Brain Tumor-Derived Extracellular Vesicles as Carriers of Disease Markers: Molecular Chaperones and MicroRNAs

• Main Authors: Alessandra Maria Vitale, Radha Santonocito, Giuseppe Vergilio, Antonella Marino Gammazza, Claudia Campanella, Everly Conway de Macario, Fabio Bucchieri, Alberto J. L. Macario, Celeste Caruso Bavisotto
• Format: Article
• Language: English
• Published: MDPI AG 2020-10-01
• Series: Applied Sciences
• Subjects: brain tumors; extracellular vesicles; miRNA; molecular chaperones; diagnostic tools; drug delivery
• Online Access: https://www.mdpi.com/2076-3417/10/19/6961

Primary and metastatic brain tumors are usually serious conditions with poor prognosis, which reveal the urgent need of developing rapid diagnostic tools and efficacious treatments. To achieve these objectives, progress must be made in the understanding of brain tumor biology, for example, how they resist natural defenses and therapeutic intervention. One resistance mechanism involves extracellular vesicles that are released by tumors to meet target cells nearby or distant via circulation and reprogram them by introducing their cargo. This consists of different molecules among which are microRNAs (miRNAs) and molecular chaperones, the focus of this article. miRNAs modify target cells in the immune system to avoid antitumor reaction and chaperones are key survival molecules for the tumor cell. Extracellular vesicles cargo reflects the composition and metabolism of the original tumor cell; therefore, it is a source of markers, including the miRNAs and chaperones discussed in this article, with potential diagnostic and prognostic value. This and their relatively easy availability by minimally invasive procedures (e.g., drawing venous blood) illustrate the potential of extracellular vesicles as useful materials to manage brain tumor patients. Furthermore, understanding extracellular vesicles circulation and interaction with target cells will provide the basis for using this vesicle for delivering therapeutic compounds to selected tumor cells.