Related Experiment Video
Updated: Jul 6, 2025

LINE-1 Methylation Analysis in Mesenchymal Stem Cells Treated with Osteosarcoma-Derived Extracellular Vesicles
Published on: February 1, 2020
The multifaceted roles of small extracellular vesicles in metabolic reprogramming in the tumor microenvironments
Zhixian Chen1, Judy Wai Ping Yam1, Xiaowen Mao2
1Department of Pathology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Abstract:
The link between metabolism and tumor progression has been extensively researched for a long time. With the increasing number of studies uncovering the multiple functions of metabolic reprogramming in tumor microenvironments, the regulatory network seems to become even more intricate at the same time. Small extracellular vesicles (sEV), as crucial mediators facilitating intercellular communications, exhibit significant involvement in regulating metabolic reprogramming within the complicated network of tumor microenvironments. sEV derived from tumor cells and those released by other cell populations such as tumor-associated macrophages (TAMs) and cancer-associated fibroblasts (CAFs) can mutually influence each other, giving rise to diverse complex feedback loops. This review includes multiple studies conducted in recent years to summarize the functions of sEV in altering metabolism in various cell types within tumor microenvironments. Additionally, it aims to highlight potential therapeutic targets based on the commonly observed mechanisms identified in different studies.
Insights
Small extracellular vesicles (sEVs) are key players in tumor progression, mediating communication between cancer cells, macrophages, and fibroblasts. This review summarizes how sEVs alter metabolism in the tumor microenvironment and suggests therapeutic targets.
Area of Science:
- Oncology
- Cell Biology
- Metabolic Research
Background:
- The relationship between metabolism and tumor progression is complex and involves intricate regulatory networks within the tumor microenvironment.
- Metabolic reprogramming is increasingly recognized for its multifaceted roles in cancer development and progression.
- Intercellular communication is vital in shaping the tumor microenvironment, with small extracellular vesicles (sEVs) emerging as critical mediators.
Purpose of the Study:
- To review and summarize the diverse functions of sEVs in modulating cellular metabolism within the tumor microenvironment.
- To highlight the complex feedback loops established by sEVs derived from various cell types (tumor cells, TAMs, CAFs).
- To identify potential therapeutic targets based on the mechanisms of sEV-mediated metabolic reprogramming.
Main Methods:
- Comprehensive literature review of recent studies on sEVs and tumor metabolism.
- Analysis of research focusing on sEVs derived from tumor cells, tumor-associated macrophages (TAMs), and cancer-associated fibroblasts (CAFs).
- Synthesis of findings regarding the impact of sEVs on metabolic reprogramming in different cell types within the tumor microenvironment.
Main Results:
- sEVs play a significant role in facilitating intercellular communication and regulating metabolic reprogramming in tumor microenvironments.
- sEVs from tumor cells, TAMs, and CAFs engage in mutual interactions, creating complex feedback loops that influence tumor progression.
- Specific mechanisms by which sEVs alter metabolism in various cell types have been identified across multiple studies.
Conclusions:
- sEVs are crucial regulators of metabolic reprogramming within the tumor microenvironment, impacting cancer progression.
- Understanding the intricate roles of sEVs in intercellular communication offers new avenues for therapeutic intervention.
- Targeting sEV-mediated metabolic pathways presents a promising strategy for cancer treatment.
Related Concept Videos
The Tumor Microenvironment
Overview of Exosomes
Stahl et al. discovered exosomes in 1983, but the exosomes were initially considered waste products released from the...
Metastasis
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
Adaptive Mechanisms in Cancer Cells
Some of the advantages that cancer cells have on normal cells include - enhanced ability to divide without terminally differentiating, induce new blood vessel formation,...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Receptor Downregulation in MVBs
The EGFR can initiate signaling pathways that lead to cell proliferation, migration, and differentiation. Overexpression of EGFR stimulates cells to proliferate. Excessive EGFR...

