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Novel blood-based microRNA biomarker panel for early diagnosis of chronic pancreatitis

Chronic pancreatitis (CP) is an inflammatory disease characterized by progressive fibrosis of pancreas. Early diagnosis will improve the prognosis of patients. This study aimed to obtain serum miRNA biomarkers for early diagnosis of CP. In the current study, we analyzed the differentially expressed...

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Autores principales: Xin, Lei, Gao, Jun, Wang, Dan, Lin, Jin-Huan, Liao, Zhuan, Ji, Jun-Tao, Du, Ting-Ting, Jiang, Fei, Hu, Liang-Hao, Li, Zhao-Shen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225423/
https://www.ncbi.nlm.nih.gov/pubmed/28074846
http://dx.doi.org/10.1038/srep40019
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author Xin, Lei
Gao, Jun
Wang, Dan
Lin, Jin-Huan
Liao, Zhuan
Ji, Jun-Tao
Du, Ting-Ting
Jiang, Fei
Hu, Liang-Hao
Li, Zhao-Shen
author_facet Xin, Lei
Gao, Jun
Wang, Dan
Lin, Jin-Huan
Liao, Zhuan
Ji, Jun-Tao
Du, Ting-Ting
Jiang, Fei
Hu, Liang-Hao
Li, Zhao-Shen
author_sort Xin, Lei
collection PubMed
description Chronic pancreatitis (CP) is an inflammatory disease characterized by progressive fibrosis of pancreas. Early diagnosis will improve the prognosis of patients. This study aimed to obtain serum miRNA biomarkers for early diagnosis of CP. In the current study, we analyzed the differentially expressed miRNAs (DEmiRs) of CP patients from Gene Expression Omnibus (GEO), and the DEmiRs in plasma of early CP patients (n = 10) from clinic by miRNA microarrays. Expression levels of DEmiRs were further tested in clinical samples including early CP patients (n = 20), late CP patients (n = 20) and healthy controls (n = 18). The primary endpoints were area under curve (AUC) and expression levels of DEmiRs. Four DEmiRs (hsa-miR-320a-d) were obtained from GEO CP, meanwhile two (hsa-miR-221 and hsa-miR-130a) were identified as distinct biomarkers of early CP by miRNA microarrays. When applied on clinical serum samples, hsa-miR-320a-d were accurate in predicting late CP, while hsa-miR-221 and hsa-miR-130a were accurate in predicting early CP with AUC of 100.0% and 87.5%. Our study indicates that miRNA expression profile is different in early and late CP. Hsa-miR-221 and hsa-miR-130a are biomarkers of early CP, and the panel of the above 6 serum miRNAs has the potential to be applied clinically for early diagnosis of CP.
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spelling pubmed-52254232017-01-17 Novel blood-based microRNA biomarker panel for early diagnosis of chronic pancreatitis Xin, Lei Gao, Jun Wang, Dan Lin, Jin-Huan Liao, Zhuan Ji, Jun-Tao Du, Ting-Ting Jiang, Fei Hu, Liang-Hao Li, Zhao-Shen Sci Rep Article Chronic pancreatitis (CP) is an inflammatory disease characterized by progressive fibrosis of pancreas. Early diagnosis will improve the prognosis of patients. This study aimed to obtain serum miRNA biomarkers for early diagnosis of CP. In the current study, we analyzed the differentially expressed miRNAs (DEmiRs) of CP patients from Gene Expression Omnibus (GEO), and the DEmiRs in plasma of early CP patients (n = 10) from clinic by miRNA microarrays. Expression levels of DEmiRs were further tested in clinical samples including early CP patients (n = 20), late CP patients (n = 20) and healthy controls (n = 18). The primary endpoints were area under curve (AUC) and expression levels of DEmiRs. Four DEmiRs (hsa-miR-320a-d) were obtained from GEO CP, meanwhile two (hsa-miR-221 and hsa-miR-130a) were identified as distinct biomarkers of early CP by miRNA microarrays. When applied on clinical serum samples, hsa-miR-320a-d were accurate in predicting late CP, while hsa-miR-221 and hsa-miR-130a were accurate in predicting early CP with AUC of 100.0% and 87.5%. Our study indicates that miRNA expression profile is different in early and late CP. Hsa-miR-221 and hsa-miR-130a are biomarkers of early CP, and the panel of the above 6 serum miRNAs has the potential to be applied clinically for early diagnosis of CP. Nature Publishing Group 2017-01-11 /pmc/articles/PMC5225423/ /pubmed/28074846 http://dx.doi.org/10.1038/srep40019 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Xin, Lei
Gao, Jun
Wang, Dan
Lin, Jin-Huan
Liao, Zhuan
Ji, Jun-Tao
Du, Ting-Ting
Jiang, Fei
Hu, Liang-Hao
Li, Zhao-Shen
Novel blood-based microRNA biomarker panel for early diagnosis of chronic pancreatitis
title Novel blood-based microRNA biomarker panel for early diagnosis of chronic pancreatitis
title_full Novel blood-based microRNA biomarker panel for early diagnosis of chronic pancreatitis
title_fullStr Novel blood-based microRNA biomarker panel for early diagnosis of chronic pancreatitis
title_full_unstemmed Novel blood-based microRNA biomarker panel for early diagnosis of chronic pancreatitis
title_short Novel blood-based microRNA biomarker panel for early diagnosis of chronic pancreatitis
title_sort novel blood-based microrna biomarker panel for early diagnosis of chronic pancreatitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5225423/
https://www.ncbi.nlm.nih.gov/pubmed/28074846
http://dx.doi.org/10.1038/srep40019
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