Tumor hijacks macrophages and microbiota through extracellular vesicles

Jipeng Jiang(Chinese PLA General Hospital), Jie Mei(National Center for Nanoscience and Technology), Yongfu Ma(Chinese PLA General Hospital), Shasha Jiang(Chinese PLA General Hospital), Jian Zhang(Chinese PLA General Hospital), Shaoqiong Yi(Chinese PLA General Hospital), Changjiang Feng(Chinese PLA General Hospital), Yang Liu(Chinese PLA General Hospital), Ying Liu(Chinese PLA General Hospital)
Exploration
January 25, 2022
Cited by 82Open Access
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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.


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