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العنوان
MicroRNA expression as a predictor of the success of pegylated interferon-ribavirin therapy against chronic hepatitis C in Egyptian patients /
الناشر
Mahmoud Ahmed Senousy Hassan Ali ,
المؤلف
Mahmoud Ahmed Senousy Hassan Ali
هيئة الاعداد
باحث / Mahmoud Ahmed Senousy Hassan Ali
مشرف / Tarek Mohamed Kamal Motawi
مشرف / Shohda Assem Elmaraghy
مشرف / Olfat Gamil Shaker
تاريخ النشر
2016
عدد الصفحات
129 P. :
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
صيدلة
تاريخ الإجازة
9/3/2016
مكان الإجازة
جامعة القاهرة - كلية الصيدلة - Biochemistry
الفهرس
Only 14 pages are availabe for public view

from 161

from 161

Abstract

MicroRNAs (miRNAs) are messengers during interferon (IFN) virus interplay and are involved in antiviral immunity, however, little is known about IFN related miRNAs regarding their detection in serum and their potential use as non invasive diagnostic and prognostic biomarkers in chronic hepatitis C (CHC). Elucidate some of the molecular aspects underlying failure of pegylated IFN (PegIFN)-Ü/ribavirin (RBV) combination therapy, the present study investigated pretreatment expression profiles of seven selected IFN related miRNAs (miR- 146a, miR-34a, miR-130a, miR-19a, miR-192, miR-195, and miR-296) by quantitative reverse transcriptase polymerase chain reaction (RT-PCR) custom array technology in serum of Egyptian CHC patients with genotype 4 and whether their pretreatment levels would predict patient response to the combination therapy. One hundred and six CHC patients and forty age and sex- matched healthy controls were included. CHC patients were treated with standard PegIFN-Ü2b / RBV therapy and according to the virological response; they were divided into sustained virological response (SVR) and non-responder (NR) groups. Serum miR-34a, miR-130a, miR-19a, miR-192, miR-195, and miR-296 were upregulated, whereas serum miR-146a was downregulated in CHC patients compared to healthy controls. Significant correlations were found between relative expression levels of studied miRNAs and also with clinical data in CHC group. Pretreatment levels of serum miR-34a, miR-130a, and miR-195 were significantly higher, whereas miR-192 and miR-296 levels were significantly lower in SVR than NR patients