Increased Expression of Plasma-Induced ABCC1 mRNA in Cystic Fibrosis
The gene is structurally and functionally related to the cystic fibrosis transmembrane conductance regulator gene ( ). Upregulation of is thought to improve lung function in patients with cystic fibrosis (CF); the mechanism underlying this effect is unknown. We analyzed the promoter single nucleotid...
Gespeichert in:
Veröffentlicht in: | International journal of molecular sciences 2017-08, Vol.18 (8), p.1752 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The
gene is structurally and functionally related to the cystic fibrosis transmembrane conductance regulator gene (
). Upregulation of
is thought to improve lung function in patients with cystic fibrosis (CF); the mechanism underlying this effect is unknown. We analyzed the
promoter single nucleotide polymorphism (SNP rs504348), plasma-induced
mRNA expression levels, and
methylation status and their correlation with clinical variables among CF subjects with differing
mutations. We assigned 93 CF subjects into disease severity groups and genotyped SNP rs504348. For 23 CF subjects and 7 healthy controls, donor peripheral blood mononuclear cells (PBMCs) stimulated with plasma underwent gene expression analysis via qRT-PCR.
promoter methylation was analyzed in the same 23 CF subjects. No significant correlation was observed between rs504348 genotypes and CF disease severity, but pancreatic insufficient CF subjects showed increased colonization with any form of
(OR = 3.125, 95% CI: 1.192-8.190) and mucoid
(OR = 5.075, 95% CI: 1.307-28.620) compared to the pancreatic sufficient group. A significantly higher expression of
mRNA was induced by CF plasma compared to healthy control plasma (
< 0.001). CF subjects with rs504348 (CC/CG) also had higher mRNA expression compared to those with the ancestral GG genotype (
< 0.005).
promoter was completely unmethylated; therefore, we did not detect any association between methylation and CF disease severity. In silico predictions suggested that histone modifications are crucial for regulating
expression in PBMCs. Our results suggest that
expression has a role in
activity thereby increasing our understanding of the molecular underpinnings of the clinical heterogeneity in CF. |
---|---|
ISSN: | 1422-0067 1661-6596 1422-0067 |
DOI: | 10.3390/ijms18081752 |