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Article: From Exosome Biogenesis to Absorption: Key Takeaways for Cancer Research

TitleFrom Exosome Biogenesis to Absorption: Key Takeaways for Cancer Research
Authors
Keywordsbiogenesis
cancer
endocytosis
exosome
extracellular vesicle
intercellular communication
regulation
targeting
Issue Date27-Mar-2023
PublisherMDPI
Citation
Cancers, 2023, v. 15, n. 7 How to Cite?
Abstract

Exosomes are mediators of intercellular communication in normal physiology and diseases. While many studies have emerged on the function of exosomal cargoes, questions remain regarding the origin of these exosomes. The packaging and secretion of exosomes in different contexts modify exosomal composition, which may in turn impact delivery, uptake and cargo function in recipient cells. A mechanistic understanding of exosome biology is therefore crucial to investigating exosomal function in complex biological systems and to the development of novel therapeutic approaches. Here, we outline the steps in exosome biogenesis, including endosome formation, MVB formation, cargo sorting and extracellular release, as well as exosome absorption, including targeting, interaction with recipient cells and the fate of internalized exosomes. In addition to providing a framework of exosome dynamics, we summarize current evidence on major pathways and regulatory mechanisms. We also highlight the various mechanisms observed in cancer and point out directions to improve study design in exosome biology. Further research is needed to illuminate the relationship between exosome biogenesis and function, which will aid the development of translational applications.


Persistent Identifierhttp://hdl.handle.net/10722/331270
ISSN
2023 Impact Factor: 4.5
2023 SCImago Journal Rankings: 1.391
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLau, NCH-
dc.contributor.authorYam, JWP-
dc.date.accessioned2023-09-21T06:54:13Z-
dc.date.available2023-09-21T06:54:13Z-
dc.date.issued2023-03-27-
dc.identifier.citationCancers, 2023, v. 15, n. 7-
dc.identifier.issn2072-6694-
dc.identifier.urihttp://hdl.handle.net/10722/331270-
dc.description.abstract<p>Exosomes are mediators of intercellular communication in normal physiology and diseases. While many studies have emerged on the function of exosomal cargoes, questions remain regarding the origin of these exosomes. The packaging and secretion of exosomes in different contexts modify exosomal composition, which may in turn impact delivery, uptake and cargo function in recipient cells. A mechanistic understanding of exosome biology is therefore crucial to investigating exosomal function in complex biological systems and to the development of novel therapeutic approaches. Here, we outline the steps in exosome biogenesis, including endosome formation, MVB formation, cargo sorting and extracellular release, as well as exosome absorption, including targeting, interaction with recipient cells and the fate of internalized exosomes. In addition to providing a framework of exosome dynamics, we summarize current evidence on major pathways and regulatory mechanisms. We also highlight the various mechanisms observed in cancer and point out directions to improve study design in exosome biology. Further research is needed to illuminate the relationship between exosome biogenesis and function, which will aid the development of translational applications.</p>-
dc.languageeng-
dc.publisherMDPI-
dc.relation.ispartofCancers-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectbiogenesis-
dc.subjectcancer-
dc.subjectendocytosis-
dc.subjectexosome-
dc.subjectextracellular vesicle-
dc.subjectintercellular communication-
dc.subjectregulation-
dc.subjecttargeting-
dc.titleFrom Exosome Biogenesis to Absorption: Key Takeaways for Cancer Research-
dc.typeArticle-
dc.identifier.doi10.3390/cancers15071992-
dc.identifier.pmid37046653-
dc.identifier.scopuseid_2-s2.0-85152575497-
dc.identifier.volume15-
dc.identifier.issue7-
dc.identifier.eissn2072-6694-
dc.identifier.isiWOS:000969591400001-
dc.identifier.issnl2072-6694-

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