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Identification of a sixteen-microRNA signature as prognostic biomarker for stage II and III colon cancer

Despite advances in colon cancer research and novel therapies, high risk of recurrence remains a major challenge. This study reports miRNA expression profiling as a biomarker for the prognosis of TNM stage II and III colon cancer. Fresh frozen biopsies from the study cohort (N=111) were analyzed for...

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Autores principales: Jacob, Havjin, Stanisavljevic, Luka, Storli, Kristian Eeg, Hestetun, Kjersti E, Dahl, Olav, Myklebust, Mette P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5675676/
https://www.ncbi.nlm.nih.gov/pubmed/29152124
http://dx.doi.org/10.18632/oncotarget.21237
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author Jacob, Havjin
Stanisavljevic, Luka
Storli, Kristian Eeg
Hestetun, Kjersti E
Dahl, Olav
Myklebust, Mette P
author_facet Jacob, Havjin
Stanisavljevic, Luka
Storli, Kristian Eeg
Hestetun, Kjersti E
Dahl, Olav
Myklebust, Mette P
author_sort Jacob, Havjin
collection PubMed
description Despite advances in colon cancer research and novel therapies, high risk of recurrence remains a major challenge. This study reports miRNA expression profiling as a biomarker for the prognosis of TNM stage II and III colon cancer. Fresh frozen biopsies from the study cohort (N=111) were analyzed for miRNA by RT-qPCR and LASSO regression analysis was used to build a classifier of miRNAs. The prognostic accuracy was tested and the classifier was validated in an independent colon cohort (TCGA-COAD, N=209). The LASSO regression analysis identified a 16-miRNA signature including miR-143-5p, miR-27a-3p, miR-31-5p, miR-181a-5p, miR-30b-5p, miR-30d-5p, miR-146a-5p, miR-23a-3p, miR-150-5p, miR-210-3p, miR-25-3p, miR-196a-5p, miR-148a-3p, miR-222-3p, miR-30c-5p and miR-223-3p. A low 16-miRNA signature was associated with better 5-year disease-free survival (DFS) in the study cohort than a high signature (93 % versus 58 %; p< 0.001). The signature was an independent prognostic factor for better 5-year DFS in multivariate analyses (HR 21.4; 95% CI: 4.21-108.7; p< 0.001). The results in the validation cohort were consistent with the study cohort in univariate (77 % versus 65 %; p= 0.045) and multivariate analyses (HR 2.0; 95% CI: 1.04-3.89; p=0.039). We identified a 16-miRNA signature as a reliable prognostic biomarker for classification of colon cancer stage II and III patients into groups with low and high risk for recurrence.
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spelling pubmed-56756762017-11-18 Identification of a sixteen-microRNA signature as prognostic biomarker for stage II and III colon cancer Jacob, Havjin Stanisavljevic, Luka Storli, Kristian Eeg Hestetun, Kjersti E Dahl, Olav Myklebust, Mette P Oncotarget Research Paper Despite advances in colon cancer research and novel therapies, high risk of recurrence remains a major challenge. This study reports miRNA expression profiling as a biomarker for the prognosis of TNM stage II and III colon cancer. Fresh frozen biopsies from the study cohort (N=111) were analyzed for miRNA by RT-qPCR and LASSO regression analysis was used to build a classifier of miRNAs. The prognostic accuracy was tested and the classifier was validated in an independent colon cohort (TCGA-COAD, N=209). The LASSO regression analysis identified a 16-miRNA signature including miR-143-5p, miR-27a-3p, miR-31-5p, miR-181a-5p, miR-30b-5p, miR-30d-5p, miR-146a-5p, miR-23a-3p, miR-150-5p, miR-210-3p, miR-25-3p, miR-196a-5p, miR-148a-3p, miR-222-3p, miR-30c-5p and miR-223-3p. A low 16-miRNA signature was associated with better 5-year disease-free survival (DFS) in the study cohort than a high signature (93 % versus 58 %; p< 0.001). The signature was an independent prognostic factor for better 5-year DFS in multivariate analyses (HR 21.4; 95% CI: 4.21-108.7; p< 0.001). The results in the validation cohort were consistent with the study cohort in univariate (77 % versus 65 %; p= 0.045) and multivariate analyses (HR 2.0; 95% CI: 1.04-3.89; p=0.039). We identified a 16-miRNA signature as a reliable prognostic biomarker for classification of colon cancer stage II and III patients into groups with low and high risk for recurrence. Impact Journals LLC 2017-09-23 /pmc/articles/PMC5675676/ /pubmed/29152124 http://dx.doi.org/10.18632/oncotarget.21237 Text en Copyright: © 2017 Jacob et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Jacob, Havjin
Stanisavljevic, Luka
Storli, Kristian Eeg
Hestetun, Kjersti E
Dahl, Olav
Myklebust, Mette P
Identification of a sixteen-microRNA signature as prognostic biomarker for stage II and III colon cancer
title Identification of a sixteen-microRNA signature as prognostic biomarker for stage II and III colon cancer
title_full Identification of a sixteen-microRNA signature as prognostic biomarker for stage II and III colon cancer
title_fullStr Identification of a sixteen-microRNA signature as prognostic biomarker for stage II and III colon cancer
title_full_unstemmed Identification of a sixteen-microRNA signature as prognostic biomarker for stage II and III colon cancer
title_short Identification of a sixteen-microRNA signature as prognostic biomarker for stage II and III colon cancer
title_sort identification of a sixteen-microrna signature as prognostic biomarker for stage ii and iii colon cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5675676/
https://www.ncbi.nlm.nih.gov/pubmed/29152124
http://dx.doi.org/10.18632/oncotarget.21237
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