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Plasma Micro-RNA Alterations Appear Late in Pancreatic Cancer

OBJECTIVES: The aim of this research was to study whether plasma microRNAs (miRNA) can be used for early detection of pancreatic cancer (PC) by analyzing prediagnostic plasma samples collected before a PC diagnosis. BACKGROUND: PC has a poor prognosis due to late presenting symptoms and early metast...

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Autores principales: Franklin, Oskar, Jonsson, Pär, Billing, Ola, Lundberg, Erik, Öhlund, Daniel, Nyström, Hanna, Lundin, Christina, Antti, Henrik, Sund, Malin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott, Williams, and Wilkins 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865497/
https://www.ncbi.nlm.nih.gov/pubmed/28425921
http://dx.doi.org/10.1097/SLA.0000000000002124
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author Franklin, Oskar
Jonsson, Pär
Billing, Ola
Lundberg, Erik
Öhlund, Daniel
Nyström, Hanna
Lundin, Christina
Antti, Henrik
Sund, Malin
author_facet Franklin, Oskar
Jonsson, Pär
Billing, Ola
Lundberg, Erik
Öhlund, Daniel
Nyström, Hanna
Lundin, Christina
Antti, Henrik
Sund, Malin
author_sort Franklin, Oskar
collection PubMed
description OBJECTIVES: The aim of this research was to study whether plasma microRNAs (miRNA) can be used for early detection of pancreatic cancer (PC) by analyzing prediagnostic plasma samples collected before a PC diagnosis. BACKGROUND: PC has a poor prognosis due to late presenting symptoms and early metastasis. Circulating miRNAs are altered in PC at diagnosis but have not been evaluated in a prediagnostic setting. METHODS: We first performed an initial screen using a panel of 372 miRNAs in a retrospective case-control cohort that included early-stage PC patients and healthy controls. Significantly altered miRNAs at diagnosis were then measured in an early detection case-control cohort wherein plasma samples in the cases are collected before a PC diagnosis. Carbohydrate antigen 19–9 (Ca 19–9) levels were measured in all samples for comparison. RESULTS: Our initial screen, including 23 stage I-II PC cases and 22 controls, revealed 15 candidate miRNAs that were differentially expressed in plasma samples at PC diagnosis. We combined all 15 miRNAs into a multivariate statistical model, which outperformed Ca 19–9 in receiver-operating characteristics analysis. However, none of the candidate miRNAs, individually or in combination, were significantly altered in prediagnostic plasma samples from 67 future PC patients compared with 132 matched controls. In comparison, Ca 19–9 levels were significantly higher in the cases at <5 years before diagnosis. CONCLUSION: Plasma miRNAs are altered in PC patients at diagnosis, but the candidate miRNAs found in this study appear late in the course of the disease and cannot be used for early detection of the disease.
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spelling pubmed-58654972018-04-04 Plasma Micro-RNA Alterations Appear Late in Pancreatic Cancer Franklin, Oskar Jonsson, Pär Billing, Ola Lundberg, Erik Öhlund, Daniel Nyström, Hanna Lundin, Christina Antti, Henrik Sund, Malin Ann Surg Original Articles OBJECTIVES: The aim of this research was to study whether plasma microRNAs (miRNA) can be used for early detection of pancreatic cancer (PC) by analyzing prediagnostic plasma samples collected before a PC diagnosis. BACKGROUND: PC has a poor prognosis due to late presenting symptoms and early metastasis. Circulating miRNAs are altered in PC at diagnosis but have not been evaluated in a prediagnostic setting. METHODS: We first performed an initial screen using a panel of 372 miRNAs in a retrospective case-control cohort that included early-stage PC patients and healthy controls. Significantly altered miRNAs at diagnosis were then measured in an early detection case-control cohort wherein plasma samples in the cases are collected before a PC diagnosis. Carbohydrate antigen 19–9 (Ca 19–9) levels were measured in all samples for comparison. RESULTS: Our initial screen, including 23 stage I-II PC cases and 22 controls, revealed 15 candidate miRNAs that were differentially expressed in plasma samples at PC diagnosis. We combined all 15 miRNAs into a multivariate statistical model, which outperformed Ca 19–9 in receiver-operating characteristics analysis. However, none of the candidate miRNAs, individually or in combination, were significantly altered in prediagnostic plasma samples from 67 future PC patients compared with 132 matched controls. In comparison, Ca 19–9 levels were significantly higher in the cases at <5 years before diagnosis. CONCLUSION: Plasma miRNAs are altered in PC patients at diagnosis, but the candidate miRNAs found in this study appear late in the course of the disease and cannot be used for early detection of the disease. Lippincott, Williams, and Wilkins 2018-04 2017-01-03 /pmc/articles/PMC5865497/ /pubmed/28425921 http://dx.doi.org/10.1097/SLA.0000000000002124 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Original Articles
Franklin, Oskar
Jonsson, Pär
Billing, Ola
Lundberg, Erik
Öhlund, Daniel
Nyström, Hanna
Lundin, Christina
Antti, Henrik
Sund, Malin
Plasma Micro-RNA Alterations Appear Late in Pancreatic Cancer
title Plasma Micro-RNA Alterations Appear Late in Pancreatic Cancer
title_full Plasma Micro-RNA Alterations Appear Late in Pancreatic Cancer
title_fullStr Plasma Micro-RNA Alterations Appear Late in Pancreatic Cancer
title_full_unstemmed Plasma Micro-RNA Alterations Appear Late in Pancreatic Cancer
title_short Plasma Micro-RNA Alterations Appear Late in Pancreatic Cancer
title_sort plasma micro-rna alterations appear late in pancreatic cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865497/
https://www.ncbi.nlm.nih.gov/pubmed/28425921
http://dx.doi.org/10.1097/SLA.0000000000002124
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