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Updated: Jul 10, 2026

In Vivo Immunogenicity Screening of Tumor-Derived Extracellular Vesicles by Flow Cytometry of Splenic T Cells
Published on: September 23, 2021
Extracellular vesicles as systems-level regulators of tumor progression: Integrating signaling networks,
Deepthi Maria Mathew1, Ankit Kumar Bharti S1, Anirban Goutam Mukherjee2
1Department of Bio-Medical Sciences, School of Bio Sciences & Technology, Vellore Institute of Technology, Vellore, Tamil Nadu 632014, India.
Abstract:
Extracellular vesicles (EVs), once considered cellular debris, are now recognized as critical mediators of intercellular communication that regulate multiple aspects of tumor progression. Rather than acting through isolated pathways, EVs function as system-level regulators integrating intercellular signalling networks, cargo sorting mechanisms and tumor microenvironmental cues to coordinate dynamic and interconnected oncogenic responses. Unlike previous reviews that discuss these processes individually, this review adopts an integrative system-level framework linking EV-mediated oncogenic signaling, microenvironmental remodeling, angiogenesis, premetastatic niche formation, and therapy resistance that can lead to tumor progression. Accumulating evidence highlights EVs as systems-level regulators that integrate oncogenic signaling, microenvironmental remodeling, and adaptive tumor responses. This review presents a mechanistically focused overview of EV biology, moving beyond descriptive aspects of biogenesis to emphasize its functional roles in coordinating cancer progression. EVs facilitate the transfer of bioactive cargo, including proteins, nucleic acids, and lipids, thereby modulating key oncogenic signaling pathways such as PI3K/Akt, Wnt/β-catenin, and TGF-β, which collectively drive proliferation, invasion, and cellular plasticity. In addition, EVs play a pivotal role in reprogramming the tumor microenvironment by promoting angiogenesis, stromal activation, immune modulation, and pre-metastatic niche formation. Emerging evidence further implicates EVs in therapy resistance, where they contribute to drug efflux and the horizontal transfer of resistance-associated molecules. The functional heterogeneity of EV subpopulations and their context-dependent roles are also discussed as key determinants of disease progression. From a translational perspective, EVs are increasingly explored as minimally invasive biomarkers for cancer diagnosis and prognosis, as well as versatile platforms for targeted drug delivery. However, challenges related to isolation techniques, standardization, and clinical scalability remain significant barriers to their implementation. Collectively, this review provides a systems-level perspective on EV-mediated communication networks in cancer, underscoring their dual role as central drivers of tumor progression and promising targets for therapeutic intervention.
Insights
Extracellular vesicles (EVs) are key regulators of cancer progression, integrating signaling networks and the tumor microenvironment. This review highlights their roles in tumor growth, metastasis, and therapy resistance, offering insights for diagnostics and drug delivery.
Area of Science:
- Oncology and Cell Biology
- Cancer Research
- Intercellular Communication
Background:
- Extracellular vesicles (EVs) were once dismissed as cellular debris.
- They are now recognized as critical mediators of intercellular communication in cancer.
- EVs integrate complex signaling networks and tumor microenvironment cues to drive oncogenic responses.
Purpose of the Study:
- To provide a systems-level framework for understanding EV-mediated cancer progression.
- To link EV signaling, microenvironmental remodeling, angiogenesis, metastasis, and therapy resistance.
- To emphasize the functional roles of EVs in coordinating cancer progression.
Main Methods:
- Review of existing literature on EV biology and function in cancer.
- Mechanistically focused overview of EV biogenesis and cargo transfer.
- Analysis of EV roles in oncogenic signaling pathways (e.g., PI3K/Akt, Wnt/β-catenin, TGF-β).
Main Results:
- EVs transfer bioactive cargo, modulating key oncogenic pathways driving proliferation and invasion.
- EVs reprogram the tumor microenvironment, promoting angiogenesis, immune modulation, and pre-metastatic niche formation.
- EVs contribute to therapy resistance through drug efflux and horizontal transfer of resistance molecules.
Conclusions:
- EVs act as systems-level regulators, integrating diverse processes to drive tumor progression.
- EVs are implicated in cancer diagnosis, prognosis, and targeted drug delivery, despite technical challenges.
- Understanding EV networks is crucial for developing novel cancer therapies.
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