Articolo in rivista, 2022, ENG, 10.3390/biomedicines10081886
Cifola, Ingrid; Fratini, Federica; Cardinali, Beatrice; Palmieri, Valentina; Gatti, Giuliana; Selmi, Tommaso; Donzelli, Sara; Sacconi, Andrea; Cesarini, Valeriana; Marei, Hany E.; Papi, Massimilano; Blandino, Giovanni; Cenciarelli, Carlo; Falcone, Germana; D'Agnano, Igea
CNR; Ist Super Sanita ISS; CNR; Fdn Policlin Univ A Gemelli IRCSS; Univ Cattolica Sacro Cuore; CNR; Univ Milan; IRCCS Regina Elena Natl Canc Inst; IRCCS Regina Elena Natl Canc Inst; CNR; Mansoura Univ
Glioblastoma (GBM) is the most common and aggressive brain tumor in adults. Despite available therapeutic interventions, it is very difficult to treat, and a cure is not yet available. The intra-tumoral GBM heterogeneity is a crucial factor contributing to poor clinical outcomes. GBM derives from a small heterogeneous population of cancer stem cells (CSCs). In cancer tissue, CSCs are concentrated within the so-called niches, where they progress from a slowly proliferating phase. CSCs, as most tumor cells, release extracellular vesicles (EVs) into the surrounding microenvironment. To explore the role of EVs in CSCs and GBM tumor cells, we investigated the miRNA and protein content of the small EVs (sEVs) secreted by two GBM-established cell lines and by GBM primary CSCs using omics analysis. Our data indicate that GBM-sEVs are selectively enriched for miRNAs that are known to display tumor suppressor activity, while their protein cargo is enriched for oncoproteins and tumor-associated proteins. Conversely, among the most up-regulated miRNAs in CSC-sEVs, we also found pro-tumor miRNAs and proteins related to sternness, cell proliferation, and apoptosis. Collectively, our findings support the hypothesis that sEVs selectively incorporate different miRNAs and proteins belonging both to fundamental processes (e.g., cell proliferation, cell death, sternness) as well as to more specialized ones (e.g., EMT, membrane docking, cell junction organization, ncRNA processing).
Biomedicine (Amsterdam. Online) 10 (8)
glioblastoma, cancer stem cells, extracellular vesicles, miRNAs, proteome
ID: 486195
Year: 2022
Type: Articolo in rivista
Creation: 2023-09-11 14:38:22.000
Last update: 2023-09-11 15:57:46.000
CNR authors
External IDs
CNR OAI-PMH: oai:it.cnr:prodotti:486195
DOI: 10.3390/biomedicines10081886
ISI Web of Science (WOS): 000847178300001