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Reference miRNAs for colorectal cancer: analysis and verification of current data

MicroRNAs (miRNAs) hold great promise in cancer research. The use of appropriate reference miRNAs for normalization of qPCR data is crucial for accurate expression analysis. We present here analysis and verification of current data, proposing a workflow strategy for identification of reference miRNA...

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Autores principales: Danese, E., Minicozzi, A. M, Benati, M., Paviati, E., Lima-Oliveira, G., Gusella, M., Pasini, F., Salvagno, G. L, Montagnana, M., Lippi, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567181/
https://www.ncbi.nlm.nih.gov/pubmed/28827728
http://dx.doi.org/10.1038/s41598-017-08784-3
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author Danese, E.
Minicozzi, A. M
Benati, M.
Paviati, E.
Lima-Oliveira, G.
Gusella, M.
Pasini, F.
Salvagno, G. L
Montagnana, M.
Lippi, G.
author_facet Danese, E.
Minicozzi, A. M
Benati, M.
Paviati, E.
Lima-Oliveira, G.
Gusella, M.
Pasini, F.
Salvagno, G. L
Montagnana, M.
Lippi, G.
author_sort Danese, E.
collection PubMed
description MicroRNAs (miRNAs) hold great promise in cancer research. The use of appropriate reference miRNAs for normalization of qPCR data is crucial for accurate expression analysis. We present here analysis and verification of current data, proposing a workflow strategy for identification of reference miRNAs in colorectal cancer (CRC). We performed a systematic review of studies aimed to identify stable reference miRNAs in CRC through high-throughput screening. Among the candidate miRNAs selected from the literature we excluded those predicted to target oncogenes or tumor suppressor gene. We then assessed the expression levels of the remaining candidates in exosomes, plasma and tissue samples from CRC patients and healthy controls. The expression stability was evaluated by box-plot, ∆Cq analysis, NormFinder and BestKeeper statistical algorithms. The effects of normalisers on the relative quantification of the oncogenic miR-1290 was also assessed. Our results consistently showed that different combinations of miR-520d, miR-1228 and miR-345 provided the most stably expressed reference miRNAs in the three biological matrices. We identified suitable reference miRNAs for future miRNA expression studies in exosomes plasma and tissues CRC samples. We also provided a novel conceptual framework that overcome the need of performing ex novo identification of suitable reference genes in single experimental systems.
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spelling pubmed-55671812017-09-01 Reference miRNAs for colorectal cancer: analysis and verification of current data Danese, E. Minicozzi, A. M Benati, M. Paviati, E. Lima-Oliveira, G. Gusella, M. Pasini, F. Salvagno, G. L Montagnana, M. Lippi, G. Sci Rep Article MicroRNAs (miRNAs) hold great promise in cancer research. The use of appropriate reference miRNAs for normalization of qPCR data is crucial for accurate expression analysis. We present here analysis and verification of current data, proposing a workflow strategy for identification of reference miRNAs in colorectal cancer (CRC). We performed a systematic review of studies aimed to identify stable reference miRNAs in CRC through high-throughput screening. Among the candidate miRNAs selected from the literature we excluded those predicted to target oncogenes or tumor suppressor gene. We then assessed the expression levels of the remaining candidates in exosomes, plasma and tissue samples from CRC patients and healthy controls. The expression stability was evaluated by box-plot, ∆Cq analysis, NormFinder and BestKeeper statistical algorithms. The effects of normalisers on the relative quantification of the oncogenic miR-1290 was also assessed. Our results consistently showed that different combinations of miR-520d, miR-1228 and miR-345 provided the most stably expressed reference miRNAs in the three biological matrices. We identified suitable reference miRNAs for future miRNA expression studies in exosomes plasma and tissues CRC samples. We also provided a novel conceptual framework that overcome the need of performing ex novo identification of suitable reference genes in single experimental systems. Nature Publishing Group UK 2017-08-21 /pmc/articles/PMC5567181/ /pubmed/28827728 http://dx.doi.org/10.1038/s41598-017-08784-3 Text en © The Author(s) 2017 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
Danese, E.
Minicozzi, A. M
Benati, M.
Paviati, E.
Lima-Oliveira, G.
Gusella, M.
Pasini, F.
Salvagno, G. L
Montagnana, M.
Lippi, G.
Reference miRNAs for colorectal cancer: analysis and verification of current data
title Reference miRNAs for colorectal cancer: analysis and verification of current data
title_full Reference miRNAs for colorectal cancer: analysis and verification of current data
title_fullStr Reference miRNAs for colorectal cancer: analysis and verification of current data
title_full_unstemmed Reference miRNAs for colorectal cancer: analysis and verification of current data
title_short Reference miRNAs for colorectal cancer: analysis and verification of current data
title_sort reference mirnas for colorectal cancer: analysis and verification of current data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5567181/
https://www.ncbi.nlm.nih.gov/pubmed/28827728
http://dx.doi.org/10.1038/s41598-017-08784-3
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