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Absolute quantification of cell-free microRNAs in cancer patients
The hypothesis to use microRNAs (miRNAs) circulating in the blood as cancer biomarkers was formulated some years ago based on promising initial results. After some exciting discoveries, however, it became evident that the accurate quantification of cell-free miRNAs was more challenging than expected...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546486/ https://www.ncbi.nlm.nih.gov/pubmed/26036630 |
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author | Ferracin, Manuela Lupini, Laura Salamon, Irene Saccenti, Elena Zanzi, Maria Vittoria Rocchi, Andrea Da Ros, Lucia Zagatti, Barbara Musa, Gentian Bassi, Cristian Mangolini, Alessandra Cavallesco, Giorgio Frassoldati, Antonio Volpato, Stefano Carcoforo, Paolo Hollingsworth, Alan B. Negrini, Massimo |
author_facet | Ferracin, Manuela Lupini, Laura Salamon, Irene Saccenti, Elena Zanzi, Maria Vittoria Rocchi, Andrea Da Ros, Lucia Zagatti, Barbara Musa, Gentian Bassi, Cristian Mangolini, Alessandra Cavallesco, Giorgio Frassoldati, Antonio Volpato, Stefano Carcoforo, Paolo Hollingsworth, Alan B. Negrini, Massimo |
author_sort | Ferracin, Manuela |
collection | PubMed |
description | The hypothesis to use microRNAs (miRNAs) circulating in the blood as cancer biomarkers was formulated some years ago based on promising initial results. After some exciting discoveries, however, it became evident that the accurate quantification of cell-free miRNAs was more challenging than expected. Difficulties were linked to the strong impact that many, if not all, pre- and post- analytical variables have on the final results. In this study, we used currently available high-throughput technologies to identify miRNAs present in plasma and serum of patients with breast, colorectal, lung, thyroid and melanoma tumors, and healthy controls. Then, we assessed the absolute level of nine different miRNAs (miR-320a, miR-21-5p, miR-378a-3p, miR-181a-5p, miR-3156-5p, miR-2110, miR-125a-5p, miR-425-5p, miR-766-3p) in 207 samples from healthy controls and cancer patients using droplet digital PCR (ddPCR) technology. We identified miRNAs specifically modulated in one or more cancer types, according to tissue source. The significant reduction of miR-181a-5p levels in breast cancer patients serum was further validated using two independent cohorts, one from Italy (n = 70) and one from US (n = 90), with AUC 0.66 and 0.73 respectively. This study finally powers the use of cell-free miRNAs as cancer biomarkers and propose miR-181a-5p as a diagnostic breast cancer biomarker. |
format | Online Article Text |
id | pubmed-4546486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-45464862015-08-27 Absolute quantification of cell-free microRNAs in cancer patients Ferracin, Manuela Lupini, Laura Salamon, Irene Saccenti, Elena Zanzi, Maria Vittoria Rocchi, Andrea Da Ros, Lucia Zagatti, Barbara Musa, Gentian Bassi, Cristian Mangolini, Alessandra Cavallesco, Giorgio Frassoldati, Antonio Volpato, Stefano Carcoforo, Paolo Hollingsworth, Alan B. Negrini, Massimo Oncotarget Research Paper The hypothesis to use microRNAs (miRNAs) circulating in the blood as cancer biomarkers was formulated some years ago based on promising initial results. After some exciting discoveries, however, it became evident that the accurate quantification of cell-free miRNAs was more challenging than expected. Difficulties were linked to the strong impact that many, if not all, pre- and post- analytical variables have on the final results. In this study, we used currently available high-throughput technologies to identify miRNAs present in plasma and serum of patients with breast, colorectal, lung, thyroid and melanoma tumors, and healthy controls. Then, we assessed the absolute level of nine different miRNAs (miR-320a, miR-21-5p, miR-378a-3p, miR-181a-5p, miR-3156-5p, miR-2110, miR-125a-5p, miR-425-5p, miR-766-3p) in 207 samples from healthy controls and cancer patients using droplet digital PCR (ddPCR) technology. We identified miRNAs specifically modulated in one or more cancer types, according to tissue source. The significant reduction of miR-181a-5p levels in breast cancer patients serum was further validated using two independent cohorts, one from Italy (n = 70) and one from US (n = 90), with AUC 0.66 and 0.73 respectively. This study finally powers the use of cell-free miRNAs as cancer biomarkers and propose miR-181a-5p as a diagnostic breast cancer biomarker. Impact Journals LLC 2015-05-02 /pmc/articles/PMC4546486/ /pubmed/26036630 Text en Copyright: © 2015 Ferracin et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Ferracin, Manuela Lupini, Laura Salamon, Irene Saccenti, Elena Zanzi, Maria Vittoria Rocchi, Andrea Da Ros, Lucia Zagatti, Barbara Musa, Gentian Bassi, Cristian Mangolini, Alessandra Cavallesco, Giorgio Frassoldati, Antonio Volpato, Stefano Carcoforo, Paolo Hollingsworth, Alan B. Negrini, Massimo Absolute quantification of cell-free microRNAs in cancer patients |
title | Absolute quantification of cell-free microRNAs in cancer patients |
title_full | Absolute quantification of cell-free microRNAs in cancer patients |
title_fullStr | Absolute quantification of cell-free microRNAs in cancer patients |
title_full_unstemmed | Absolute quantification of cell-free microRNAs in cancer patients |
title_short | Absolute quantification of cell-free microRNAs in cancer patients |
title_sort | absolute quantification of cell-free micrornas in cancer patients |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546486/ https://www.ncbi.nlm.nih.gov/pubmed/26036630 |
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