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Updated: Jan 5, 2026

In Vitro Assay to Study Tumor-macrophage Interaction
Published on: August 1, 2019
Tumor-associated macrophages: an accomplice in solid tumor progression
Yibing Chen1, Yucen Song2, Wei Du3
1Genetic and Prenatal Diagnosis Center, Department of Gynecology and Obstetrics, First Affiliated Hospital, Zhengzhou University, 1 Jianshe Road East, Zhengzhou, 450052, Henan, China. chenyibing@zzu.edu.cn.
Abstract:
In many solid tumor types, tumor-associated macrophages (TAMs) are important components of the tumor microenvironment (TME). Moreover, TAMs infiltration is strongly associated with poor survival in solid tumor patients. In this review, we describe the origins of TAMs and their polarization state dictated by the TME. We also specifically focus on the role of TAMs in promoting tumor growth, enhancing cancer cells resistance to chemotherapy and radiotherapy, promoting tumor angiogenesis, inducing tumor migration and invasion and metastasis, activating immunosuppression. In addition, we discuss TAMs can be used as therapeutic targets of solid tumor in clinics. The therapeutic strategies include clearing macrophages and inhibiting the activation of TAMs, promoting macrophage phagocytic activity, limiting monocyte recruitment and other targeted TAMs therapies.
Insights
Tumor-associated macrophages (TAMs) drive solid tumor progression and resistance to cancer therapies. Targeting TAMs offers a promising therapeutic strategy for improving patient survival in solid tumors.
Area of Science:
- Oncology
- Immunology
- Cancer Biology
Background:
- Tumor-associated macrophages (TAMs) are key players in the tumor microenvironment (TME) of many solid tumors.
- TAM infiltration correlates with poorer patient survival across various solid tumor types.
Purpose of the Study:
- To review the origins and polarization of TAMs within the TME.
- To elucidate the multifaceted roles of TAMs in promoting tumor growth, therapeutic resistance, angiogenesis, invasion, metastasis, and immunosuppression.
- To discuss TAMs as viable therapeutic targets in clinical settings.
Main Methods:
- Literature review focusing on the biology and clinical relevance of TAMs.
- Analysis of TAM functions including promotion of tumor growth, treatment resistance, angiogenesis, and metastasis.
- Exploration of therapeutic strategies targeting TAMs.
Main Results:
- TAMs originate from monocytes and adopt polarization states influenced by the TME.
- TAMs actively promote tumor progression through various mechanisms, including enhancing chemo- and radioresistance.
- TAMs play a critical role in tumor angiogenesis, migration, invasion, metastasis, and immune suppression.
Conclusions:
- TAMs are crucial mediators of solid tumor progression and therapeutic resistance.
- Targeting TAMs, through strategies like macrophage depletion or activation modulation, presents a promising avenue for cancer therapy.
- Further research into TAM-targeted therapies could significantly improve outcomes for solid tumor patients.
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