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Endothelin-3 is epigenetically silenced in endometrioid endometrial cancer

PURPOSE: Changes in the activity of endothelins and their receptors may promote neoplastic processes. They can be caused by epigenetic modifications and modulators, but little is known about endothelin-3 (EDN3), particularly in endometrial cancer. The aim of the study was to determine the expression...

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Autores principales: Zmarzły, Nikola, Januszyk, Szymon, Mieszczański, Paweł, Morawiec, Emilia, Buda, Paulina, Dziobek, Konrad, Opławski, Marcin, Boroń, Dariusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356642/
https://www.ncbi.nlm.nih.gov/pubmed/36542159
http://dx.doi.org/10.1007/s00432-022-04525-w
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author Zmarzły, Nikola
Januszyk, Szymon
Mieszczański, Paweł
Morawiec, Emilia
Buda, Paulina
Dziobek, Konrad
Opławski, Marcin
Boroń, Dariusz
author_facet Zmarzły, Nikola
Januszyk, Szymon
Mieszczański, Paweł
Morawiec, Emilia
Buda, Paulina
Dziobek, Konrad
Opławski, Marcin
Boroń, Dariusz
author_sort Zmarzły, Nikola
collection PubMed
description PURPOSE: Changes in the activity of endothelins and their receptors may promote neoplastic processes. They can be caused by epigenetic modifications and modulators, but little is known about endothelin-3 (EDN3), particularly in endometrial cancer. The aim of the study was to determine the expression profile of endothelin family and their interactions with miRNAs, and to assess the degree of EDN3 methylation. METHODS: The study enrolled 45 patients with endometrioid endometrial cancer and 30 patients without neoplastic changes. The expression profile of endothelins and their receptors was determined with mRNA microarrays and RT-qPCR. The miRNA prediction was based on the miRNA microarray experiment and the mirDB tool. The degree of EDN3 methylation was assessed by MSP. RESULTS: EDN1 and EDNRA were overexpressed regardless of endometrial cancer grade, which may be due to the lack of regulatory effect of miR-130a-3p and miR-485-3p, respectively. In addition, EDN3 and EDNRB were significantly downregulated. CONCLUSION: The endothelial axis is disturbed in endometrioid endometrial cancer. The observed silencing of EDN3 activity may be mainly due to DNA methylation.
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spelling pubmed-103566422023-07-21 Endothelin-3 is epigenetically silenced in endometrioid endometrial cancer Zmarzły, Nikola Januszyk, Szymon Mieszczański, Paweł Morawiec, Emilia Buda, Paulina Dziobek, Konrad Opławski, Marcin Boroń, Dariusz J Cancer Res Clin Oncol Research PURPOSE: Changes in the activity of endothelins and their receptors may promote neoplastic processes. They can be caused by epigenetic modifications and modulators, but little is known about endothelin-3 (EDN3), particularly in endometrial cancer. The aim of the study was to determine the expression profile of endothelin family and their interactions with miRNAs, and to assess the degree of EDN3 methylation. METHODS: The study enrolled 45 patients with endometrioid endometrial cancer and 30 patients without neoplastic changes. The expression profile of endothelins and their receptors was determined with mRNA microarrays and RT-qPCR. The miRNA prediction was based on the miRNA microarray experiment and the mirDB tool. The degree of EDN3 methylation was assessed by MSP. RESULTS: EDN1 and EDNRA were overexpressed regardless of endometrial cancer grade, which may be due to the lack of regulatory effect of miR-130a-3p and miR-485-3p, respectively. In addition, EDN3 and EDNRB were significantly downregulated. CONCLUSION: The endothelial axis is disturbed in endometrioid endometrial cancer. The observed silencing of EDN3 activity may be mainly due to DNA methylation. Springer Berlin Heidelberg 2022-12-21 2023 /pmc/articles/PMC10356642/ /pubmed/36542159 http://dx.doi.org/10.1007/s00432-022-04525-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) .
spellingShingle Research
Zmarzły, Nikola
Januszyk, Szymon
Mieszczański, Paweł
Morawiec, Emilia
Buda, Paulina
Dziobek, Konrad
Opławski, Marcin
Boroń, Dariusz
Endothelin-3 is epigenetically silenced in endometrioid endometrial cancer
title Endothelin-3 is epigenetically silenced in endometrioid endometrial cancer
title_full Endothelin-3 is epigenetically silenced in endometrioid endometrial cancer
title_fullStr Endothelin-3 is epigenetically silenced in endometrioid endometrial cancer
title_full_unstemmed Endothelin-3 is epigenetically silenced in endometrioid endometrial cancer
title_short Endothelin-3 is epigenetically silenced in endometrioid endometrial cancer
title_sort endothelin-3 is epigenetically silenced in endometrioid endometrial cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10356642/
https://www.ncbi.nlm.nih.gov/pubmed/36542159
http://dx.doi.org/10.1007/s00432-022-04525-w
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