Differential Expression of MiR-18b in PBMC from T1D Patients in Isfahan population

Background: Type 1 diabetes (T1D) is caused by cell-mediated autoimmune attack on pancreatic beta-cells. Previous studies highlight the role of microRNAs (miRNAs) in the pathogenesis of T1D. MiRNAs are small non-coding RNAs involved in the regulation of gene expression post-transcriptionally. In thi...

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Main Authors: Zahra Azhir, Zohreh Hojati
Format: Article
Language:English
Published: Mazandaran University of Medical Sciences and Health Services 2016-11-01
Series:Research in Molecular Medicine
Subjects:
Online Access:http://rmm.mazums.ac.ir/browse.php?a_code=A-10-691-4&slc_lang=en&sid=1
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spelling doaj-f30baeedc07a43a3aded57a880dccde82020-11-25T03:45:17ZengMazandaran University of Medical Sciences and Health ServicesResearch in Molecular Medicine2322-13482322-133X2016-11-01444550Differential Expression of MiR-18b in PBMC from T1D Patients in Isfahan populationZahra Azhir0Zohreh Hojati1 Division of Genetics, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran. Division of Genetics, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran. Background: Type 1 diabetes (T1D) is caused by cell-mediated autoimmune attack on pancreatic beta-cells. Previous studies highlight the role of microRNAs (miRNAs) in the pathogenesis of T1D. MiRNAs are small non-coding RNAs involved in the regulation of gene expression post-transcriptionally. In this work, miR-18b was chosen and the differential expression of it was measured between T1D patients and healthy controls from Isfahan population. Materials and Methods: MiR-18b was selected using Bioinformatics studies by miRWalk software. 22 T1D patients and 18 healthy controls from Isfahan population were enrolled in this study. Total RNA of the peripheral blood mononuclear cells (PBMCs) samples were extracted. After cDNA synthesis, the expression profile of miR-18b quantified by means of qPCR method in patients and controls. Finally the results were statistically analyzed. Results: In this study despite our hypothesis, the expression levels of miR-18b didn’t show any significant difference between T1D patients and healthy controls (p value: 0.145). Conclusion: Due to the results of our experimental analysis, it seems that miR-18b doesn’t have any association with T1D disease in Isfahan population.http://rmm.mazums.ac.ir/browse.php?a_code=A-10-691-4&slc_lang=en&sid=1type 1 diabetes (T1D) microRNA miR-18b qPCR miRWalk
collection DOAJ
language English
format Article
sources DOAJ
author Zahra Azhir
Zohreh Hojati
spellingShingle Zahra Azhir
Zohreh Hojati
Differential Expression of MiR-18b in PBMC from T1D Patients in Isfahan population
Research in Molecular Medicine
type 1 diabetes (T1D)
microRNA
miR-18b
qPCR
miRWalk
author_facet Zahra Azhir
Zohreh Hojati
author_sort Zahra Azhir
title Differential Expression of MiR-18b in PBMC from T1D Patients in Isfahan population
title_short Differential Expression of MiR-18b in PBMC from T1D Patients in Isfahan population
title_full Differential Expression of MiR-18b in PBMC from T1D Patients in Isfahan population
title_fullStr Differential Expression of MiR-18b in PBMC from T1D Patients in Isfahan population
title_full_unstemmed Differential Expression of MiR-18b in PBMC from T1D Patients in Isfahan population
title_sort differential expression of mir-18b in pbmc from t1d patients in isfahan population
publisher Mazandaran University of Medical Sciences and Health Services
series Research in Molecular Medicine
issn 2322-1348
2322-133X
publishDate 2016-11-01
description Background: Type 1 diabetes (T1D) is caused by cell-mediated autoimmune attack on pancreatic beta-cells. Previous studies highlight the role of microRNAs (miRNAs) in the pathogenesis of T1D. MiRNAs are small non-coding RNAs involved in the regulation of gene expression post-transcriptionally. In this work, miR-18b was chosen and the differential expression of it was measured between T1D patients and healthy controls from Isfahan population. Materials and Methods: MiR-18b was selected using Bioinformatics studies by miRWalk software. 22 T1D patients and 18 healthy controls from Isfahan population were enrolled in this study. Total RNA of the peripheral blood mononuclear cells (PBMCs) samples were extracted. After cDNA synthesis, the expression profile of miR-18b quantified by means of qPCR method in patients and controls. Finally the results were statistically analyzed. Results: In this study despite our hypothesis, the expression levels of miR-18b didn’t show any significant difference between T1D patients and healthy controls (p value: 0.145). Conclusion: Due to the results of our experimental analysis, it seems that miR-18b doesn’t have any association with T1D disease in Isfahan population.
topic type 1 diabetes (T1D)
microRNA
miR-18b
qPCR
miRWalk
url http://rmm.mazums.ac.ir/browse.php?a_code=A-10-691-4&slc_lang=en&sid=1
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