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Microparticles in cancer
1Montreal Children's Hospital Research Institute, McGill University, Montreal, Quebec, Canada. janusz.rak@mcgill.ca
Abstract:
Microparticles (MP) are vesicular structures released from cells upon activation, malignant transformation, stress, or death. MP may be derived from the plasma membrane (shed microvesicles), produced by endosomal pathway (exosomes), or arise from membrane blebs of apoptotic cells. The terms microparticles or microvesicles (MV) are often used as general and interchangeable descriptors of all cellular vesicles, but a more rigorous terminology is still to be established. The cargo of MP/MV consists of proteins, lipids, and nucleic acids (DNA, mRNA, microRNA), all of which may be transferred horizontally between cells. In cancer, oncogenic pathways drive production of MP/MV, and oncoproteins may be incorporated into the cargo of MV (oncosomes). Oncogenic pathways may also stimulate production of MP/MV harboring tissue factor and involved in cancer coagulopathy. In addition, the cargo of MV may include several receptors, antigens, bioactive molecules, and other species capable of stimulating tumor progression, immunotolerance, invasion, angiogenesis, and metastasis. MP emanate not only from tumor cells but also from platelets, endothelium, and inflammatory cells. Indeed, circulating MP/MV harbor molecular information related to cancer-related processes and may serve as a reservoir of prognostic and predictive biomarkers to monitor genetic tumor progression, angiogenesis, thrombosis, and responses to targeted therapeutics.
Insights
Cellular microparticles (MP) carry cancer-related molecules and can be used as biomarkers. These vesicles, released from various cells, provide insights into tumor progression and treatment response.
Area of Science:
- Cell Biology
- Oncology
- Biochemistry
Background:
- Microparticles (MP) are cell-derived vesicles released during cellular activation, stress, or death.
- These vesicles, including exosomes and shed microvesicles, contain proteins, lipids, and nucleic acids.
- Current terminology for these vesicles is not standardized, with 'microparticles' and 'microvesicles' (MV) often used interchangeably.
Purpose of the Study:
- To review the role of microparticles in cancer.
- To highlight the molecular cargo of microparticles and their impact on tumor progression.
- To discuss the potential of microparticles as prognostic and predictive biomarkers in oncology.
Main Methods:
- Literature review of studies on microparticles in cancer.
- Analysis of the composition and function of microparticle cargo.
- Evaluation of microparticles as biomarkers for cancer monitoring.
Main Results:
- Oncogenic pathways increase microparticle production, incorporating oncoproteins and tissue factor.
- Microparticle cargo can promote tumor progression, invasion, angiogenesis, and metastasis.
- Circulating microparticles reflect cancer-specific molecular information.
Conclusions:
- Microparticles are key mediators in cancer progression and metastasis.
- Microparticles serve as valuable reservoirs for biomarkers to monitor tumor genetic evolution, angiogenesis, and treatment efficacy.
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