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Updated: Nov 15, 2025

In Vivo Immunogenicity Screening of Tumor-Derived Extracellular Vesicles by Flow Cytometry of Splenic T Cells
Published on: September 23, 2021
Extracellular Vesicles: Emerging Modulators of Cancer Drug Resistance
Fabrizio Fontana1, Emanuela Carollo2, Genevieve E Melling2,3
1Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, via Balzaretti 9, 20133 Milan, Italy.
Abstract:
Extracellular vesicles (EVs) have recently emerged as crucial modulators of cancer drug resistance. Indeed, it has been shown that they can directly sequester anti-tumor drugs, decreasing their effective concentration at target sites. Moreover, they facilitate the horizontal transfer of specific bioactive cargoes able to regulate proliferative, apoptotic, and stemness programs in recipient cells, potentially conferring a resistant phenotype to drug-sensitive cancer cells. Finally, EVs can mediate the communication between the tumor and both stromal and immune cells within the microenvironment, promoting treatment escape. In this context, clarifying the EV-driven resistance mechanisms might improve not only tumor diagnosis and prognosis but also therapeutic outcomes. Detailed cellular and molecular events occurring during the development of EV-mediated cancer drug resistance are described in this review article.
Insights
Extracellular vesicles (EVs) are key to cancer drug resistance. These vesicles can sequester drugs and transfer molecules, promoting treatment failure and impacting tumor progression.
Area of Science:
- Oncology
- Cell Biology
- Biochemistry
Background:
- Extracellular vesicles (EVs) play a significant role in cancer progression.
- EVs are increasingly recognized as mediators of cancer drug resistance.
- Understanding EV-mediated resistance is crucial for improving cancer therapy.
Purpose of the Study:
- To review the cellular and molecular mechanisms of EV-mediated cancer drug resistance.
- To highlight the role of EVs in drug sequestration and horizontal gene transfer.
- To discuss the impact of EVs on tumor-stromal and tumor-immune cell communication.
Main Methods:
- Literature review of studies on EVs and cancer drug resistance.
- Analysis of mechanisms including drug sequestration, cargo transfer, and microenvironment modulation.
- Synthesis of current knowledge on EV-driven resistance pathways.
Main Results:
- EVs can directly sequester anti-cancer drugs, reducing their efficacy.
- EVs facilitate the transfer of bioactive molecules, inducing drug resistance in recipient cells.
- EVs mediate intercellular communication, promoting tumor survival and treatment escape.
Conclusions:
- EVs are critical players in the development of cancer drug resistance.
- Targeting EV-mediated mechanisms could offer novel therapeutic strategies.
- Further research into EV biology is essential for advancing cancer treatment and patient outcomes.
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