Cargando…

Identification of potential microRNA panels for pancreatic cancer diagnosis using microarray datasets and bioinformatics methods

Pancreatic cancer (PC) is a malignancy with little/no warning signs before the disease reaches its ultimate stages. Currently early detection of PC is very difficult because most patients have non-specific symptoms leading to postponing the correct diagnosis. In this study, using multiple bioinforma...

Descripción completa

Detalles Bibliográficos
Autores principales: Shams, Roshanak, Saberi, Samaneh, Zali, Mohammadreza, Sadeghi, Amir, Ghafouri-Fard, Soudeh, Aghdaei, Hamid Asadzadeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200710/
https://www.ncbi.nlm.nih.gov/pubmed/32371926
http://dx.doi.org/10.1038/s41598-020-64569-1
_version_ 1783529393609506816
author Shams, Roshanak
Saberi, Samaneh
Zali, Mohammadreza
Sadeghi, Amir
Ghafouri-Fard, Soudeh
Aghdaei, Hamid Asadzadeh
author_facet Shams, Roshanak
Saberi, Samaneh
Zali, Mohammadreza
Sadeghi, Amir
Ghafouri-Fard, Soudeh
Aghdaei, Hamid Asadzadeh
author_sort Shams, Roshanak
collection PubMed
description Pancreatic cancer (PC) is a malignancy with little/no warning signs before the disease reaches its ultimate stages. Currently early detection of PC is very difficult because most patients have non-specific symptoms leading to postponing the correct diagnosis. In this study, using multiple bioinformatics tools, we integrated various serum expression profiles of miRNAs to find the most significant miRNA signatures helpful in diagnosis of PC and constructed novel miRNA diagnosis models for PC. Altogether, 27 differentially expressed miRNAs (DEMs) showed area under curve (AUC) score >80%. The most promising miRNAs, miR-1469 and miR-4530, were individually able to distinguish two groups with the highest specificity and sensitivity. By using multivariate cox regression analyses, 5 diagnostic models consisting of different combinations of miRNAs, based on their significant expression algorithms and functional properties were introduced. The correlation model consisting of miR-125a-3p, miR-5100 and miR-642b-3p was the most promising model in the diagnosis of PC patients from healthy controls with an AUC of 0.95, Sensitivity 0.98 and Specificity 0.97. Validation analysis was conducted for considered miRNAs on a final cohort consist of the microarray data from two other datasets (GSE112264 & GSE124158) . These results provide some potential biomarkers for PC diagnosis after testing in large case-control and cohort studies.
format Online
Article
Text
id pubmed-7200710
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-72007102020-05-12 Identification of potential microRNA panels for pancreatic cancer diagnosis using microarray datasets and bioinformatics methods Shams, Roshanak Saberi, Samaneh Zali, Mohammadreza Sadeghi, Amir Ghafouri-Fard, Soudeh Aghdaei, Hamid Asadzadeh Sci Rep Article Pancreatic cancer (PC) is a malignancy with little/no warning signs before the disease reaches its ultimate stages. Currently early detection of PC is very difficult because most patients have non-specific symptoms leading to postponing the correct diagnosis. In this study, using multiple bioinformatics tools, we integrated various serum expression profiles of miRNAs to find the most significant miRNA signatures helpful in diagnosis of PC and constructed novel miRNA diagnosis models for PC. Altogether, 27 differentially expressed miRNAs (DEMs) showed area under curve (AUC) score >80%. The most promising miRNAs, miR-1469 and miR-4530, were individually able to distinguish two groups with the highest specificity and sensitivity. By using multivariate cox regression analyses, 5 diagnostic models consisting of different combinations of miRNAs, based on their significant expression algorithms and functional properties were introduced. The correlation model consisting of miR-125a-3p, miR-5100 and miR-642b-3p was the most promising model in the diagnosis of PC patients from healthy controls with an AUC of 0.95, Sensitivity 0.98 and Specificity 0.97. Validation analysis was conducted for considered miRNAs on a final cohort consist of the microarray data from two other datasets (GSE112264 & GSE124158) . These results provide some potential biomarkers for PC diagnosis after testing in large case-control and cohort studies. Nature Publishing Group UK 2020-05-05 /pmc/articles/PMC7200710/ /pubmed/32371926 http://dx.doi.org/10.1038/s41598-020-64569-1 Text en © The Author(s) 2020 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
Shams, Roshanak
Saberi, Samaneh
Zali, Mohammadreza
Sadeghi, Amir
Ghafouri-Fard, Soudeh
Aghdaei, Hamid Asadzadeh
Identification of potential microRNA panels for pancreatic cancer diagnosis using microarray datasets and bioinformatics methods
title Identification of potential microRNA panels for pancreatic cancer diagnosis using microarray datasets and bioinformatics methods
title_full Identification of potential microRNA panels for pancreatic cancer diagnosis using microarray datasets and bioinformatics methods
title_fullStr Identification of potential microRNA panels for pancreatic cancer diagnosis using microarray datasets and bioinformatics methods
title_full_unstemmed Identification of potential microRNA panels for pancreatic cancer diagnosis using microarray datasets and bioinformatics methods
title_short Identification of potential microRNA panels for pancreatic cancer diagnosis using microarray datasets and bioinformatics methods
title_sort identification of potential microrna panels for pancreatic cancer diagnosis using microarray datasets and bioinformatics methods
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7200710/
https://www.ncbi.nlm.nih.gov/pubmed/32371926
http://dx.doi.org/10.1038/s41598-020-64569-1
work_keys_str_mv AT shamsroshanak identificationofpotentialmicrornapanelsforpancreaticcancerdiagnosisusingmicroarraydatasetsandbioinformaticsmethods
AT saberisamaneh identificationofpotentialmicrornapanelsforpancreaticcancerdiagnosisusingmicroarraydatasetsandbioinformaticsmethods
AT zalimohammadreza identificationofpotentialmicrornapanelsforpancreaticcancerdiagnosisusingmicroarraydatasetsandbioinformaticsmethods
AT sadeghiamir identificationofpotentialmicrornapanelsforpancreaticcancerdiagnosisusingmicroarraydatasetsandbioinformaticsmethods
AT ghafourifardsoudeh identificationofpotentialmicrornapanelsforpancreaticcancerdiagnosisusingmicroarraydatasetsandbioinformaticsmethods
AT aghdaeihamidasadzadeh identificationofpotentialmicrornapanelsforpancreaticcancerdiagnosisusingmicroarraydatasetsandbioinformaticsmethods