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  1. Strutture

Exosome-Mediated Therapeutic Strategies for Management of Solid and Hematological Malignancies

Articolo
Data di Pubblicazione:
2022
Abstract:
Exosomes are small membrane vesicles of endocytic origin containing cytokines, RNAs, growth factors, proteins, lipids, and metabolites. They have been identified as fundamental intercellular communication controllers in several diseases and an enormous volume of data confirmed that exosomes could either sustain or inhibit tumor onset and diffusion in diverse solid and hematological malignancies by paracrine signaling. Thus, exosomes might constitute a promising cell-free tumor treatment alternative. This review focuses on the effects of exosomes in the treatment of tumors, by discussing the most recent and promising data from in vitro and experimental in vivo studies and the few existing clinical trials. Exosomes are extremely promising as transporters of drugs, antagomir, genes, and other therapeutic substances that can be integrated into their core via different procedures. Moreover, exosomes can augment or inhibit non-coding RNAs, change the metabolism of cancer cells, and modify the function of immunologic effectors thus modifying the tumor microenvironment transforming it from pro-tumor to antitumor milieu. Here, we report the development of currently realized exosome modifiers that offer indications for the forthcoming elaboration of other more effective methods capable of enhancing the activity of the exosomes.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Cell Communication; Exosomes; Hematologic Neoplasms; Humans; Neoplasms; Tumor Microenvironment
Elenco autori:
Allegra, Alessandro; Petrarca, Claudia; DI GIOACCHINO, Mario; Casciaro, Marco; Musolino, Caterina; Gangemi, Sebastiano
Autori di Ateneo:
PETRARCA CLAUDIA
Link alla scheda completa:
https://ricerca.unich.it/handle/11564/772991
Link al Full Text:
https://ricerca.unich.it//retrieve/handle/11564/772991/313991/cells-11-01128-v2.pdf
Pubblicato in:
CELLS
Journal
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URL

https://www.mdpi.com/2073-4409/11/7/1128
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