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Lectins as potential tools for cancer biomarker discovery from extracellular vesicles

Extracellular vesicles (EVs) have considerable potential as diagnostic, prognostic, and therapeutic agents, in large part because molecular patterns on the EV surface betray the cell of origin and may also be used to “target” EVs to specific cells. Cancer is associated with alterations to cellular a...

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Autores principales: Islam, Md. Khirul, Khan, Misba, Gidwani, Kamlesh, Witwer, Kenneth W., Lamminmäki, Urpo, Leivo, Janne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10540341/
https://www.ncbi.nlm.nih.gov/pubmed/37773167
http://dx.doi.org/10.1186/s40364-023-00520-6
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author Islam, Md. Khirul
Khan, Misba
Gidwani, Kamlesh
Witwer, Kenneth W.
Lamminmäki, Urpo
Leivo, Janne
author_facet Islam, Md. Khirul
Khan, Misba
Gidwani, Kamlesh
Witwer, Kenneth W.
Lamminmäki, Urpo
Leivo, Janne
author_sort Islam, Md. Khirul
collection PubMed
description Extracellular vesicles (EVs) have considerable potential as diagnostic, prognostic, and therapeutic agents, in large part because molecular patterns on the EV surface betray the cell of origin and may also be used to “target” EVs to specific cells. Cancer is associated with alterations to cellular and EV glycosylation patterns, and the surface of EVs is enriched with glycan moieties. Glycoconjugates of EVs play versatile roles in cancer including modulating immune response, affecting tumor cell behavior and site of metastasis and as such, paving the way for the development of innovative diagnostic tools and novel therapies. Entities that recognize specific glycans, such as lectins, may thus be powerful tools to discover and detect novel cancer biomarkers. Indeed, the past decade has seen a constant increase in the number of published articles on lectin-based strategies for the detection of EV glycans. This review explores the roles of EV glycosylation in cancer and cancer-related applications. Furthermore, this review summarizes the potential of lectins and lectin-based methods for screening, targeting, separation, and possible identification of improved biomarkers from the surface of EVs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-023-00520-6.
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spelling pubmed-105403412023-09-30 Lectins as potential tools for cancer biomarker discovery from extracellular vesicles Islam, Md. Khirul Khan, Misba Gidwani, Kamlesh Witwer, Kenneth W. Lamminmäki, Urpo Leivo, Janne Biomark Res Review Extracellular vesicles (EVs) have considerable potential as diagnostic, prognostic, and therapeutic agents, in large part because molecular patterns on the EV surface betray the cell of origin and may also be used to “target” EVs to specific cells. Cancer is associated with alterations to cellular and EV glycosylation patterns, and the surface of EVs is enriched with glycan moieties. Glycoconjugates of EVs play versatile roles in cancer including modulating immune response, affecting tumor cell behavior and site of metastasis and as such, paving the way for the development of innovative diagnostic tools and novel therapies. Entities that recognize specific glycans, such as lectins, may thus be powerful tools to discover and detect novel cancer biomarkers. Indeed, the past decade has seen a constant increase in the number of published articles on lectin-based strategies for the detection of EV glycans. This review explores the roles of EV glycosylation in cancer and cancer-related applications. Furthermore, this review summarizes the potential of lectins and lectin-based methods for screening, targeting, separation, and possible identification of improved biomarkers from the surface of EVs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-023-00520-6. BioMed Central 2023-09-29 /pmc/articles/PMC10540341/ /pubmed/37773167 http://dx.doi.org/10.1186/s40364-023-00520-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Islam, Md. Khirul
Khan, Misba
Gidwani, Kamlesh
Witwer, Kenneth W.
Lamminmäki, Urpo
Leivo, Janne
Lectins as potential tools for cancer biomarker discovery from extracellular vesicles
title Lectins as potential tools for cancer biomarker discovery from extracellular vesicles
title_full Lectins as potential tools for cancer biomarker discovery from extracellular vesicles
title_fullStr Lectins as potential tools for cancer biomarker discovery from extracellular vesicles
title_full_unstemmed Lectins as potential tools for cancer biomarker discovery from extracellular vesicles
title_short Lectins as potential tools for cancer biomarker discovery from extracellular vesicles
title_sort lectins as potential tools for cancer biomarker discovery from extracellular vesicles
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10540341/
https://www.ncbi.nlm.nih.gov/pubmed/37773167
http://dx.doi.org/10.1186/s40364-023-00520-6
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