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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...

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Autores principales: Cao, Zhe, Liu, Chang, Xu, Jianwei, You, Lei, Wang, Chunyou, Lou, Wenhui, Sun, Bei, Miao, Yi, Liu, Xubao, Wang, Xiaowo, Zhang, Taiping, Zhao, Yupei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
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.
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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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