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MicroRNA regulation in colorectal cancer tissue and serum

Colorectal cancer is recognized as the fourth leading cause of cancer-related deaths worldwide. Thus, there is ongoing search for potential new biomarkers allowing quicker and less invasive detection of the disease and prediction of the treatment outcome. Therefore, the aim of our study was to ident...

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Autores principales: Gmerek, Lukasz, Martyniak, Kari, Horbacka, Karolina, Krokowicz, Piotr, Scierski, Wojciech, Golusinski, Pawel, Golusinski, Wojciech, Schneider, Augusto, Masternak, Michal M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716664/
https://www.ncbi.nlm.nih.gov/pubmed/31469874
http://dx.doi.org/10.1371/journal.pone.0222013
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author Gmerek, Lukasz
Martyniak, Kari
Horbacka, Karolina
Krokowicz, Piotr
Scierski, Wojciech
Golusinski, Pawel
Golusinski, Wojciech
Schneider, Augusto
Masternak, Michal M.
author_facet Gmerek, Lukasz
Martyniak, Kari
Horbacka, Karolina
Krokowicz, Piotr
Scierski, Wojciech
Golusinski, Pawel
Golusinski, Wojciech
Schneider, Augusto
Masternak, Michal M.
author_sort Gmerek, Lukasz
collection PubMed
description Colorectal cancer is recognized as the fourth leading cause of cancer-related deaths worldwide. Thus, there is ongoing search for potential new biomarkers allowing quicker and less invasive detection of the disease and prediction of the treatment outcome. Therefore, the aim of our study was to identify colorectal cancer specific miRNAs expressed in cancerous and healthy tissue from the same patient and to further correlate the presence of the same miRNAs in the circulation as potential biomarkers for diagnosis. In the current study we detected a set of 40 miRNAs differentially regulated in tumor tissue when comparing with healthy tissue. Additionally, we found 8 miRNAs differentially regulated in serum of colorectal cancer patients. Interestingly, there was no overlap in miRNAs regulated in tissue and serum, suggesting that serum regulated miRNAs may be not actively secreted from colorectal tumor cells. However, four of differentially expressed miRNAs, including miR-21, miR-17, miR-20a and miR-32 represent the miRNAs characteristic for different tumor types, including breast, colon, lung, pancreas, prostate and stomach cancer. This finding suggests important groups of miRNAs which can be further validated as markers for diagnosis of tumor tissue and regulation of carcinogenesis.
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spelling pubmed-67166642019-09-16 MicroRNA regulation in colorectal cancer tissue and serum Gmerek, Lukasz Martyniak, Kari Horbacka, Karolina Krokowicz, Piotr Scierski, Wojciech Golusinski, Pawel Golusinski, Wojciech Schneider, Augusto Masternak, Michal M. PLoS One Research Article Colorectal cancer is recognized as the fourth leading cause of cancer-related deaths worldwide. Thus, there is ongoing search for potential new biomarkers allowing quicker and less invasive detection of the disease and prediction of the treatment outcome. Therefore, the aim of our study was to identify colorectal cancer specific miRNAs expressed in cancerous and healthy tissue from the same patient and to further correlate the presence of the same miRNAs in the circulation as potential biomarkers for diagnosis. In the current study we detected a set of 40 miRNAs differentially regulated in tumor tissue when comparing with healthy tissue. Additionally, we found 8 miRNAs differentially regulated in serum of colorectal cancer patients. Interestingly, there was no overlap in miRNAs regulated in tissue and serum, suggesting that serum regulated miRNAs may be not actively secreted from colorectal tumor cells. However, four of differentially expressed miRNAs, including miR-21, miR-17, miR-20a and miR-32 represent the miRNAs characteristic for different tumor types, including breast, colon, lung, pancreas, prostate and stomach cancer. This finding suggests important groups of miRNAs which can be further validated as markers for diagnosis of tumor tissue and regulation of carcinogenesis. Public Library of Science 2019-08-30 /pmc/articles/PMC6716664/ /pubmed/31469874 http://dx.doi.org/10.1371/journal.pone.0222013 Text en © 2019 Gmerek et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gmerek, Lukasz
Martyniak, Kari
Horbacka, Karolina
Krokowicz, Piotr
Scierski, Wojciech
Golusinski, Pawel
Golusinski, Wojciech
Schneider, Augusto
Masternak, Michal M.
MicroRNA regulation in colorectal cancer tissue and serum
title MicroRNA regulation in colorectal cancer tissue and serum
title_full MicroRNA regulation in colorectal cancer tissue and serum
title_fullStr MicroRNA regulation in colorectal cancer tissue and serum
title_full_unstemmed MicroRNA regulation in colorectal cancer tissue and serum
title_short MicroRNA regulation in colorectal cancer tissue and serum
title_sort microrna regulation in colorectal cancer tissue and serum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6716664/
https://www.ncbi.nlm.nih.gov/pubmed/31469874
http://dx.doi.org/10.1371/journal.pone.0222013
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