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Plasma microRNA panels to diagnose pancreatic cancer: Results from a multicenter study
Biomarkers for the early diagnosis of pancreatic cancer (PC) are urgent needed. Plasma microRNAs (miRNAs) might be used as biomarkers for the diagnosis of cancer. We analyzed 361 plasma samples from 6 surgical centers in China and performed machine learning approach. We gain insight of the associati...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173079/ https://www.ncbi.nlm.nih.gov/pubmed/27223429 http://dx.doi.org/10.18632/oncotarget.9491 |
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author | Cao, Zhe Liu, Chang Xu, Jianwei You, Lei Wang, Chunyou Lou, Wenhui Sun, Bei Miao, Yi Liu, Xubao Wang, Xiaowo Zhang, Taiping Zhao, Yupei |
author_facet | Cao, Zhe Liu, Chang Xu, Jianwei You, Lei Wang, Chunyou Lou, Wenhui Sun, Bei Miao, Yi Liu, Xubao Wang, Xiaowo Zhang, Taiping Zhao, Yupei |
author_sort | Cao, Zhe |
collection | PubMed |
description | Biomarkers for the early diagnosis of pancreatic cancer (PC) are urgent needed. Plasma microRNAs (miRNAs) might be used as biomarkers for the diagnosis of cancer. We analyzed 361 plasma samples from 6 surgical centers in China and performed machine learning approach. We gain insight of the association between the aberrant plasma miRNA expression and pancreatic disease. 671 microRNAs were screened in the discovery phase and 33 microRNAs in the training phase and 13 microRNAs in the validation phase. After the discovery phase and training phase, 2 diagnostic panels were constructed comprising 3 microRNAs in panel I (miR-486-5p, miR-126-3p, miR-106b-3p) and 6 microRNAs in panel II (miR-486-5p, miR-126-3p, miR-106b-3p, miR-938, miR-26b-3p, miR-1285). Panel I and panel II had high accuracy for distinguishing pancreatic cancer from chronic pancreatitis (CP) with area under the curve (AUC) values of 0.891 (Standard Error (SE): 0.097) and 0.889 (SE: 0.097) respectively, in the validation phase. Additionally, we demonstrated that the diagnostic value of the panels in discriminating PC from CP were comparable to that of carbohydrate antigen 19–9 (CA 19–9) 0.775 (SE: 0.053) (P = 0.1 for both). This study identified 2 diagnostic panels based on microRNA expression in plasma with the potential to distinguish PC from CP. These patterns might be developed as biomarkers for pancreatic cancer. |
format | Online Article Text |
id | pubmed-5173079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-51730792016-12-23 Plasma microRNA panels to diagnose pancreatic cancer: Results from a multicenter study Cao, Zhe Liu, Chang Xu, Jianwei You, Lei Wang, Chunyou Lou, Wenhui Sun, Bei Miao, Yi Liu, Xubao Wang, Xiaowo Zhang, Taiping Zhao, Yupei Oncotarget Research Paper Biomarkers for the early diagnosis of pancreatic cancer (PC) are urgent needed. Plasma microRNAs (miRNAs) might be used as biomarkers for the diagnosis of cancer. We analyzed 361 plasma samples from 6 surgical centers in China and performed machine learning approach. We gain insight of the association between the aberrant plasma miRNA expression and pancreatic disease. 671 microRNAs were screened in the discovery phase and 33 microRNAs in the training phase and 13 microRNAs in the validation phase. After the discovery phase and training phase, 2 diagnostic panels were constructed comprising 3 microRNAs in panel I (miR-486-5p, miR-126-3p, miR-106b-3p) and 6 microRNAs in panel II (miR-486-5p, miR-126-3p, miR-106b-3p, miR-938, miR-26b-3p, miR-1285). Panel I and panel II had high accuracy for distinguishing pancreatic cancer from chronic pancreatitis (CP) with area under the curve (AUC) values of 0.891 (Standard Error (SE): 0.097) and 0.889 (SE: 0.097) respectively, in the validation phase. Additionally, we demonstrated that the diagnostic value of the panels in discriminating PC from CP were comparable to that of carbohydrate antigen 19–9 (CA 19–9) 0.775 (SE: 0.053) (P = 0.1 for both). This study identified 2 diagnostic panels based on microRNA expression in plasma with the potential to distinguish PC from CP. These patterns might be developed as biomarkers for pancreatic cancer. Impact Journals LLC 2016-05-19 /pmc/articles/PMC5173079/ /pubmed/27223429 http://dx.doi.org/10.18632/oncotarget.9491 Text en Copyright: © 2016 Cao 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 Cao, Zhe Liu, Chang Xu, Jianwei You, Lei Wang, Chunyou Lou, Wenhui Sun, Bei Miao, Yi Liu, Xubao Wang, Xiaowo Zhang, Taiping Zhao, Yupei Plasma microRNA panels to diagnose pancreatic cancer: Results from a multicenter study |
title | Plasma microRNA panels to diagnose pancreatic cancer: Results from a multicenter study |
title_full | Plasma microRNA panels to diagnose pancreatic cancer: Results from a multicenter study |
title_fullStr | Plasma microRNA panels to diagnose pancreatic cancer: Results from a multicenter study |
title_full_unstemmed | Plasma microRNA panels to diagnose pancreatic cancer: Results from a multicenter study |
title_short | Plasma microRNA panels to diagnose pancreatic cancer: Results from a multicenter study |
title_sort | plasma microrna panels to diagnose pancreatic cancer: results from a multicenter study |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5173079/ https://www.ncbi.nlm.nih.gov/pubmed/27223429 http://dx.doi.org/10.18632/oncotarget.9491 |
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