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MiRNA profiling of gastrointestinal stromal tumors by next-generation sequencing
Deregulation of miRNAs has been observed virtually in all major types of cancer, whereas the miRNA signature in GIST is not well characterized yet. In this study the first high-throughput miRNA profiling of 15 paired GIST and adjacent normal tissue samples was performed using small RNA-seq approach...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514905/ https://www.ncbi.nlm.nih.gov/pubmed/28402935 http://dx.doi.org/10.18632/oncotarget.16664 |
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author | Gyvyte, Ugne Juzenas, Simonas Salteniene, Violeta Kupcinskas, Juozas Poskiene, Lina Kucinskas, Laimutis Jarmalaite, Sonata Stuopelyte, Kristina Steponaitiene, Ruta Hemmrich-Stanisak, Georg Hübenthal, Matthias Link, Alexander Franke, Sabine Franke, Andre Pangonyte, Dalia Lesauskaite, Vaiva Kupcinskas, Limas Skieceviciene, Jurgita |
author_facet | Gyvyte, Ugne Juzenas, Simonas Salteniene, Violeta Kupcinskas, Juozas Poskiene, Lina Kucinskas, Laimutis Jarmalaite, Sonata Stuopelyte, Kristina Steponaitiene, Ruta Hemmrich-Stanisak, Georg Hübenthal, Matthias Link, Alexander Franke, Sabine Franke, Andre Pangonyte, Dalia Lesauskaite, Vaiva Kupcinskas, Limas Skieceviciene, Jurgita |
author_sort | Gyvyte, Ugne |
collection | PubMed |
description | Deregulation of miRNAs has been observed virtually in all major types of cancer, whereas the miRNA signature in GIST is not well characterized yet. In this study the first high-throughput miRNA profiling of 15 paired GIST and adjacent normal tissue samples was performed using small RNA-seq approach and differentially expressed miRNAs as well as isomiRNAs were defined. Highly significantly deregulated miRNAs were selected for validation by Taq-Man low-density array in replication group of 40 paired samples. Validated miRNAs were further subjected to enrichment analysis, which revealed significantly enriched KEGG pathways in the main GIST associated pathways. Further, we used an integrated analysis of miRNA-mRNA correlations for KIT and PDGFRA target genes and found a significant correlation between all of the enriched miRNAs and their target gene KIT. Results of the phenotype analysis showed miR-509-3p to be up-regulated in epithelioid and mixed cell types compared to spindle type, whereas miR-215-5p showed negative correlation with risk grade of GIST. These data reveal a detailed miRNA profile of GIST and highlight new candidates that may be important in the development of malignant disease. |
format | Online Article Text |
id | pubmed-5514905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55149052017-07-24 MiRNA profiling of gastrointestinal stromal tumors by next-generation sequencing Gyvyte, Ugne Juzenas, Simonas Salteniene, Violeta Kupcinskas, Juozas Poskiene, Lina Kucinskas, Laimutis Jarmalaite, Sonata Stuopelyte, Kristina Steponaitiene, Ruta Hemmrich-Stanisak, Georg Hübenthal, Matthias Link, Alexander Franke, Sabine Franke, Andre Pangonyte, Dalia Lesauskaite, Vaiva Kupcinskas, Limas Skieceviciene, Jurgita Oncotarget Research Paper Deregulation of miRNAs has been observed virtually in all major types of cancer, whereas the miRNA signature in GIST is not well characterized yet. In this study the first high-throughput miRNA profiling of 15 paired GIST and adjacent normal tissue samples was performed using small RNA-seq approach and differentially expressed miRNAs as well as isomiRNAs were defined. Highly significantly deregulated miRNAs were selected for validation by Taq-Man low-density array in replication group of 40 paired samples. Validated miRNAs were further subjected to enrichment analysis, which revealed significantly enriched KEGG pathways in the main GIST associated pathways. Further, we used an integrated analysis of miRNA-mRNA correlations for KIT and PDGFRA target genes and found a significant correlation between all of the enriched miRNAs and their target gene KIT. Results of the phenotype analysis showed miR-509-3p to be up-regulated in epithelioid and mixed cell types compared to spindle type, whereas miR-215-5p showed negative correlation with risk grade of GIST. These data reveal a detailed miRNA profile of GIST and highlight new candidates that may be important in the development of malignant disease. Impact Journals LLC 2017-03-29 /pmc/articles/PMC5514905/ /pubmed/28402935 http://dx.doi.org/10.18632/oncotarget.16664 Text en Copyright: © 2017 Gyvyte et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Gyvyte, Ugne Juzenas, Simonas Salteniene, Violeta Kupcinskas, Juozas Poskiene, Lina Kucinskas, Laimutis Jarmalaite, Sonata Stuopelyte, Kristina Steponaitiene, Ruta Hemmrich-Stanisak, Georg Hübenthal, Matthias Link, Alexander Franke, Sabine Franke, Andre Pangonyte, Dalia Lesauskaite, Vaiva Kupcinskas, Limas Skieceviciene, Jurgita MiRNA profiling of gastrointestinal stromal tumors by next-generation sequencing |
title | MiRNA profiling of gastrointestinal stromal tumors by next-generation sequencing |
title_full | MiRNA profiling of gastrointestinal stromal tumors by next-generation sequencing |
title_fullStr | MiRNA profiling of gastrointestinal stromal tumors by next-generation sequencing |
title_full_unstemmed | MiRNA profiling of gastrointestinal stromal tumors by next-generation sequencing |
title_short | MiRNA profiling of gastrointestinal stromal tumors by next-generation sequencing |
title_sort | mirna profiling of gastrointestinal stromal tumors by next-generation sequencing |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514905/ https://www.ncbi.nlm.nih.gov/pubmed/28402935 http://dx.doi.org/10.18632/oncotarget.16664 |
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