MicroRNA Profile in Peripheral Blood Mononuclear Cells from Hepatitis B Virus Infected Patients

Introduction and aim. The pathogenesis of hepatitis B virus (HBV)-related liver diseases remains not fully understood. Here, we aim to explore the potential roles of dysregulated miRNAs in chronic hepatitis B (CHB) and HBV-related acute-on-chronic liver failure (ACLF).Material and methods. MiRNA mic...

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Main Authors: Kangkang Yu, Qian Li, M.D., Ph.D., Ning Li
Format: Article
Language:English
Published: Elsevier 2018-11-01
Series:Annals of Hepatology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1665268119310634
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spelling doaj-f4637ba60c184c5ca8ac0955ae7fc4e12021-06-09T05:53:19ZengElsevierAnnals of Hepatology1665-26812018-11-0117610121020MicroRNA Profile in Peripheral Blood Mononuclear Cells from Hepatitis B Virus Infected PatientsKangkang Yu0Qian Li, M.D., Ph.D.1Ning Li2Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, ChinaDepartment of General Surgery, Qingdao Municipal Hospital, Qingdao, Shandong, China; Correspondence and reprint request:Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, ChinaIntroduction and aim. The pathogenesis of hepatitis B virus (HBV)-related liver diseases remains not fully understood. Here, we aim to explore the potential roles of dysregulated miRNAs in chronic hepatitis B (CHB) and HBV-related acute-on-chronic liver failure (ACLF).Material and methods. MiRNA microarray was conducted in peripheral blood mononuclear cells (PBMCs) obtained from healthy donors or patients with CHB or ACLF. Altered expression of miRNAs was further confirmed by quantitative real-time polymerase chain reaction (qRT-PCR) analysis. Finally, the differentially expressed miRNAs and their target genes were subjected to bioinformatics analysis.Results. The miRNA microarray identified 45 up-regulated and 62 down-regulated miRNAs with a fold change > 1.5. Expression of eight miRNAs was validated using qRT-PCR analysis, which was consistent with miRNA microarray analysis. Bioinformatics analysis indicated that multiple biological processes and signaling pathways were affected by these miRNAs and a miRNA-gene regulatory network was generated with Cytoscape.Conclusion. The current study provided a global view of miRNA expression in PBMCs from CHB and ACLF patients. Functional analysis showed that multiple biological processes and signaling pathways were modulated by these miRNAs. These data provide intriguing insights into the molecular pathogenesis of HBV-related liver diseases, which deserve further investigation.http://www.sciencedirect.com/science/article/pii/S1665268119310634Non-coding RNAChronic hepatitis BBioinformatics
collection DOAJ
language English
format Article
sources DOAJ
author Kangkang Yu
Qian Li, M.D., Ph.D.
Ning Li
spellingShingle Kangkang Yu
Qian Li, M.D., Ph.D.
Ning Li
MicroRNA Profile in Peripheral Blood Mononuclear Cells from Hepatitis B Virus Infected Patients
Annals of Hepatology
Non-coding RNA
Chronic hepatitis B
Bioinformatics
author_facet Kangkang Yu
Qian Li, M.D., Ph.D.
Ning Li
author_sort Kangkang Yu
title MicroRNA Profile in Peripheral Blood Mononuclear Cells from Hepatitis B Virus Infected Patients
title_short MicroRNA Profile in Peripheral Blood Mononuclear Cells from Hepatitis B Virus Infected Patients
title_full MicroRNA Profile in Peripheral Blood Mononuclear Cells from Hepatitis B Virus Infected Patients
title_fullStr MicroRNA Profile in Peripheral Blood Mononuclear Cells from Hepatitis B Virus Infected Patients
title_full_unstemmed MicroRNA Profile in Peripheral Blood Mononuclear Cells from Hepatitis B Virus Infected Patients
title_sort microrna profile in peripheral blood mononuclear cells from hepatitis b virus infected patients
publisher Elsevier
series Annals of Hepatology
issn 1665-2681
publishDate 2018-11-01
description Introduction and aim. The pathogenesis of hepatitis B virus (HBV)-related liver diseases remains not fully understood. Here, we aim to explore the potential roles of dysregulated miRNAs in chronic hepatitis B (CHB) and HBV-related acute-on-chronic liver failure (ACLF).Material and methods. MiRNA microarray was conducted in peripheral blood mononuclear cells (PBMCs) obtained from healthy donors or patients with CHB or ACLF. Altered expression of miRNAs was further confirmed by quantitative real-time polymerase chain reaction (qRT-PCR) analysis. Finally, the differentially expressed miRNAs and their target genes were subjected to bioinformatics analysis.Results. The miRNA microarray identified 45 up-regulated and 62 down-regulated miRNAs with a fold change > 1.5. Expression of eight miRNAs was validated using qRT-PCR analysis, which was consistent with miRNA microarray analysis. Bioinformatics analysis indicated that multiple biological processes and signaling pathways were affected by these miRNAs and a miRNA-gene regulatory network was generated with Cytoscape.Conclusion. The current study provided a global view of miRNA expression in PBMCs from CHB and ACLF patients. Functional analysis showed that multiple biological processes and signaling pathways were modulated by these miRNAs. These data provide intriguing insights into the molecular pathogenesis of HBV-related liver diseases, which deserve further investigation.
topic Non-coding RNA
Chronic hepatitis B
Bioinformatics
url http://www.sciencedirect.com/science/article/pii/S1665268119310634
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