Evidence map›Paper›PMID 40837640›Full record

ArticleAfrican health sciences2025

Expression levels and polymorphisms of the microRNA maturing components; diagnostic values of Drosha, DGCR8 and Dicer in patients with vitiligo.

Soner Aşır, Özlem İzci Ay, Mustafa Ertan Ay, Kenan Çevik, Gurbet Doğru Özdemir, Merve Türkegün Şengül, Mehmet Emin Erdal, Ümit Türsen

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Article in African health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Soner AşırMersin University, Faculty of Medicine, Department of Medical Biology and Genetics.
Özlem İzci AyMersin University, Faculty of Medicine, Department of Medical Biology and Genetics.
Mustafa Ertan AyMersin University, Faculty of Medicine, Department of Medical Biology and Genetics.
Kenan ÇevikMersin University, Faculty of Medicine, Department of Medical Biology and Genetics.
Gurbet Doğru ÖzdemirMersin University, Faculty of Medicine, Department of Medical Biology and Genetics.
Merve Türkegün ŞengülAlanya Alaaddin Keykubat University, Faculty of Medicine, Department of Biostatistics and Medical Informatics.
Mehmet Emin ErdalMersin University, Faculty of Medicine, Department of Medical Biology and Genetics.
Ümit TürsenMersin University, Faculty of Medicine, Department of Dermatology.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objective: Even though the pathogenesis of vitiligo is still unclear, recent studies have suggested that miRNAs can contribute to the occurrence and progression of the disease. The aim of the present study was to investigate the associations between SNPs of miRNA processing genes and their expression levels with vitiligo susceptibility. Methods: 55 patients and 56 controls were investigated for Dicer, Drosha, and DGCR8 gene expressions and genotyped for Drosha rs493760, DGCR8 rs1640299, and Dicer rs1057035 by real-time PCR. The correlation of the expression levels of these three genes was analyzed. The ROC curve was used to analyze their diagnostic efficacy for vitiligo. Results: The current findings showed that the Dicer CT genotype was more frequent in vitiligo (p=0.046) compared to controls, while Drosha and DGCR8 polymorphisms did not show significant associations. The relative expression levels of the three genes in vitiligo patients were significantly lower than those in the control group (p<0.05). The areas under the curves for Drosha, DGCR8, and Dicer were 0.969, 0.66, 0.67. Conclusions: For the first time, we demonstrate that the Dicer rs1057035 polymorphism is associated with vitiligo susceptibility, and the downregulation of Drosha, DGCR8, and Dicer suggests their potential roles as biomarkers in the pathogenesis of vitiligo.

Indexed as

DEAD-box RNA HelicasesMicroRNAsRibonuclease IIIRNA-Binding ProteinsVitiligoAdultCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedPolymorphism, Single NucleotideDEAD-box RNA HelicasesDGCR8 protein, humanDICER1 protein, humanDROSHA protein, humanMicroRNAsRibonuclease IIIRNA-Binding ProteinsDGCR8DicerDroshamiRNA biogenesisVitiligo

Identifiers

PMID40837640
PMCPMC12361973

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