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High expression of miR-17-5p and miR-20a-5p predicts favorable disease-specific survival in stage I-III colon cancer
In many types of cancer, microRNAs (miRs) are aberrantly expressed. The aim of this study was to explore the prognostic impact of miR-17-5p and miR-20a-5p in colon cancer. Tumor tissue from 452 stage I-III colon cancer patients was retrospectively collected and tissue microarrays constructed. miR-17...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056518/ https://www.ncbi.nlm.nih.gov/pubmed/35490164 http://dx.doi.org/10.1038/s41598-022-11090-2 |
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author | Selven, Hallgeir Andersen, Sigve Pedersen, Mona I. Lombardi, Ana Paola Giometti Busund, Lill-Tove Rasmussen Kilvær, Thomas Karsten |
author_facet | Selven, Hallgeir Andersen, Sigve Pedersen, Mona I. Lombardi, Ana Paola Giometti Busund, Lill-Tove Rasmussen Kilvær, Thomas Karsten |
author_sort | Selven, Hallgeir |
collection | PubMed |
description | In many types of cancer, microRNAs (miRs) are aberrantly expressed. The aim of this study was to explore the prognostic impact of miR-17-5p and miR-20a-5p in colon cancer. Tumor tissue from 452 stage I-III colon cancer patients was retrospectively collected and tissue microarrays constructed. miR-17-5p and miR-20a-5p expression was evaluated by in situ hybridization and analyzed using digital pathology. Cell line experiments, using HT-29 and CACO-2, were performed to assess the effect of miR-17-5p and miR-20a-5p over expression on viability, invasion and migration. In multivariate analyses, high miR-17-5p expression in tumor (HR = 0.43, CI 0.26–0.71, p < 0.001) and high expression of miR-20a-5p in tumor (HR = 0.60, CI 0.37–0.97, p = 0.037) and stroma (HR = 0.63, CI 0.42–0.95, p = 0.027) remained independent predictors of improved disease-specific survival. In cell lines, over expression of both miRs resulted in mitigated migration without any significant effect on viability or invasion. In conclusion, in stage I-III colon cancer, high expression of both miR-17-5p and miR-20a-5p are independent predictors of favorable prognosis. |
format | Online Article Text |
id | pubmed-9056518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90565182022-05-02 High expression of miR-17-5p and miR-20a-5p predicts favorable disease-specific survival in stage I-III colon cancer Selven, Hallgeir Andersen, Sigve Pedersen, Mona I. Lombardi, Ana Paola Giometti Busund, Lill-Tove Rasmussen Kilvær, Thomas Karsten Sci Rep Article In many types of cancer, microRNAs (miRs) are aberrantly expressed. The aim of this study was to explore the prognostic impact of miR-17-5p and miR-20a-5p in colon cancer. Tumor tissue from 452 stage I-III colon cancer patients was retrospectively collected and tissue microarrays constructed. miR-17-5p and miR-20a-5p expression was evaluated by in situ hybridization and analyzed using digital pathology. Cell line experiments, using HT-29 and CACO-2, were performed to assess the effect of miR-17-5p and miR-20a-5p over expression on viability, invasion and migration. In multivariate analyses, high miR-17-5p expression in tumor (HR = 0.43, CI 0.26–0.71, p < 0.001) and high expression of miR-20a-5p in tumor (HR = 0.60, CI 0.37–0.97, p = 0.037) and stroma (HR = 0.63, CI 0.42–0.95, p = 0.027) remained independent predictors of improved disease-specific survival. In cell lines, over expression of both miRs resulted in mitigated migration without any significant effect on viability or invasion. In conclusion, in stage I-III colon cancer, high expression of both miR-17-5p and miR-20a-5p are independent predictors of favorable prognosis. Nature Publishing Group UK 2022-04-30 /pmc/articles/PMC9056518/ /pubmed/35490164 http://dx.doi.org/10.1038/s41598-022-11090-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Selven, Hallgeir Andersen, Sigve Pedersen, Mona I. Lombardi, Ana Paola Giometti Busund, Lill-Tove Rasmussen Kilvær, Thomas Karsten High expression of miR-17-5p and miR-20a-5p predicts favorable disease-specific survival in stage I-III colon cancer |
title | High expression of miR-17-5p and miR-20a-5p predicts favorable disease-specific survival in stage I-III colon cancer |
title_full | High expression of miR-17-5p and miR-20a-5p predicts favorable disease-specific survival in stage I-III colon cancer |
title_fullStr | High expression of miR-17-5p and miR-20a-5p predicts favorable disease-specific survival in stage I-III colon cancer |
title_full_unstemmed | High expression of miR-17-5p and miR-20a-5p predicts favorable disease-specific survival in stage I-III colon cancer |
title_short | High expression of miR-17-5p and miR-20a-5p predicts favorable disease-specific survival in stage I-III colon cancer |
title_sort | high expression of mir-17-5p and mir-20a-5p predicts favorable disease-specific survival in stage i-iii colon cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056518/ https://www.ncbi.nlm.nih.gov/pubmed/35490164 http://dx.doi.org/10.1038/s41598-022-11090-2 |
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