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Extracellular Vesicles from Uterine Aspirates Represent a Promising Source for Screening Markers of Gynecologic Cancers

Extracellular vesicles (EVs), including exosomes, are key factors of intercellular communication, performing both local and distant transfers of bioactive molecules. The increasingly obvious role of EVs in carcinogenesis, similarity of molecular signatures with parental cells, precise selection and...

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Autores principales: Skryabin, Gleb O., Komelkov, Andrey V., Zhordania, Kirill I., Bagrov, Dmitry V., Vinokurova, Svetlana V., Galetsky, Sergey A., Elkina, Nadezhda V., Denisova, Darya A., Enikeev, Adel D., Tchevkina, Elena M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997481/
https://www.ncbi.nlm.nih.gov/pubmed/35406627
http://dx.doi.org/10.3390/cells11071064
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author Skryabin, Gleb O.
Komelkov, Andrey V.
Zhordania, Kirill I.
Bagrov, Dmitry V.
Vinokurova, Svetlana V.
Galetsky, Sergey A.
Elkina, Nadezhda V.
Denisova, Darya A.
Enikeev, Adel D.
Tchevkina, Elena M.
author_facet Skryabin, Gleb O.
Komelkov, Andrey V.
Zhordania, Kirill I.
Bagrov, Dmitry V.
Vinokurova, Svetlana V.
Galetsky, Sergey A.
Elkina, Nadezhda V.
Denisova, Darya A.
Enikeev, Adel D.
Tchevkina, Elena M.
author_sort Skryabin, Gleb O.
collection PubMed
description Extracellular vesicles (EVs), including exosomes, are key factors of intercellular communication, performing both local and distant transfers of bioactive molecules. The increasingly obvious role of EVs in carcinogenesis, similarity of molecular signatures with parental cells, precise selection and high stability of cargo molecules make exosomes a promising source of liquid biopsy markers for cancer diagnosis. The uterine cavity fluid, unlike blood, urine and other body fluids commonly used to study EVs, is of local origin and therefore enriched in EVs secreted by cells of the female reproductive tract. Here, we show that EVs, including those corresponding to exosomes, could be isolated from individual samples of uterine aspirates (UA) obtained from epithelial ovarian cancer (EOC) patients and healthy donors using the ultracentrifugation technique. First, the conducted profiling of small RNAs (small RNA-seq) from UA-derived EVs demonstrated the presence of non-coding RNA molecules belonging to various classes. The analysis of the miRNA content in EVs from UA performed on a pilot sample revealed significant differences in the expression levels of a number of miRNAs in EVs obtained from EOC patients compared to healthy individuals. The results open up prospects for using UA-derived EVs as a source of markers for the diagnostics of gynecological cancers, including EOC.
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spelling pubmed-89974812022-04-12 Extracellular Vesicles from Uterine Aspirates Represent a Promising Source for Screening Markers of Gynecologic Cancers Skryabin, Gleb O. Komelkov, Andrey V. Zhordania, Kirill I. Bagrov, Dmitry V. Vinokurova, Svetlana V. Galetsky, Sergey A. Elkina, Nadezhda V. Denisova, Darya A. Enikeev, Adel D. Tchevkina, Elena M. Cells Article Extracellular vesicles (EVs), including exosomes, are key factors of intercellular communication, performing both local and distant transfers of bioactive molecules. The increasingly obvious role of EVs in carcinogenesis, similarity of molecular signatures with parental cells, precise selection and high stability of cargo molecules make exosomes a promising source of liquid biopsy markers for cancer diagnosis. The uterine cavity fluid, unlike blood, urine and other body fluids commonly used to study EVs, is of local origin and therefore enriched in EVs secreted by cells of the female reproductive tract. Here, we show that EVs, including those corresponding to exosomes, could be isolated from individual samples of uterine aspirates (UA) obtained from epithelial ovarian cancer (EOC) patients and healthy donors using the ultracentrifugation technique. First, the conducted profiling of small RNAs (small RNA-seq) from UA-derived EVs demonstrated the presence of non-coding RNA molecules belonging to various classes. The analysis of the miRNA content in EVs from UA performed on a pilot sample revealed significant differences in the expression levels of a number of miRNAs in EVs obtained from EOC patients compared to healthy individuals. The results open up prospects for using UA-derived EVs as a source of markers for the diagnostics of gynecological cancers, including EOC. MDPI 2022-03-22 /pmc/articles/PMC8997481/ /pubmed/35406627 http://dx.doi.org/10.3390/cells11071064 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Skryabin, Gleb O.
Komelkov, Andrey V.
Zhordania, Kirill I.
Bagrov, Dmitry V.
Vinokurova, Svetlana V.
Galetsky, Sergey A.
Elkina, Nadezhda V.
Denisova, Darya A.
Enikeev, Adel D.
Tchevkina, Elena M.
Extracellular Vesicles from Uterine Aspirates Represent a Promising Source for Screening Markers of Gynecologic Cancers
title Extracellular Vesicles from Uterine Aspirates Represent a Promising Source for Screening Markers of Gynecologic Cancers
title_full Extracellular Vesicles from Uterine Aspirates Represent a Promising Source for Screening Markers of Gynecologic Cancers
title_fullStr Extracellular Vesicles from Uterine Aspirates Represent a Promising Source for Screening Markers of Gynecologic Cancers
title_full_unstemmed Extracellular Vesicles from Uterine Aspirates Represent a Promising Source for Screening Markers of Gynecologic Cancers
title_short Extracellular Vesicles from Uterine Aspirates Represent a Promising Source for Screening Markers of Gynecologic Cancers
title_sort extracellular vesicles from uterine aspirates represent a promising source for screening markers of gynecologic cancers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8997481/
https://www.ncbi.nlm.nih.gov/pubmed/35406627
http://dx.doi.org/10.3390/cells11071064
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