Circulating miRNAs as Predictor Markers for Activation of Hepatic Stellate Cells and Progression of HCV-Induced Liver Fibrosis

Introduction: Liver fibrosis is the excessive accumulation of extracellular matrix that occurs by activation of hepatic stellate cells (HSCs), which has been identified as the major driver of liver fibrosis. Several studies confirmed that miRNAs have regulatory effects on the activation of HSCs by...

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Main Authors: Eman El-Ahwany, Faten Nagy, Mona Zoheiry, Mohamed Shemis, Mona Nosseir, Hoda Abu Taleb, Maged El Ghannam, Rafaat Atta, Suher Zada
Format: Article
Language:English
Published: Electronic Physician 2016-01-01
Series:Electronic Physician
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Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768932/
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author Eman El-Ahwany
Faten Nagy
Mona Zoheiry
Mohamed Shemis
Mona Nosseir
Hoda Abu Taleb
Maged El Ghannam
Rafaat Atta
Suher Zada
Suher Zada
author_facet Eman El-Ahwany
Faten Nagy
Mona Zoheiry
Mohamed Shemis
Mona Nosseir
Hoda Abu Taleb
Maged El Ghannam
Rafaat Atta
Suher Zada
Suher Zada
author_sort Eman El-Ahwany
collection DOAJ
description Introduction: Liver fibrosis is the excessive accumulation of extracellular matrix that occurs by activation of hepatic stellate cells (HSCs), which has been identified as the major driver of liver fibrosis. Several studies confirmed that miRNAs have regulatory effects on the activation of HSCs by affecting the signaling pathways. The aim of this study was to develop non-invasive diagnostic markers by measuring different circulating miRNAs in serum as predictor markers for early diagnosis of liver fibrosis and its progression. Methods: In this case-control study, we enrolled 66 subjects with chronic hepatitis C (CHC) with early stage of fibrosis and 65 subjects with CHC with late-stage fibrosis. Also, 40 subjects were included as normal controls. The six main miRNAs, i.e., miR-138, miR-140, miR-143, miR-325, miR-328, and miR-349, were measured using the reverse transcription-polymerase chain reaction. Results: In the cases of CHC both with early and late stage of fibrosis, the circulating levels of the six main miRNAs were significantly higher than the levels in the control group. ROC analysis indicated that the sensitivity and specificity of miR-138 were 89.3% and 71.43%, respectively, in the early stage of fibrosis. In the late stage, the sensitivity and specificity of miR-138 were 89.3 and 93.02%, respectively, whereas, for miR-143, they were 75.0 and 88.4%, respectively. Conclusions: Circulating miR-138 could serve as a non-invasive biomarker for the detection of early fibrosis. Also, miR-138 and miR-143 could be specific biomarkers for indicating the late stage of liver fibrosis
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spelling doaj.art-e6338e3555bd46238fdd41e0c3cf48742022-12-21T19:02:28ZengElectronic PhysicianElectronic Physician2008-58422008-58422016-01-01811804181010.19082/1804Circulating miRNAs as Predictor Markers for Activation of Hepatic Stellate Cells and Progression of HCV-Induced Liver FibrosisEman El-AhwanyFaten NagyMona ZoheiryMohamed ShemisMona NosseirHoda Abu TalebMaged El GhannamRafaat AttaSuher ZadaSuher ZadaIntroduction: Liver fibrosis is the excessive accumulation of extracellular matrix that occurs by activation of hepatic stellate cells (HSCs), which has been identified as the major driver of liver fibrosis. Several studies confirmed that miRNAs have regulatory effects on the activation of HSCs by affecting the signaling pathways. The aim of this study was to develop non-invasive diagnostic markers by measuring different circulating miRNAs in serum as predictor markers for early diagnosis of liver fibrosis and its progression. Methods: In this case-control study, we enrolled 66 subjects with chronic hepatitis C (CHC) with early stage of fibrosis and 65 subjects with CHC with late-stage fibrosis. Also, 40 subjects were included as normal controls. The six main miRNAs, i.e., miR-138, miR-140, miR-143, miR-325, miR-328, and miR-349, were measured using the reverse transcription-polymerase chain reaction. Results: In the cases of CHC both with early and late stage of fibrosis, the circulating levels of the six main miRNAs were significantly higher than the levels in the control group. ROC analysis indicated that the sensitivity and specificity of miR-138 were 89.3% and 71.43%, respectively, in the early stage of fibrosis. In the late stage, the sensitivity and specificity of miR-138 were 89.3 and 93.02%, respectively, whereas, for miR-143, they were 75.0 and 88.4%, respectively. Conclusions: Circulating miR-138 could serve as a non-invasive biomarker for the detection of early fibrosis. Also, miR-138 and miR-143 could be specific biomarkers for indicating the late stage of liver fibrosishttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768932/liver fibrosismicroRNAschronic hepatitis C
spellingShingle Eman El-Ahwany
Faten Nagy
Mona Zoheiry
Mohamed Shemis
Mona Nosseir
Hoda Abu Taleb
Maged El Ghannam
Rafaat Atta
Suher Zada
Suher Zada
Circulating miRNAs as Predictor Markers for Activation of Hepatic Stellate Cells and Progression of HCV-Induced Liver Fibrosis
Electronic Physician
liver fibrosis
microRNAs
chronic hepatitis C
title Circulating miRNAs as Predictor Markers for Activation of Hepatic Stellate Cells and Progression of HCV-Induced Liver Fibrosis
title_full Circulating miRNAs as Predictor Markers for Activation of Hepatic Stellate Cells and Progression of HCV-Induced Liver Fibrosis
title_fullStr Circulating miRNAs as Predictor Markers for Activation of Hepatic Stellate Cells and Progression of HCV-Induced Liver Fibrosis
title_full_unstemmed Circulating miRNAs as Predictor Markers for Activation of Hepatic Stellate Cells and Progression of HCV-Induced Liver Fibrosis
title_short Circulating miRNAs as Predictor Markers for Activation of Hepatic Stellate Cells and Progression of HCV-Induced Liver Fibrosis
title_sort circulating mirnas as predictor markers for activation of hepatic stellate cells and progression of hcv induced liver fibrosis
topic liver fibrosis
microRNAs
chronic hepatitis C
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768932/
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