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Updated: May 21, 2026

Tracking miRNA Release into Extracellular Vesicles using Flow Cytometry
Published on: October 6, 2023
Microparticles in tumor progression
Anna Falanga1, Carmen Julia Tartari, Marina Marchetti
1Division of Immunohematology and Transfusion Medicine, Department of Oncology-Hematology, Ospedali Riuniti di Bergamo, Bergamo, Italy. annafalanga@yahoo.com
Abstract:
Microparticles (MP) are shed from the surface of activated or apoptotic blood cells and their levels in plasma reflect a balance between cell stimulation, proliferation, and death. MP production occurs through vesiculation of cell membranes, and involves cytoskeletal changes and a shift in the normal phospholipid asymmetry. The expression on the majority of MP of the anionic phosphatidylserine (PS) is responsible for the capacity of MP to support blood coagulation activation. In some cases, PS expression is also associated, in the same MP, with the presence of active Tissue Factor, the main activator of blood coagulation. Elevation in plasma levels of MP have been described in numerous clinical conditions, most of which also associated with an increased thrombotic risk. Particularly, MP have been found to be increased in both solid and hematological malignancies, including myeloproliferative neoplasms. A role of MP in tumor progression has been suggested by both in vitro and in vivo studies. Evidence exists that MP of platelet origin are the main players in this process, being rich in pro-angiogenic factors. The utility of measuring MP as a diagnostic and prognostic marker is currently a subject of intense investigation. The possibility to inhibit MP production by pharmacological interventions represents a future challenge.
Insights
Microparticles (MPs), released from blood cells, indicate cell death and disease. Elevated MPs, particularly from platelets, are linked to cancer and clotting risks, suggesting diagnostic potential.
Area of Science:
- Hematology
- Oncology
- Biochemistry
Background:
- Microparticles (MPs) are cell membrane fragments released during cell activation or apoptosis.
- Their plasma levels reflect cellular dynamics and can indicate disease states.
- Phosphatidylserine (PS) expression on MPs facilitates blood coagulation, especially when coupled with Tissue Factor.
Purpose of the Study:
- To review the role of MPs in various clinical conditions, particularly malignancies.
- To explore the association between elevated MPs and thrombotic risk.
- To discuss the potential of MPs as diagnostic and prognostic markers.
Main Methods:
- Literature review of studies investigating MP production and function.
- Analysis of MP levels in patients with different clinical conditions, including malignancies.
- Examination of the pro-angiogenic and pro-coagulant properties of MPs.
Main Results:
- Increased MP levels are observed in numerous clinical conditions, correlating with heightened thrombotic risk.
- Elevated MPs are particularly noted in solid and hematological malignancies, such as myeloproliferative neoplasms.
- Platelet-derived MPs are implicated in tumor progression due to their pro-angiogenic factor content.
Conclusions:
- MPs are significant biomarkers associated with increased thrombotic risk and cancer progression.
- Further research is needed to establish the utility of MPs as diagnostic and prognostic tools.
- Pharmacological inhibition of MP production presents a future therapeutic avenue.
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