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Droplet digital PCR quantification of miR-1290 as a circulating biomarker for pancreatic cancer
Droplet digital PCR was used to validate miR-1290 as circulating biomarker for pancreatic cancer (PC). The diagnostic performance of miR-1290 was evaluate in 167 PC patients and 267 healthy subjects at clinical risk of developing the disease (HS). MiR-1290 plasma levels were compared to CA 19-9 dete...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219528/ https://www.ncbi.nlm.nih.gov/pubmed/30401891 http://dx.doi.org/10.1038/s41598-018-34597-z |
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author | Tavano, Francesca Gioffreda, Domenica Valvano, Maria R. Palmieri, Orazio Tardio, Matteo Latiano, Tiziana P. Piepoli, Ada Maiello, Evaristo Pirozzi, Felice Andriulli, Angelo |
author_facet | Tavano, Francesca Gioffreda, Domenica Valvano, Maria R. Palmieri, Orazio Tardio, Matteo Latiano, Tiziana P. Piepoli, Ada Maiello, Evaristo Pirozzi, Felice Andriulli, Angelo |
author_sort | Tavano, Francesca |
collection | PubMed |
description | Droplet digital PCR was used to validate miR-1290 as circulating biomarker for pancreatic cancer (PC). The diagnostic performance of miR-1290 was evaluate in 167 PC patients and 267 healthy subjects at clinical risk of developing the disease (HS). MiR-1290 plasma levels were compared to CA 19-9 determinations, and the combination of the two biomarkers was also taken into account. Plasma levels of miR-1290 were higher in PC patients compared to HS (p = 2.55 × 10(−16)). A similar trend was observed for CA 19-9 determinations (p = 1.03 × 10(−47)). ROC curve analysis revealed that miR-1290 in combination with CA 19-9 was effective for discriminating between PC patients and HS (AUC = 0.956, 95% CI = 0.933–0.979) than the two biomarkers tested alone (miR-1290: AUC = 0.734, 0.678–0.789; CA 19-9: AUC = 0.914, 0.877–0.951). The discriminating ability was higher when only PC patients with low or slightly increased CA 19-9 levels were compared with HS. MiR-1290 concentrations were not able to differentiate between PC patients with single or multiple risk factors for developing PC. Our data suggest that the absolute quantification of circulating miR-1290 levels does not allow to select patients at clinical risk of PC for entry into a surveillance program, and underline the methodological challenges still existing in utilizing circulating miRNAs as new promising biomarkers for PC. |
format | Online Article Text |
id | pubmed-6219528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62195282018-11-07 Droplet digital PCR quantification of miR-1290 as a circulating biomarker for pancreatic cancer Tavano, Francesca Gioffreda, Domenica Valvano, Maria R. Palmieri, Orazio Tardio, Matteo Latiano, Tiziana P. Piepoli, Ada Maiello, Evaristo Pirozzi, Felice Andriulli, Angelo Sci Rep Article Droplet digital PCR was used to validate miR-1290 as circulating biomarker for pancreatic cancer (PC). The diagnostic performance of miR-1290 was evaluate in 167 PC patients and 267 healthy subjects at clinical risk of developing the disease (HS). MiR-1290 plasma levels were compared to CA 19-9 determinations, and the combination of the two biomarkers was also taken into account. Plasma levels of miR-1290 were higher in PC patients compared to HS (p = 2.55 × 10(−16)). A similar trend was observed for CA 19-9 determinations (p = 1.03 × 10(−47)). ROC curve analysis revealed that miR-1290 in combination with CA 19-9 was effective for discriminating between PC patients and HS (AUC = 0.956, 95% CI = 0.933–0.979) than the two biomarkers tested alone (miR-1290: AUC = 0.734, 0.678–0.789; CA 19-9: AUC = 0.914, 0.877–0.951). The discriminating ability was higher when only PC patients with low or slightly increased CA 19-9 levels were compared with HS. MiR-1290 concentrations were not able to differentiate between PC patients with single or multiple risk factors for developing PC. Our data suggest that the absolute quantification of circulating miR-1290 levels does not allow to select patients at clinical risk of PC for entry into a surveillance program, and underline the methodological challenges still existing in utilizing circulating miRNAs as new promising biomarkers for PC. Nature Publishing Group UK 2018-11-06 /pmc/articles/PMC6219528/ /pubmed/30401891 http://dx.doi.org/10.1038/s41598-018-34597-z Text en © The Author(s) 2018 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 Tavano, Francesca Gioffreda, Domenica Valvano, Maria R. Palmieri, Orazio Tardio, Matteo Latiano, Tiziana P. Piepoli, Ada Maiello, Evaristo Pirozzi, Felice Andriulli, Angelo Droplet digital PCR quantification of miR-1290 as a circulating biomarker for pancreatic cancer |
title | Droplet digital PCR quantification of miR-1290 as a circulating biomarker for pancreatic cancer |
title_full | Droplet digital PCR quantification of miR-1290 as a circulating biomarker for pancreatic cancer |
title_fullStr | Droplet digital PCR quantification of miR-1290 as a circulating biomarker for pancreatic cancer |
title_full_unstemmed | Droplet digital PCR quantification of miR-1290 as a circulating biomarker for pancreatic cancer |
title_short | Droplet digital PCR quantification of miR-1290 as a circulating biomarker for pancreatic cancer |
title_sort | droplet digital pcr quantification of mir-1290 as a circulating biomarker for pancreatic cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219528/ https://www.ncbi.nlm.nih.gov/pubmed/30401891 http://dx.doi.org/10.1038/s41598-018-34597-z |
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