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Clinical value of microRNA-19a-3p and microRNA-99a-5p in bladder cancer
INTRODUCTION: MicroRNAs (miRNA) are small (approximately 17 to 25 nucleotides in length), single stranded, non-coding RNAs that play an important role in the control of gene expression at the post-transcriptional stage, by inhibiting protein translation or promoting mRNA degradation. The main aim of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259381/ https://www.ncbi.nlm.nih.gov/pubmed/37313204 http://dx.doi.org/10.5114/aoms.2019.89700 |
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author | Borkowska, Edyta M. Kutwin, Piotr Rolecka, Dorota Konecki, Tomasz Borowiec, Maciej Jabłonowski, Zbigniew |
author_facet | Borkowska, Edyta M. Kutwin, Piotr Rolecka, Dorota Konecki, Tomasz Borowiec, Maciej Jabłonowski, Zbigniew |
author_sort | Borkowska, Edyta M. |
collection | PubMed |
description | INTRODUCTION: MicroRNAs (miRNA) are small (approximately 17 to 25 nucleotides in length), single stranded, non-coding RNAs that play an important role in the control of gene expression at the post-transcriptional stage, by inhibiting protein translation or promoting mRNA degradation. The main aim of the study was to evaluate the clinical utility of the tested markers (miRNAs 19a-3p and 99a-5p), which might be important in the diagnostics of non-invasive bladder cancer (BC). MATERIAL AND METHODS: The study involved a group of 60 patients suffering from BC (histopathologically confirmed), in which 20 patients were diagnosed with muscle invasive BC (INBC) and 40 patients with non-muscle invasive BC (NINBC). The control group consisted of 20 samples of normal urothelium, which did not show any cancerous changes during histopathological examination. We assessed the expression of microRNA, using real-time PCR and the miRCURY LNA Universal RT microRNA PCR Kit by Exiqon, Denmark. RESULTS: Reduced expression of both analyzed markers was observed in most cases: miR-19a-3p in 51.8% and miR-99a-5p in 65.5% (as follows Mann-Whitney U test p < 0.000001 and Student’s t test p = 0.034262). Moreover, miR-19a-3p in our tested group was useful to differentiate between low and high grade disease in non-invasive stages (t test p = 0.0315435). Furthermore, miR-19a-3p and miR-99a-5p were able to discriminate patients in low grade for groups with or without recurrence. CONCLUSIONS: Our data indicated that miR-19a-3p and miR-99a-5p were significantly altered in bladder cancer samples and useful as diagnostic markers. |
format | Online Article Text |
id | pubmed-10259381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-102593812023-06-13 Clinical value of microRNA-19a-3p and microRNA-99a-5p in bladder cancer Borkowska, Edyta M. Kutwin, Piotr Rolecka, Dorota Konecki, Tomasz Borowiec, Maciej Jabłonowski, Zbigniew Arch Med Sci Clinical Research INTRODUCTION: MicroRNAs (miRNA) are small (approximately 17 to 25 nucleotides in length), single stranded, non-coding RNAs that play an important role in the control of gene expression at the post-transcriptional stage, by inhibiting protein translation or promoting mRNA degradation. The main aim of the study was to evaluate the clinical utility of the tested markers (miRNAs 19a-3p and 99a-5p), which might be important in the diagnostics of non-invasive bladder cancer (BC). MATERIAL AND METHODS: The study involved a group of 60 patients suffering from BC (histopathologically confirmed), in which 20 patients were diagnosed with muscle invasive BC (INBC) and 40 patients with non-muscle invasive BC (NINBC). The control group consisted of 20 samples of normal urothelium, which did not show any cancerous changes during histopathological examination. We assessed the expression of microRNA, using real-time PCR and the miRCURY LNA Universal RT microRNA PCR Kit by Exiqon, Denmark. RESULTS: Reduced expression of both analyzed markers was observed in most cases: miR-19a-3p in 51.8% and miR-99a-5p in 65.5% (as follows Mann-Whitney U test p < 0.000001 and Student’s t test p = 0.034262). Moreover, miR-19a-3p in our tested group was useful to differentiate between low and high grade disease in non-invasive stages (t test p = 0.0315435). Furthermore, miR-19a-3p and miR-99a-5p were able to discriminate patients in low grade for groups with or without recurrence. CONCLUSIONS: Our data indicated that miR-19a-3p and miR-99a-5p were significantly altered in bladder cancer samples and useful as diagnostic markers. Termedia Publishing House 2020-10-13 /pmc/articles/PMC10259381/ /pubmed/37313204 http://dx.doi.org/10.5114/aoms.2019.89700 Text en Copyright: © 2020 Termedia & Banach https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Clinical Research Borkowska, Edyta M. Kutwin, Piotr Rolecka, Dorota Konecki, Tomasz Borowiec, Maciej Jabłonowski, Zbigniew Clinical value of microRNA-19a-3p and microRNA-99a-5p in bladder cancer |
title | Clinical value of microRNA-19a-3p and microRNA-99a-5p in bladder cancer |
title_full | Clinical value of microRNA-19a-3p and microRNA-99a-5p in bladder cancer |
title_fullStr | Clinical value of microRNA-19a-3p and microRNA-99a-5p in bladder cancer |
title_full_unstemmed | Clinical value of microRNA-19a-3p and microRNA-99a-5p in bladder cancer |
title_short | Clinical value of microRNA-19a-3p and microRNA-99a-5p in bladder cancer |
title_sort | clinical value of microrna-19a-3p and microrna-99a-5p in bladder cancer |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10259381/ https://www.ncbi.nlm.nih.gov/pubmed/37313204 http://dx.doi.org/10.5114/aoms.2019.89700 |
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