Expression profiling of miRNA-196a biomarker in naïve hepatitis C virus-infected and Sofosbuvir plus Daclatasvir-treated patients

被引:0
|
作者
Nazim Hussain
Nimrah Farooq
Muhammad Maqsood
Muhammad Shahid Riaz Rajoka
Muhammad Bilal
机构
[1] University of the Punjab,Centre for Applied Molecular Biology (CAMB)
[2] Lahore General Hospital,Department of Medicine
[3] Shenzhen University,Department of Food Science and Engineering, College of Chemistry and Chemical Engineering
[4] Huaiyin Institute of Technology,School of Life Science and Food Engineering
来源
Archives of Microbiology | 2021年 / 203卷
关键词
MiRNA-196a; Hepatitis C virus; Quantitative PCR; Therapeutics; Biomarker;
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学科分类号
摘要
Micro-RNA (miRNA) is a short stretch of nucleotides that can regulate many genes associated with the various stages of the hepatitis C virus (HCV) life cycle and disease progression. This study evaluates the expression profiling of miRNA-196a in naïve HCV-infected, and Sofosbuvir plus Daclatasvir-treated patients. MiRNA-196a can inhibit HCV replication by silencing the HCV NS5A protein or downregulating the human BACH-I mRNA. The expression level of miRNA-196a was determined by quantitative reverse transcription PCR (RT-qPCR) using the whole RNA extracted from the recruited participant’s serum. Results showed a 0.83-fold decrease in the miRNA-196a level in naïve HCV-infected than controls. On the contrary, an increase in the expression level by 0.06-fold was observed in Sofosbuvir plus Daclatasvir-treated patients. A negative but significant correlation was recorded between the HCV-RNA load and miRNA-196a expression level in the naïve-infected patients. Serum miRNA-196a ROC curve analysis revealed an area under the curve of 0.8278 (95% CI 0.7033–0.9524, p < 0.0001) with 82.05% sensitivity and 76.19% specificity in discriminating the healthy controls from the HCV-infected samples. In conclusion, our study explored the comparative expression levels of miRNA-196a in HCV-infected and Sofosbuvir plus Daclatasvir patients. Further studies are needed to examine the possible role of miR-196a as a therapeutic agent for treating HCV-infected patients.
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页码:2365 / 2371
页数:6
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