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Expression level of CD117 (KIT) on ovarian cancer extracellular vesicles correlates with tumor aggressiveness

Ovarian cancer is known to be the most lethal malignancy among all gynecological cancers affecting a large number of women worldwide. The treatment of ovarian cancer is challenging due to the high recurrence rate of the disease and is further complicated by acquired chemoresistance. Most ovarian can...

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Autores principales: Shnaider, Polina V., Petrushanko, Irina Yu., Aleshikova, Olga I., Babaeva, Nataliya A., Ashrafyan, Lev A., Borovkova, Ekaterina I., Dobrokhotova, Julia E., Borovkov, Ivan M., Shender, Victoria O., Khomyakova, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978408/
https://www.ncbi.nlm.nih.gov/pubmed/36875773
http://dx.doi.org/10.3389/fcell.2023.1057484
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author Shnaider, Polina V.
Petrushanko, Irina Yu.
Aleshikova, Olga I.
Babaeva, Nataliya A.
Ashrafyan, Lev A.
Borovkova, Ekaterina I.
Dobrokhotova, Julia E.
Borovkov, Ivan M.
Shender, Victoria O.
Khomyakova, Elena
author_facet Shnaider, Polina V.
Petrushanko, Irina Yu.
Aleshikova, Olga I.
Babaeva, Nataliya A.
Ashrafyan, Lev A.
Borovkova, Ekaterina I.
Dobrokhotova, Julia E.
Borovkov, Ivan M.
Shender, Victoria O.
Khomyakova, Elena
author_sort Shnaider, Polina V.
collection PubMed
description Ovarian cancer is known to be the most lethal malignancy among all gynecological cancers affecting a large number of women worldwide. The treatment of ovarian cancer is challenging due to the high recurrence rate of the disease and is further complicated by acquired chemoresistance. Most ovarian cancer deaths are the result of the metastatic spread of drug-resistant cells. The theory of cancer stem cells (CSC) suggests that both tumor initiation and progression are driven by a population of undifferentiated capable of self-renewal, tumor initiation and development of chemoresistance. The CD117 mast/stem cell growth factor receptor (KIT) is the most commonly used marker for ovarian CSCs. Here, we analyze the correlation between CD117 expression and histological tumor type in ovarian cancer cell lines (SK-OV-3 and MES-OV) and in small/medium extracellular vesicles (EVs) isolated from the urine of ovarian cancer patients. We have demonstrated that the abundance of CD117 on cells and EVs is correlated with tumor grade and therapy resistance status. Moreover, using small EVs isolated from ovarian cancer ascites, it was shown that recurrent disease is characterized by a much higher abundance of CD117 on EVs than primary tumor.
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spelling pubmed-99784082023-03-03 Expression level of CD117 (KIT) on ovarian cancer extracellular vesicles correlates with tumor aggressiveness Shnaider, Polina V. Petrushanko, Irina Yu. Aleshikova, Olga I. Babaeva, Nataliya A. Ashrafyan, Lev A. Borovkova, Ekaterina I. Dobrokhotova, Julia E. Borovkov, Ivan M. Shender, Victoria O. Khomyakova, Elena Front Cell Dev Biol Cell and Developmental Biology Ovarian cancer is known to be the most lethal malignancy among all gynecological cancers affecting a large number of women worldwide. The treatment of ovarian cancer is challenging due to the high recurrence rate of the disease and is further complicated by acquired chemoresistance. Most ovarian cancer deaths are the result of the metastatic spread of drug-resistant cells. The theory of cancer stem cells (CSC) suggests that both tumor initiation and progression are driven by a population of undifferentiated capable of self-renewal, tumor initiation and development of chemoresistance. The CD117 mast/stem cell growth factor receptor (KIT) is the most commonly used marker for ovarian CSCs. Here, we analyze the correlation between CD117 expression and histological tumor type in ovarian cancer cell lines (SK-OV-3 and MES-OV) and in small/medium extracellular vesicles (EVs) isolated from the urine of ovarian cancer patients. We have demonstrated that the abundance of CD117 on cells and EVs is correlated with tumor grade and therapy resistance status. Moreover, using small EVs isolated from ovarian cancer ascites, it was shown that recurrent disease is characterized by a much higher abundance of CD117 on EVs than primary tumor. Frontiers Media S.A. 2023-02-16 /pmc/articles/PMC9978408/ /pubmed/36875773 http://dx.doi.org/10.3389/fcell.2023.1057484 Text en Copyright © 2023 Shnaider, Petrushanko, Aleshikova, Babaeva, Ashrafyan, Borovkova, Dobrokhotova, Borovkov, Shender and Khomyakova. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Shnaider, Polina V.
Petrushanko, Irina Yu.
Aleshikova, Olga I.
Babaeva, Nataliya A.
Ashrafyan, Lev A.
Borovkova, Ekaterina I.
Dobrokhotova, Julia E.
Borovkov, Ivan M.
Shender, Victoria O.
Khomyakova, Elena
Expression level of CD117 (KIT) on ovarian cancer extracellular vesicles correlates with tumor aggressiveness
title Expression level of CD117 (KIT) on ovarian cancer extracellular vesicles correlates with tumor aggressiveness
title_full Expression level of CD117 (KIT) on ovarian cancer extracellular vesicles correlates with tumor aggressiveness
title_fullStr Expression level of CD117 (KIT) on ovarian cancer extracellular vesicles correlates with tumor aggressiveness
title_full_unstemmed Expression level of CD117 (KIT) on ovarian cancer extracellular vesicles correlates with tumor aggressiveness
title_short Expression level of CD117 (KIT) on ovarian cancer extracellular vesicles correlates with tumor aggressiveness
title_sort expression level of cd117 (kit) on ovarian cancer extracellular vesicles correlates with tumor aggressiveness
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978408/
https://www.ncbi.nlm.nih.gov/pubmed/36875773
http://dx.doi.org/10.3389/fcell.2023.1057484
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