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Updated: Jul 26, 2025

In Vitro Assay to Study Tumor-macrophage Interaction
Published on: August 1, 2019
Tumor hijacks macrophages and microbiota through extracellular vesicles
Jipeng Jiang1,2, Jie Mei3,4, Yongfu Ma2
1Postgraduate School Medical School of Chinese PLA Beijing P. R. China.
Abstract:
The tumor microenvironment (TME) is a biological system with sophisticated constituents. In addition to tumor cells, tumor-associated macrophages (TAMs) and microbiota are also dominant components. The phenotypic and functional changes of TAMs are widely considered to be related to most tumor progressions. The chronic colonization of pathogenic microbes and opportunistic pathogens accounts for the generation and development of tumors. As messengers of cell-to-cell communication, tumor-derived extracellular vesicles (TDEVs) can transfer various malignant factors, regulating physiological and pathological changes in the recipients and affecting TAMs and microbes in the TME. Despite the new insights into tumorigenesis and progress brought by the above factors, the crosstalk among tumor cells, macrophages, and microbiota remain elusive, and few studies have focused on how TDEVs act as an intermediary. We reviewed how tumor cells recruit and domesticate macrophages and microbes through extracellular vehicles and how hijacked macrophages and microbiota interact with tumor-promoting feedback, achieving a reciprocal coexistence under the TME and working together to facilitate tumor progression. It is significant to seek evidence to clarify those specific interactions and reveal therapeutic targets to curb tumor progression and improve prognosis.
Insights
Tumor-derived extracellular vesicles (TDEVs) mediate crosstalk between tumor cells, macrophages, and microbes within the tumor microenvironment (TME). Understanding these interactions is key to developing new cancer therapies.
Area of Science:
- Oncology
- Immunology
- Microbiology
Background:
- The tumor microenvironment (TME) comprises tumor cells, tumor-associated macrophages (TAMs), and microbiota, all influencing tumor progression.
- TAMs' altered phenotypes and functions are linked to cancer development.
- Microbial colonization, including pathogens, contributes to tumor generation and progression.
Purpose of the Study:
- To review the role of tumor-derived extracellular vesicles (TDEVs) in mediating crosstalk among tumor cells, TAMs, and microbiota.
- To elucidate how TDEVs facilitate the recruitment and interaction of TAMs and microbes within the TME.
- To highlight the significance of these interactions in promoting tumor progression and identifying therapeutic targets.
Main Methods:
- Literature review focusing on the interplay between tumor cells, TAMs, microbiota, and TDEVs.
- Analysis of mechanisms by which TDEVs transfer malignant factors.
- Examination of how TDEVs influence TAMs and microbial communities in the TME.
Main Results:
- TDEVs act as crucial messengers, transferring factors that regulate TAM and microbial behavior.
- Tumor cells utilize TDEVs to recruit and influence both TAMs and microbes.
- Hijacked TAMs and microbes engage in feedback loops that promote tumor growth and survival within the TME.
Conclusions:
- TDEVs play a central role in orchestrating the complex interactions within the TME.
- Clarifying the specific crosstalk mediated by TDEVs is essential for identifying novel therapeutic strategies.
- Targeting TDEV-mediated communication pathways offers potential for improving cancer treatment and patient prognosis.
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