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Decreased expression of miR-23b is associated with poor survival of endometrial cancer patients

Endometrial cancer (EC) is one of the most common types of cancer of the female reproductive system. EC is classified into two types (EC1 and EC2). MiRNAs are single-stranded RNA molecules that regulate gene expression posttranscriptionally. They have aberrant expression profiles in cancer, includin...

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Autores principales: Klicka, Klaudia, Grzywa, Tomasz M., Klinke, Alicja, Mielniczuk, Aleksandra, Wejman, Jarosław, Ostrowska, Joanna, Gondek, Agata, Włodarski, Paweł K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637218/
https://www.ncbi.nlm.nih.gov/pubmed/36335210
http://dx.doi.org/10.1038/s41598-022-22306-w
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author Klicka, Klaudia
Grzywa, Tomasz M.
Klinke, Alicja
Mielniczuk, Aleksandra
Wejman, Jarosław
Ostrowska, Joanna
Gondek, Agata
Włodarski, Paweł K.
author_facet Klicka, Klaudia
Grzywa, Tomasz M.
Klinke, Alicja
Mielniczuk, Aleksandra
Wejman, Jarosław
Ostrowska, Joanna
Gondek, Agata
Włodarski, Paweł K.
author_sort Klicka, Klaudia
collection PubMed
description Endometrial cancer (EC) is one of the most common types of cancer of the female reproductive system. EC is classified into two types (EC1 and EC2). MiRNAs are single-stranded RNA molecules that regulate gene expression posttranscriptionally. They have aberrant expression profiles in cancer, including EC. This study aimed to assess the level of expression of a panel of 16 miRNAs in both types of EC and healthy endometrium (HE). A total of 45 patients were enrolled into the study, 18 patients diagnosed with EC1, 12 diagnosed with EC2, and 15 HE controls. Tumor tissues or healthy endometrial tissues were dissected from archival formalin-fixed paraffin-embedded (FFPE) using laser capture microdissection (LCM). RNA was isolated from collected material and the expression of selected miRNAs was determined using the real-time qPCR. We found that miR-23b, miR-125b-5p, miR-199a-3p, miR-221-3p, and miR-451a were downregulated in EC in comparison to HE. Moreover, the expression of miR-34a-5p and miR-146-5p was higher in EC1 compared to EC2. Analysis of The Cancer Genome Atlas (TCGA) database confirmed decreased levels of miR-23b, miR-125b-5p, and miR-199a-3p in EC. Decreased miR-23b expression was associated with worse survival of EC patients.
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spelling pubmed-96372182022-11-07 Decreased expression of miR-23b is associated with poor survival of endometrial cancer patients Klicka, Klaudia Grzywa, Tomasz M. Klinke, Alicja Mielniczuk, Aleksandra Wejman, Jarosław Ostrowska, Joanna Gondek, Agata Włodarski, Paweł K. Sci Rep Article Endometrial cancer (EC) is one of the most common types of cancer of the female reproductive system. EC is classified into two types (EC1 and EC2). MiRNAs are single-stranded RNA molecules that regulate gene expression posttranscriptionally. They have aberrant expression profiles in cancer, including EC. This study aimed to assess the level of expression of a panel of 16 miRNAs in both types of EC and healthy endometrium (HE). A total of 45 patients were enrolled into the study, 18 patients diagnosed with EC1, 12 diagnosed with EC2, and 15 HE controls. Tumor tissues or healthy endometrial tissues were dissected from archival formalin-fixed paraffin-embedded (FFPE) using laser capture microdissection (LCM). RNA was isolated from collected material and the expression of selected miRNAs was determined using the real-time qPCR. We found that miR-23b, miR-125b-5p, miR-199a-3p, miR-221-3p, and miR-451a were downregulated in EC in comparison to HE. Moreover, the expression of miR-34a-5p and miR-146-5p was higher in EC1 compared to EC2. Analysis of The Cancer Genome Atlas (TCGA) database confirmed decreased levels of miR-23b, miR-125b-5p, and miR-199a-3p in EC. Decreased miR-23b expression was associated with worse survival of EC patients. Nature Publishing Group UK 2022-11-05 /pmc/articles/PMC9637218/ /pubmed/36335210 http://dx.doi.org/10.1038/s41598-022-22306-w Text en © The Author(s) 2022 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/) .
spellingShingle Article
Klicka, Klaudia
Grzywa, Tomasz M.
Klinke, Alicja
Mielniczuk, Aleksandra
Wejman, Jarosław
Ostrowska, Joanna
Gondek, Agata
Włodarski, Paweł K.
Decreased expression of miR-23b is associated with poor survival of endometrial cancer patients
title Decreased expression of miR-23b is associated with poor survival of endometrial cancer patients
title_full Decreased expression of miR-23b is associated with poor survival of endometrial cancer patients
title_fullStr Decreased expression of miR-23b is associated with poor survival of endometrial cancer patients
title_full_unstemmed Decreased expression of miR-23b is associated with poor survival of endometrial cancer patients
title_short Decreased expression of miR-23b is associated with poor survival of endometrial cancer patients
title_sort decreased expression of mir-23b is associated with poor survival of endometrial cancer patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637218/
https://www.ncbi.nlm.nih.gov/pubmed/36335210
http://dx.doi.org/10.1038/s41598-022-22306-w
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