Migrasomes in the tumor microenvironment: Functional roles and therapeutic potential
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Updated: Jan 8, 2026

Characterization of the Effects of Migrastatic Inhibitors on 3D Tumor Spheroid Invasion by High-resolution Confocal Microscopy
Published on: September 16, 2019
Xinxin Li1, Jinshan Yang2, Hao Xie1
1School of Clinical Medicine, Shandong Second Medical University, Weifang, 261000, Shandong, China; Department of Urology, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.
Abstract:
Migrasomes are large extracellular vesicles (0.5-3 μm in diameter) with a distinctive pomegranate-like structure, formed along retraction fibers during cell migration and released their content through migracytosis. Unlike other extracellular vesicles, migrasomes play unique roles in intercellular communication by transferring proteins, RNAs, and signaling molecules within the tumor microenvironment. This review summarizes recent advances in understanding migrasome biogenesis, composition, and functional roles in cancer progression. We highlight their contributions to tumor angiogenesis, extracellular matrix remodeling, and most notably immune escape, through the regulation of tumor-associated macrophages, T cells, and other immune and stromal cells. Pan-cancer evidence supports a strong correlation between migrasome abundance and immunosuppressive gene signatures, including immune checkpoint expression and tumor immune dysfunction and exclusion (TIDE) scores. We also highlight the promising diagnostic and therapeutic potential of migrasomes as novel biomarkers and targets for cancer therapy. Finally, we discuss current research challenges and outline future directions for advancing migrasome research toward clinical translation.
Insights
Migrasomes, large vesicles involved in cell communication, significantly impact cancer progression. Their abundance correlates with immune suppression, highlighting their potential as diagnostic and therapeutic targets in oncology.
Area of Science:
- Cell Biology
- Cancer Research
- Immunology
Background:
- Migrasomes are large extracellular vesicles (0.5-3 µm) with a unique pomegranate structure, formed during cell migration.
- They facilitate intercellular communication by transferring proteins, RNAs, and signaling molecules, particularly within the tumor microenvironment.
- Unlike other extracellular vesicles, migrasomes have distinct roles in cancer progression.
Purpose of the Study:
- To review recent advances in understanding migrasome biogenesis, composition, and functional roles in cancer.
- To highlight migrasome contributions to tumor angiogenesis, ECM remodeling, and immune escape.
- To discuss the diagnostic and therapeutic potential of migrasomes in cancer therapy.
Main Methods:
- Literature review of recent scientific advances in migrasome research.
- Analysis of pan-cancer evidence correlating migrasome abundance with gene signatures.
- Examination of migrasome roles in regulating immune and stromal cells within the tumor microenvironment.
Main Results:
- Migrasomes contribute to tumor angiogenesis, extracellular matrix remodeling, and immune escape.
- They regulate tumor-associated macrophages, T cells, and other immune/stromal cells.
- High migrasome abundance correlates with immunosuppressive gene signatures, immune checkpoint expression, and TIDE scores.
Conclusions:
- Migrasomes play significant roles in cancer progression and immune evasion.
- They show promising potential as novel biomarkers and therapeutic targets for cancer.
- Further research is needed to advance migrasome understanding toward clinical translation.
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