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Development of a deregulating microRNA panel for the detection of early relapse in postoperative colorectal cancer patients
BACKGROUND: Colorectal cancer (CRC) is the third leading cause of cancer mortality worldwide and is associated with high recurrence and mortality, despite recent advancements in therapeutic strategies. MicroRNA (miR) deregulation is associated with CRC development and recurrence; therefore, miRs may...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850676/ https://www.ncbi.nlm.nih.gov/pubmed/27126129 http://dx.doi.org/10.1186/s12967-016-0856-2 |
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author | Yang, I-Ping Tsai, Hsiang-Lin Miao, Zhi-Feng Huang, Ching-Wen Kuo, Chao-Hung Wu, Jeng-Yih Wang, Wen-Ming Juo, Suh-Hang Hank Wang, Jaw-Yuan |
author_facet | Yang, I-Ping Tsai, Hsiang-Lin Miao, Zhi-Feng Huang, Ching-Wen Kuo, Chao-Hung Wu, Jeng-Yih Wang, Wen-Ming Juo, Suh-Hang Hank Wang, Jaw-Yuan |
author_sort | Yang, I-Ping |
collection | PubMed |
description | BACKGROUND: Colorectal cancer (CRC) is the third leading cause of cancer mortality worldwide and is associated with high recurrence and mortality, despite recent advancements in therapeutic strategies. MicroRNA (miR) deregulation is associated with CRC development and recurrence; therefore, miRs may be reliable biomarkers for detecting early relapse postoperatively. METHODS: In this study ten candidates were identified using miR arrays: miR-7, miR-31, miR-93, miR-141, miR-195, miR-375, miR-429, miR-494, miR-650, and let-7b. Substantial differences were observed in their expression levels between early relapsed (recurrences within 12 months after surgery) and non-early relapsed CRC patients. The validation study, including 50 early relapsed and 54 non-early relapsed patients, confirmed miR expression alterations in cancer tissue samples. RESULTS: Using a miR real-time quantitative polymerase chain reaction (RT-qPCR), we observed that expression levels of miR-93, miR-195, and let-7b were significantly decreased, whereas those of miR-7, miR-141 and miR-494 showed increases that were more significant in the CRC tissue samples from the early relapsed patients than in those from the non-early relapsed patients. Disease-free survival and overall survival were significantly worse in the high miR-7, miR-141, and miR-494 expression subgroups and the low miR-93 and miR-195 expression subgroups (all P < 0.05). A panel of 6 miRs (miR-7, miR-93, miR-195, miR-141, miR-494, and let-7b), at a cut-off value of 2 deregulated miRs, distinguished early relapsed CRC from non-early relapsed CRC, with a sensitivity of 76.6 % and a specificity of 71.4 %. By combining this 6-miRs panel with 6 clinicopathologic factors, at a cut-off value of 4, distinguished early relapsed CRC from non-early relapsed CRC, with a sensitivity of 89.4 % and a specificity of 88.9 %. CONCLUSIONS: This study showed that the developed miR panel has the potential to improve predicting early relapse in CRC patients. |
format | Online Article Text |
id | pubmed-4850676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48506762016-04-30 Development of a deregulating microRNA panel for the detection of early relapse in postoperative colorectal cancer patients Yang, I-Ping Tsai, Hsiang-Lin Miao, Zhi-Feng Huang, Ching-Wen Kuo, Chao-Hung Wu, Jeng-Yih Wang, Wen-Ming Juo, Suh-Hang Hank Wang, Jaw-Yuan J Transl Med Research BACKGROUND: Colorectal cancer (CRC) is the third leading cause of cancer mortality worldwide and is associated with high recurrence and mortality, despite recent advancements in therapeutic strategies. MicroRNA (miR) deregulation is associated with CRC development and recurrence; therefore, miRs may be reliable biomarkers for detecting early relapse postoperatively. METHODS: In this study ten candidates were identified using miR arrays: miR-7, miR-31, miR-93, miR-141, miR-195, miR-375, miR-429, miR-494, miR-650, and let-7b. Substantial differences were observed in their expression levels between early relapsed (recurrences within 12 months after surgery) and non-early relapsed CRC patients. The validation study, including 50 early relapsed and 54 non-early relapsed patients, confirmed miR expression alterations in cancer tissue samples. RESULTS: Using a miR real-time quantitative polymerase chain reaction (RT-qPCR), we observed that expression levels of miR-93, miR-195, and let-7b were significantly decreased, whereas those of miR-7, miR-141 and miR-494 showed increases that were more significant in the CRC tissue samples from the early relapsed patients than in those from the non-early relapsed patients. Disease-free survival and overall survival were significantly worse in the high miR-7, miR-141, and miR-494 expression subgroups and the low miR-93 and miR-195 expression subgroups (all P < 0.05). A panel of 6 miRs (miR-7, miR-93, miR-195, miR-141, miR-494, and let-7b), at a cut-off value of 2 deregulated miRs, distinguished early relapsed CRC from non-early relapsed CRC, with a sensitivity of 76.6 % and a specificity of 71.4 %. By combining this 6-miRs panel with 6 clinicopathologic factors, at a cut-off value of 4, distinguished early relapsed CRC from non-early relapsed CRC, with a sensitivity of 89.4 % and a specificity of 88.9 %. CONCLUSIONS: This study showed that the developed miR panel has the potential to improve predicting early relapse in CRC patients. BioMed Central 2016-04-29 /pmc/articles/PMC4850676/ /pubmed/27126129 http://dx.doi.org/10.1186/s12967-016-0856-2 Text en © Yang et al. 2016 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Yang, I-Ping Tsai, Hsiang-Lin Miao, Zhi-Feng Huang, Ching-Wen Kuo, Chao-Hung Wu, Jeng-Yih Wang, Wen-Ming Juo, Suh-Hang Hank Wang, Jaw-Yuan Development of a deregulating microRNA panel for the detection of early relapse in postoperative colorectal cancer patients |
title | Development of a deregulating microRNA panel for the detection of early relapse in postoperative colorectal cancer patients |
title_full | Development of a deregulating microRNA panel for the detection of early relapse in postoperative colorectal cancer patients |
title_fullStr | Development of a deregulating microRNA panel for the detection of early relapse in postoperative colorectal cancer patients |
title_full_unstemmed | Development of a deregulating microRNA panel for the detection of early relapse in postoperative colorectal cancer patients |
title_short | Development of a deregulating microRNA panel for the detection of early relapse in postoperative colorectal cancer patients |
title_sort | development of a deregulating microrna panel for the detection of early relapse in postoperative colorectal cancer patients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850676/ https://www.ncbi.nlm.nih.gov/pubmed/27126129 http://dx.doi.org/10.1186/s12967-016-0856-2 |
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