumor microenvironment (TME). This review also delves into the intricate signaling mechanisms underlying the polarization of diverse macrophage phenotypes, and their plasticity. We also review the development of promising therapeutic approaches to target these populations in cancers. The expanding knowledge of distinct subsets of immunosuppressive TAMs, and their contributions to tumorigenesis and metastasis, has sparked significant interest among researchers regarding the therapeutic potential of TAM depletion or phenotypic modulation.

Funder

Department of Defense

National Institutes of Health

New Jersey Health Foundation

Publisher

MDPI AG

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