MicroRNA expression profiles and type 1 diabetes mellitus: systematic review and bioinformatic analysis

Growing evidence indicates that microRNAs (miRNAs) have a key role in processes involved in type 1 diabetes mellitus (T1DM) pathogenesis, including immune system functions and beta-cell metabolism and death. Although dysregulated miRNA profiles have been identified in T1DM patients, results are inc...

Full description

Bibliographic Details
Main Authors: Taís S Assmann, Mariana Recamonde-Mendoza, Bianca M De Souza, Daisy Crispim
Format: Article
Language:English
Published: Bioscientifica 2017-11-01
Series:Endocrine Connections
Subjects:
Online Access:http://www.endocrineconnections.com/content/6/8/773.full
_version_ 1811205038391951360
author Taís S Assmann
Mariana Recamonde-Mendoza
Bianca M De Souza
Daisy Crispim
author_facet Taís S Assmann
Mariana Recamonde-Mendoza
Bianca M De Souza
Daisy Crispim
author_sort Taís S Assmann
collection DOAJ
description Growing evidence indicates that microRNAs (miRNAs) have a key role in processes involved in type 1 diabetes mellitus (T1DM) pathogenesis, including immune system functions and beta-cell metabolism and death. Although dysregulated miRNA profiles have been identified in T1DM patients, results are inconclusive; with only few miRNAs being consistently dysregulated among studies. Thus, we performed a systematic review of the literature on the subject, followed by bioinformatic analysis, to point out which miRNAs are dysregulated in T1DM-related tissues and in which pathways they act. PubMed and EMBASE were searched to identify all studies that compared miRNA expressions between T1DM patients and non-diabetic controls. Search was completed in August, 2017. Those miRNAs consistently dysregulated in T1DM-related tissues were submitted to bioinformatic analysis, using six databases of miRNA–target gene interactions to retrieve their putative targets and identify potentially affected pathways under their regulation. Thirty-three studies were included in the systematic review: 19 of them reported miRNA expressions in human samples, 13 in murine models and one in both human and murine samples. Among 278 dysregulated miRNAs reported in these studies, 25.9% were reported in at least 2 studies; however, only 48 of them were analyzed in tissues directly related to T1DM pathogenesis (serum/plasma, pancreas and peripheral blood mononuclear cells (PBMCs)). Regarding circulating miRNAs, 11 were consistently dysregulated in T1DM patients compared to controls: miR-21-5p, miR-24-3p, miR-100-5p, miR-146a-5p, miR-148a-3p, miR-150-5p, miR-181a-5p, miR-210-5p, miR-342-3p, miR-375 and miR-1275. The bioinformatic analysis retrieved a total of 5867 validated and 2979 predicted miRNA–target interactions for human miRNAs. In functional enrichment analysis of miRNA target genes, 77 KEGG terms were enriched for more than one miRNA. These miRNAs are involved in pathways related to immune system function, cell survival, cell proliferation and insulin biosynthesis and secretion. In conclusion, eleven circulating miRNAs seem to be dysregulated in T1DM patients in different studies, being potential circulating biomarkers of this disease.
first_indexed 2024-04-12T03:23:52Z
format Article
id doaj.art-4990f78cb4a345748060363f6fa6bcd6
institution Directory Open Access Journal
issn 2049-3614
2049-3614
language English
last_indexed 2024-04-12T03:23:52Z
publishDate 2017-11-01
publisher Bioscientifica
record_format Article
series Endocrine Connections
spelling doaj.art-4990f78cb4a345748060363f6fa6bcd62022-12-22T03:49:48ZengBioscientificaEndocrine Connections2049-36142049-36142017-11-016877379010.1530/EC-17-0248MicroRNA expression profiles and type 1 diabetes mellitus: systematic review and bioinformatic analysisTaís S Assmann0Mariana Recamonde-Mendoza1Bianca M De Souza2Daisy Crispim3Endocrine Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil; Postgraduation Program in Medical Sciences: Endocrinology, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, BrazilInstitute of Informatics, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, BrazilEndocrine Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil; Postgraduation Program in Medical Sciences: Endocrinology, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, BrazilEndocrine Division, Hospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil; Postgraduation Program in Medical Sciences: Endocrinology, Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, BrazilGrowing evidence indicates that microRNAs (miRNAs) have a key role in processes involved in type 1 diabetes mellitus (T1DM) pathogenesis, including immune system functions and beta-cell metabolism and death. Although dysregulated miRNA profiles have been identified in T1DM patients, results are inconclusive; with only few miRNAs being consistently dysregulated among studies. Thus, we performed a systematic review of the literature on the subject, followed by bioinformatic analysis, to point out which miRNAs are dysregulated in T1DM-related tissues and in which pathways they act. PubMed and EMBASE were searched to identify all studies that compared miRNA expressions between T1DM patients and non-diabetic controls. Search was completed in August, 2017. Those miRNAs consistently dysregulated in T1DM-related tissues were submitted to bioinformatic analysis, using six databases of miRNA–target gene interactions to retrieve their putative targets and identify potentially affected pathways under their regulation. Thirty-three studies were included in the systematic review: 19 of them reported miRNA expressions in human samples, 13 in murine models and one in both human and murine samples. Among 278 dysregulated miRNAs reported in these studies, 25.9% were reported in at least 2 studies; however, only 48 of them were analyzed in tissues directly related to T1DM pathogenesis (serum/plasma, pancreas and peripheral blood mononuclear cells (PBMCs)). Regarding circulating miRNAs, 11 were consistently dysregulated in T1DM patients compared to controls: miR-21-5p, miR-24-3p, miR-100-5p, miR-146a-5p, miR-148a-3p, miR-150-5p, miR-181a-5p, miR-210-5p, miR-342-3p, miR-375 and miR-1275. The bioinformatic analysis retrieved a total of 5867 validated and 2979 predicted miRNA–target interactions for human miRNAs. In functional enrichment analysis of miRNA target genes, 77 KEGG terms were enriched for more than one miRNA. These miRNAs are involved in pathways related to immune system function, cell survival, cell proliferation and insulin biosynthesis and secretion. In conclusion, eleven circulating miRNAs seem to be dysregulated in T1DM patients in different studies, being potential circulating biomarkers of this disease.http://www.endocrineconnections.com/content/6/8/773.fullsystematic reviewmicroRNAtype 1 diabetes mellitusbioinformatic analysis
spellingShingle Taís S Assmann
Mariana Recamonde-Mendoza
Bianca M De Souza
Daisy Crispim
MicroRNA expression profiles and type 1 diabetes mellitus: systematic review and bioinformatic analysis
Endocrine Connections
systematic review
microRNA
type 1 diabetes mellitus
bioinformatic analysis
title MicroRNA expression profiles and type 1 diabetes mellitus: systematic review and bioinformatic analysis
title_full MicroRNA expression profiles and type 1 diabetes mellitus: systematic review and bioinformatic analysis
title_fullStr MicroRNA expression profiles and type 1 diabetes mellitus: systematic review and bioinformatic analysis
title_full_unstemmed MicroRNA expression profiles and type 1 diabetes mellitus: systematic review and bioinformatic analysis
title_short MicroRNA expression profiles and type 1 diabetes mellitus: systematic review and bioinformatic analysis
title_sort microrna expression profiles and type 1 diabetes mellitus systematic review and bioinformatic analysis
topic systematic review
microRNA
type 1 diabetes mellitus
bioinformatic analysis
url http://www.endocrineconnections.com/content/6/8/773.full
work_keys_str_mv AT taissassmann micrornaexpressionprofilesandtype1diabetesmellitussystematicreviewandbioinformaticanalysis
AT marianarecamondemendoza micrornaexpressionprofilesandtype1diabetesmellitussystematicreviewandbioinformaticanalysis
AT biancamdesouza micrornaexpressionprofilesandtype1diabetesmellitussystematicreviewandbioinformaticanalysis
AT daisycrispim micrornaexpressionprofilesandtype1diabetesmellitussystematicreviewandbioinformaticanalysis