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Tissue and serum microRNA profile of oral squamous cell carcinoma patients
Head and neck cancer is characterized by malignant tumors arising from the epithelium covering the upper aerodigestive tract, and the majority of these epithelial malignancies are squamous cell carcinomas (SCCs) of the oral cavity (OSCCs). The aim of the current work was to identify miRNAs regulated...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766573/ https://www.ncbi.nlm.nih.gov/pubmed/29330429 http://dx.doi.org/10.1038/s41598-017-18945-z |
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author | Schneider, Augusto Victoria, Berta Lopez, Yury Nunez Suchorska, Wiktoria Barczak, Wojciech Sobecka, Agnieszka Golusinski, Wojciech Masternak, Michal M. Golusinski, Pawel |
author_facet | Schneider, Augusto Victoria, Berta Lopez, Yury Nunez Suchorska, Wiktoria Barczak, Wojciech Sobecka, Agnieszka Golusinski, Wojciech Masternak, Michal M. Golusinski, Pawel |
author_sort | Schneider, Augusto |
collection | PubMed |
description | Head and neck cancer is characterized by malignant tumors arising from the epithelium covering the upper aerodigestive tract, and the majority of these epithelial malignancies are squamous cell carcinomas (SCCs) of the oral cavity (OSCCs). The aim of the current work was to identify miRNAs regulated in OSCC cancerous tissue when compared to a healthy adjacent tissue and to verify the presence of the same miRNAs in the circulation of these patients. For that serum samples and biopsies of healthy and tumor tissues were collected from five patients diagnosed with OSCC of the oral cavity, RNA was extracted from these samples and microRNAs libraries were prepared and sequenced. A total 255 miRNAs were identified in tissue and 381 different miRNAs were identified in serum samples. When comparing the miRNA expression between tumor and healthy tissue we identified 48 miRNAs (25 down- and 23 up-regulated) that were differentially expressed (FDR < 0.05). From these 48 differentially expressed miRNAs in tissue, 30 miRNAs were also found in the serum of the same patients. hsa-miR-32-5p was up-regulated in tumor compared to healthy tissue in our study, and was previously shown to be up-regulated in the serum of OSCC patients. Therefore, this suggests that miRNAs can be used as potential non-invasive biomarkers of OSCC. |
format | Online Article Text |
id | pubmed-5766573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57665732018-01-17 Tissue and serum microRNA profile of oral squamous cell carcinoma patients Schneider, Augusto Victoria, Berta Lopez, Yury Nunez Suchorska, Wiktoria Barczak, Wojciech Sobecka, Agnieszka Golusinski, Wojciech Masternak, Michal M. Golusinski, Pawel Sci Rep Article Head and neck cancer is characterized by malignant tumors arising from the epithelium covering the upper aerodigestive tract, and the majority of these epithelial malignancies are squamous cell carcinomas (SCCs) of the oral cavity (OSCCs). The aim of the current work was to identify miRNAs regulated in OSCC cancerous tissue when compared to a healthy adjacent tissue and to verify the presence of the same miRNAs in the circulation of these patients. For that serum samples and biopsies of healthy and tumor tissues were collected from five patients diagnosed with OSCC of the oral cavity, RNA was extracted from these samples and microRNAs libraries were prepared and sequenced. A total 255 miRNAs were identified in tissue and 381 different miRNAs were identified in serum samples. When comparing the miRNA expression between tumor and healthy tissue we identified 48 miRNAs (25 down- and 23 up-regulated) that were differentially expressed (FDR < 0.05). From these 48 differentially expressed miRNAs in tissue, 30 miRNAs were also found in the serum of the same patients. hsa-miR-32-5p was up-regulated in tumor compared to healthy tissue in our study, and was previously shown to be up-regulated in the serum of OSCC patients. Therefore, this suggests that miRNAs can be used as potential non-invasive biomarkers of OSCC. Nature Publishing Group UK 2018-01-12 /pmc/articles/PMC5766573/ /pubmed/29330429 http://dx.doi.org/10.1038/s41598-017-18945-z Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Schneider, Augusto Victoria, Berta Lopez, Yury Nunez Suchorska, Wiktoria Barczak, Wojciech Sobecka, Agnieszka Golusinski, Wojciech Masternak, Michal M. Golusinski, Pawel Tissue and serum microRNA profile of oral squamous cell carcinoma patients |
title | Tissue and serum microRNA profile of oral squamous cell carcinoma patients |
title_full | Tissue and serum microRNA profile of oral squamous cell carcinoma patients |
title_fullStr | Tissue and serum microRNA profile of oral squamous cell carcinoma patients |
title_full_unstemmed | Tissue and serum microRNA profile of oral squamous cell carcinoma patients |
title_short | Tissue and serum microRNA profile of oral squamous cell carcinoma patients |
title_sort | tissue and serum microrna profile of oral squamous cell carcinoma patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5766573/ https://www.ncbi.nlm.nih.gov/pubmed/29330429 http://dx.doi.org/10.1038/s41598-017-18945-z |
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