Turkish journal of medical sciences · 2025
miRNA-target gene network analysis in siblings with cystic fibrosis and phenotypic variability.
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Mustafaoğlu Ayberk, Noyan Senem, Akkaya Ulum Yeliz Z, Gür Dedeoğlu Bala, Emiralioğlu Nagehan, Özçelik Uğur, Yalçin Ebru, Doğru Deniz, Kiper Nural, Dayangaç Erden Didem
Аннотация
BACKGROUND/AIM: Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. CF is characterized by respiratory tract infections, pancreatic insufficiency, meconium ileus, intestinal obstruction, and male infertility. A genotype to phenotype correlation is difficult to establish because of the heterogeneity of disease severity. Even patients with the same CFTR mutation can have varying clinical severities. In recent years, studies have explored the role of microRNA (miRNA) expression in the regulation of respiratory diseases. However, no research has been conducted to date on miRNAs in siblings with the same CFTR mutation.
MATERIALS AND METHODS: Nasal cells of CF siblings from two families with discordant phenotype (n = 2 per family) were collected, and differentially expressed miRNAs were identified using miRNA arrays. Differentially expressed miRNAs and their target genes were determined using several bioinformatic databases and tools.
RESULTS: miR-449c-5p, miR-92b-3p, miR-34c-3p, miR-34c-5p, miR-6732-5p, and miR-4793-3p were differentially expressed in patients with severe disease compared to mild. CXCL1, CXCL2, DUSP1, GCLC, ICAM1, KIT, PRKAA2, and PTGS2 genes were identified as the target genes of candidate miRNAs (miR-34c-3p, miR-92b-3p, miR-449c-5p, miR-4793-3p). miRNA-mRNA interaction network analysis was performed and strong interaction was shown between miR-449c-5p target genes (CXCL1, CXCL2, PTGS2, ICAM1). CXCL1 expression decreased 5.28-fold in patients with severe disease compared to those with mild (p = 0.01).
CONCLUSION: Our results highlight the importance of miR-449c-5p interaction with CXCL1 and other target genes related to inflammation. Further studies should focus on the functional analysis of miR-449c-5p.
MATERIALS AND METHODS: Nasal cells of CF siblings from two families with discordant phenotype (n = 2 per family) were collected, and differentially expressed miRNAs were identified using miRNA arrays. Differentially expressed miRNAs and their target genes were determined using several bioinformatic databases and tools.
RESULTS: miR-449c-5p, miR-92b-3p, miR-34c-3p, miR-34c-5p, miR-6732-5p, and miR-4793-3p were differentially expressed in patients with severe disease compared to mild. CXCL1, CXCL2, DUSP1, GCLC, ICAM1, KIT, PRKAA2, and PTGS2 genes were identified as the target genes of candidate miRNAs (miR-34c-3p, miR-92b-3p, miR-449c-5p, miR-4793-3p). miRNA-mRNA interaction network analysis was performed and strong interaction was shown between miR-449c-5p target genes (CXCL1, CXCL2, PTGS2, ICAM1). CXCL1 expression decreased 5.28-fold in patients with severe disease compared to those with mild (p = 0.01).
CONCLUSION: Our results highlight the importance of miR-449c-5p interaction with CXCL1 and other target genes related to inflammation. Further studies should focus on the functional analysis of miR-449c-5p.