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Glycosylation of Cancer Extracellular Vesicles: Capture Strategies, Functional Roles and Potential Clinical Applications

期刊

CELLS
卷 10, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/cells10010109

关键词

extracellular vesicles; glycosylation; cancer; biomarker; therapy; detection; capture; exosomes

资金

  1. FEDER funds through the Operational Programme for Competitiveness Factors COMPETE [POCI-01-0145-FEDER-016585, POCI-01-0145-FEDER-007274]
  2. Foundation for Science and Technology (FCT) [PTDC/BBB-EBI/0567/2014, UID/BIM/04293/2013, NORTE-01-0145FEDER-000029]
  3. Norte Portugal Regional Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF)

向作者/读者索取更多资源

Glycans and glycoproteins are commonly used in clinical settings as cancer biomarkers, and alterations in glycosylation pathways in cancer cells give rise to specific glycans. EV glycosylation has potential applications in distinguishing tumor EVs from benign EVs and developing novel detection methods.
Glycans are major constituents of extracellular vesicles (EVs). Alterations in the glycosylation pathway are a common feature of cancer cells, which gives rise to de novo or increased synthesis of particular glycans. Therefore, glycans and glycoproteins have been widely used in the clinic as both stratification and prognosis cancer biomarkers. Interestingly, several of the known tumor-associated glycans have already been identified in cancer EVs, highlighting EV glycosylation as a potential source of circulating cancer biomarkers. These particles are crucial vehicles of cell-cell communication, being able to transfer molecular information and to modulate the recipient cell behavior. The presence of particular glycoconjugates has been described to be important for EV protein sorting, uptake and organ-tropism. Furthermore, specific EV glycans or glycoproteins have been described to be able to distinguish tumor EVs from benign EVs. In this review, the application of EV glycosylation in the development of novel EV detection and capture methodologies is discussed. In addition, we highlight the potential of EV glycosylation in the clinical setting for both cancer biomarker discovery and EV therapeutic delivery strategies.

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