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Updated: May 13, 2026

In Vitro Assay to Study Tumor-macrophage Interaction
Published on: August 1, 2019
MicroRNA-mediated control of macrophages and its implications for cancer
Mario Leonardo Squadrito1, Martin Etzrodt, Michele De Palma
1The Swiss Institute for Experimental Cancer Research (ISREC), School of Life Sciences, Swiss Federal Institute of Technology Lausanne (EPFL), 1015 Lausanne, Switzerland.
Abstract:
Deregulation of microRNAs (miRNAs) can drive oncogenesis, tumor progression, and metastasis by acting cell-autonomously in cancer cells. However, solid tumors are also infiltrated by large amounts of non-neoplastic stromal cells, including macrophages, which express several active miRNAs. Tumor-associated macrophages (TAMs) enhance angiogenic, immunosuppressive, invasive, and metastatic programming of neoplastic tissue and reduce host survival. Here, we review the role of miRNAs (including miR-155, miR-146, and miR-511) in the control of macrophage production and activation, and examine whether reprogramming miRNA activity in TAMs and/or their precursors might be effective for controlling tumor progression.
Insights
MicroRNAs (miRNAs) are key in cancer progression. This review explores how targeting miRNAs in tumor-associated macrophages (TAMs) could offer new cancer treatment strategies by controlling tumor growth and spread.
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- MicroRNA (miRNA) deregulation drives cancer development, progression, and metastasis within cancer cells.
- Solid tumors contain non-neoplastic stromal cells, notably tumor-associated macrophages (TAMs), which express active miRNAs.
- TAMs promote tumor angiogenesis, immunosuppression, invasion, and metastasis, ultimately reducing patient survival.
Purpose of the Study:
- To review the critical role of specific miRNAs (e.g., miR-155, miR-146, miR-511) in regulating macrophage production and activation.
- To investigate the potential of reprogramming miRNA activity in TAMs and their precursors as a therapeutic strategy against cancer progression.
Main Methods:
- Literature review of studies on miRNA function in cancer and macrophages.
- Analysis of the impact of specific miRNAs on macrophage biology within the tumor microenvironment.
- Examination of preclinical and clinical data regarding miRNA-targeted therapies in cancer.
Main Results:
- Certain miRNAs are integral to the control of macrophage differentiation and activation states.
- miRNA dysregulation in TAMs contributes significantly to the pro-tumorigenic functions of the tumor microenvironment.
- Targeting specific miRNAs in TAMs shows promise in preclinical models for inhibiting tumor growth and metastasis.
Conclusions:
- miRNAs play a dual role in cancer, both within neoplastic cells and in the tumor microenvironment via TAMs.
- Modulating miRNA activity in TAMs represents a promising, yet underexplored, therapeutic avenue for cancer treatment.
- Further research into miRNA-based strategies targeting TAMs is warranted to develop novel anti-cancer therapies.
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