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Updated: Jun 2, 2026

Isolation and Characterization of Microvesicles from Peripheral Blood
Published on: January 6, 2017
The role of microvesicles in malignancies
1Department of Genetics, Cell- and Immunobiology, Semmelweis University, 1089, Budapest, Hungary. nyierna@dgci.sote.hu
Abstract:
Microvesicles are membrane-covered cell fragments whose size varies between 30 and 1,000 nm. They are generated by all cell types, constituvely and in response to activation signals. Their importance in intercellular communication has been only recently discovered. They seem to enhance the potential of information transfer between cells, displaying a large number of proteins and lipids as membrane constituents and as components of the inner vesicular content. The content reflects the phenotype of the donor cell and allows the identification of the microvesicular origine as well. Complex "packets" of molecules are transmitted to the target cells this way, modifying their cellular physiology. Additionally, epigenetic changes may be induced by transmitted DNA and RNAs, that have also been identified in these vesicles. The vesicles can act in close and far distances as well. Microvesicles have been implicated in several physiological and pathological processes. There is an increasing evidence, that they play a pivotal role in tumorigenesis. Vesicles shedding from tumor cells reflect the special potential of the tumor for survival and expansion, independently from cell-to-cell contact. Tumor derived vesicles are fully equipped to facilitate the escape of tumor cells from immune surveillance through their protein and RNA content, at the same time they are involved in the establishment of an optimal environment for newly formed and metastatic tumor cells, influencing angiogenesis and the reorganization of the extracellular matrix. As immune cells, endothels, platelets and stem cells also release microvesicles, a multilevel communication network draws up, allowing a complex interplay between the cells. The concentration of tumor derived vesicles increases in blood plasma and other body fluids with the progression of the disease; therefor they may serve as prognostic markers. The microvesicular approach can offer new perspectives: interfering with the formation, release and propagation of these vesicles, they can be considered as new targets in tumor therapy.
Insights
Microvesicles, small cell fragments, facilitate intercellular communication and are implicated in cancer. Targeting these vesicles offers new therapeutic strategies for tumors.
Area of Science:
- Cell Biology
- Molecular Biology
- Oncology
Background:
- Microvesicles are cell fragments (30-1,000 nm) involved in intercellular communication.
- They carry proteins, lipids, DNA, and RNA, reflecting donor cell phenotype.
- Their role in physiological and pathological processes, especially cancer, is increasingly recognized.
Purpose of the Study:
- To review the multifaceted roles of microvesicles in intercellular communication.
- To highlight the significance of microvesicles in tumorigenesis and cancer progression.
- To explore the potential of microvesicles as prognostic markers and therapeutic targets in cancer.
Main Methods:
- Literature review of microvesicle biogenesis, content, and function.
- Analysis of microvesicle involvement in intercellular signaling pathways.
- Examination of microvesicles in cancer, including immune evasion and metastasis.
Main Results:
- Microvesicles mediate intercellular communication by transferring molecular cargo.
- Tumor-derived microvesicles promote tumor survival, immune escape, and metastasis.
- Microvesicles influence angiogenesis and extracellular matrix remodeling.
- Elevated levels of tumor microvesicles in body fluids suggest prognostic value.
Conclusions:
- Microvesicles are crucial mediators of cell-to-cell communication with significant roles in cancer.
- Therapeutic strategies targeting microvesicle formation, release, or propagation show promise.
- Microvesicles represent potential biomarkers for cancer progression and novel therapeutic targets.
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