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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Mazandaran University of Medical Sciences and Health Services
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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 |
work_keys_str_mv |
AT zahraazhir differentialexpressionofmir18binpbmcfromt1dpatientsinisfahanpopulation AT zohrehhojati differentialexpressionofmir18binpbmcfromt1dpatientsinisfahanpopulation |
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