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Effects of Wnt signaling on epithelial to mesenchymal transition in chronic rhinosinusitis with nasal polyp.
- Source :
-
Thorax [Thorax] 2020 Nov; Vol. 75 (11), pp. 982-993. Date of Electronic Publication: 2020 Oct 06. - Publication Year :
- 2020
-
Abstract
- Background: Epithelial to mesenchymal transition (EMT) is associated with the pathophysiology of chronic rhinosinusitis with nasal polyp (CRSwNP). Wnt signaling is causative for EMT, whereas the mechanism in CRSwNP is not fully understood.<br />Objective: We sought to evaluate the role of Wnt signaling in EMT of CRSwNP using a murine nasal polyp (NP) model and human tissues.<br />Methods: Inflammatory markers and EMT-related molecules were evaluated in NP models using adenomatosis polyposis coli (Apc) <superscript>Min/+</superscript> mice with activated Wnt signaling and NP models treated with Wnt signaling inhibitor, indocyanine green-001 (ICG-001). EMT markers and Wnt signaling-associated mediators were analysed using human sinonasal tissues from control subjects and CRSwNP patients.<br />Results: Apc <superscript>Min/+</superscript> mice-induced NPs exhibited more frequent polypoid lesions and upregulation of Wnt-related molecules, including nuclear β-catenin, WNT3A and cyclin D1. Markers of EMT were significantly overexpressed in the Apc <superscript>Min/+</superscript> NP mice (p<0.001 for E-cadherin and α-smooth muscle actin), and interleukin (IL)-17A <superscript>+</superscript> cells and neutrophilic infiltration were increased in Apc <superscript>Min/+</superscript> NP mice (p<0.001). Inhibition of Wnt signaling via ICG-001 resulted in significantly decreased nasal polypoid lesions (p<0.001), EMT-related markers (p=0.019 for E-cadherin and p=0.002 for vimentin) and the mRNA levels of IL-4 (p<0.001) and IL-17A (p=0.004) compared with the positive control group. Finally, nuclear β-catenin (p=0.042) was significantly increased compared with the control, and the expression levels of Wnt ligands and receptors were upregulated in human NP tissues (p=0.045 for WNT3A and p=0.042 for FZD2), suggesting increased Wnt signaling and EMT in CRSwNP.<br />Conclusion: Wnt signaling may contribute to the pathogenesis of NPs through EMT. Therefore, inhibition of Wnt signaling may be a potential therapeutic strategy for patients with CRSwNP.<br />Competing Interests: Competing interests: None declared.<br /> (© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.)
- Subjects :
- Actins metabolism
Adenomatous Polyposis Coli Protein
Animals
Biomarkers metabolism
Cadherins metabolism
Cyclin D1 metabolism
Disease Models, Animal
Humans
Indocyanine Green pharmacology
Mice
Nasal Polyps drug therapy
Twist-Related Protein 1 metabolism
Up-Regulation
beta Catenin metabolism
Epithelial-Mesenchymal Transition physiology
Nasal Polyps physiopathology
Rhinitis physiopathology
Sinusitis physiopathology
Wnt Signaling Pathway physiology
Subjects
Details
- Language :
- English
- ISSN :
- 1468-3296
- Volume :
- 75
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Thorax
- Publication Type :
- Academic Journal
- Accession number :
- 33023995
- Full Text :
- https://doi.org/10.1136/thoraxjnl-2019-213916