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Evaluation of miR-506 and miR-4316 expression in early and non-invasive diagnosis of colorectal cancer

PURPOSE: Examination of the entire colon by colonoscopy remains the golden standard for screening of colorectal cancer (CRC). However, patients are reluctant to perform invasive colonoscopies because of interference with their intimacy. Therefore, the potential use of non-invasive analysis of microR...

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Autores principales: Krawczyk, Paweł, Powrózek, Tomasz, Olesiński, Tomasz, Dmitruk, Adam, Dziwota, Joanna, Kowalski, Dariusz, Milanowski, Janusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486640/
https://www.ncbi.nlm.nih.gov/pubmed/28405738
http://dx.doi.org/10.1007/s00384-017-2814-8
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author Krawczyk, Paweł
Powrózek, Tomasz
Olesiński, Tomasz
Dmitruk, Adam
Dziwota, Joanna
Kowalski, Dariusz
Milanowski, Janusz
author_facet Krawczyk, Paweł
Powrózek, Tomasz
Olesiński, Tomasz
Dmitruk, Adam
Dziwota, Joanna
Kowalski, Dariusz
Milanowski, Janusz
author_sort Krawczyk, Paweł
collection PubMed
description PURPOSE: Examination of the entire colon by colonoscopy remains the golden standard for screening of colorectal cancer (CRC). However, patients are reluctant to perform invasive colonoscopies because of interference with their intimacy. Therefore, the potential use of non-invasive analysis of microRNAs expression in liquid biopsy as a novel biomarker for early CRC has investigated in several studies. In this study, we analyzed the expression of two novel microRNAs: miR-506 and miR-4316, which have never been examined in CRC. METHODS: Plasma samples were collected from 56 patients (median age of 68 years) with operable colorectal cancer and from 70 healthy individuals (median age of 59 years). Expression of plasma microRNAs was evaluated by quantitative reverse transcription polymerase chain reaction using Eco real-time PCR device (Illumina, USA). RESULTS: We found a significant elevated expression of both examined microRNAs in early CRC patients when compared to those in healthy individuals (p = 0.0054 for miR-506 and p = 0.0025 for miR-4316). The expression of miR-506 and miR-4316 did not depend on gender, age, disease stage, and tumor localization of CRC patients. ROC curve analysis showed that both examined microRNAs could differentiate early stage colorectal cancer from healthy individuals with 76.8% specificity and 60.7% sensitivity for miR-506 analysis and 76.8% specificity and 75% specificity for miR-4316 analysis. CONCLUSION: Our study revealed that elevated expression of miR-506 and miR-4316 in peripheral blood were potential molecular markers for early colorectal cancer.
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spelling pubmed-54866402017-07-11 Evaluation of miR-506 and miR-4316 expression in early and non-invasive diagnosis of colorectal cancer Krawczyk, Paweł Powrózek, Tomasz Olesiński, Tomasz Dmitruk, Adam Dziwota, Joanna Kowalski, Dariusz Milanowski, Janusz Int J Colorectal Dis Short Communication PURPOSE: Examination of the entire colon by colonoscopy remains the golden standard for screening of colorectal cancer (CRC). However, patients are reluctant to perform invasive colonoscopies because of interference with their intimacy. Therefore, the potential use of non-invasive analysis of microRNAs expression in liquid biopsy as a novel biomarker for early CRC has investigated in several studies. In this study, we analyzed the expression of two novel microRNAs: miR-506 and miR-4316, which have never been examined in CRC. METHODS: Plasma samples were collected from 56 patients (median age of 68 years) with operable colorectal cancer and from 70 healthy individuals (median age of 59 years). Expression of plasma microRNAs was evaluated by quantitative reverse transcription polymerase chain reaction using Eco real-time PCR device (Illumina, USA). RESULTS: We found a significant elevated expression of both examined microRNAs in early CRC patients when compared to those in healthy individuals (p = 0.0054 for miR-506 and p = 0.0025 for miR-4316). The expression of miR-506 and miR-4316 did not depend on gender, age, disease stage, and tumor localization of CRC patients. ROC curve analysis showed that both examined microRNAs could differentiate early stage colorectal cancer from healthy individuals with 76.8% specificity and 60.7% sensitivity for miR-506 analysis and 76.8% specificity and 75% specificity for miR-4316 analysis. CONCLUSION: Our study revealed that elevated expression of miR-506 and miR-4316 in peripheral blood were potential molecular markers for early colorectal cancer. Springer Berlin Heidelberg 2017-04-12 2017 /pmc/articles/PMC5486640/ /pubmed/28405738 http://dx.doi.org/10.1007/s00384-017-2814-8 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Short Communication
Krawczyk, Paweł
Powrózek, Tomasz
Olesiński, Tomasz
Dmitruk, Adam
Dziwota, Joanna
Kowalski, Dariusz
Milanowski, Janusz
Evaluation of miR-506 and miR-4316 expression in early and non-invasive diagnosis of colorectal cancer
title Evaluation of miR-506 and miR-4316 expression in early and non-invasive diagnosis of colorectal cancer
title_full Evaluation of miR-506 and miR-4316 expression in early and non-invasive diagnosis of colorectal cancer
title_fullStr Evaluation of miR-506 and miR-4316 expression in early and non-invasive diagnosis of colorectal cancer
title_full_unstemmed Evaluation of miR-506 and miR-4316 expression in early and non-invasive diagnosis of colorectal cancer
title_short Evaluation of miR-506 and miR-4316 expression in early and non-invasive diagnosis of colorectal cancer
title_sort evaluation of mir-506 and mir-4316 expression in early and non-invasive diagnosis of colorectal cancer
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486640/
https://www.ncbi.nlm.nih.gov/pubmed/28405738
http://dx.doi.org/10.1007/s00384-017-2814-8
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