Positive Feedback Loop of SNAIL-IL-6 Mediates Myofibroblastic Differentiation Activity in Precancerous Oral Submucous Fibrosis.

Snail arecoline interleukin-6 myofibroblast oral submucosal fibrosis

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
18 Jun 2020
Historique:
received: 17 05 2020
revised: 11 06 2020
accepted: 11 06 2020
entrez: 24 6 2020
pubmed: 24 6 2020
medline: 24 6 2020
Statut: epublish

Résumé

Oral submucosal fibrosis (OSF) is a premalignant disorder of the oral cavity, and areca nut chewing is known to be a major etiological factor that could induce epithelial to mesenchymal transition (EMT) and activate buccal mucosal fibroblasts (BMFs). However, this detailed mechanism is not fully understood. In this study, we showed that the upregulation of Snail in OSF samples and fibrotic BMFs (fBMFs) may result from constant irritation by arecoline, a major alkaloid of the areca nut. The elevation of Snail triggered myofibroblast transdifferentiation and was crucial to the persistent activation of fBMFs. Meanwhile, Snail increased the expression of numerous fibrosis factors (e.g., α-SMA and collagen I) as well as IL-6. Results from bioinformatics software and a luciferase-based reporter assay revealed that IL-6 was a direct target of Snail. Moreover, IL-6 in BMFs was found to further increase the expression of Snail and mediate Snail-induced myofibroblast activation. These findings suggested that there was a positive loop between Snail and IL-6 to regulate the areca nut-associated myofibroblast transdifferentiation, which implied that the blockage of Snail may serve as a favorable therapeutic strategy for OSF treatment.

Identifiants

pubmed: 32570756
pii: cancers12061611
doi: 10.3390/cancers12061611
pmc: PMC7352888
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Chung Shan Medical University Hospital
ID : CSH-2018-C-013

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Auteurs

Chih-Yu Peng (CY)

School of Dentistry, Chung Shan Medical University, Taichung 40201, Taiwan.
Department of Dentistry, Chung Shan Medical University Hospital, Taichung 40201, Taiwan.

Yi-Wen Liao (YW)

School of Dentistry, Chung Shan Medical University, Taichung 40201, Taiwan.
Department of Dentistry, Chung Shan Medical University Hospital, Taichung 40201, Taiwan.

Ming-Yi Lu (MY)

School of Dentistry, Chung Shan Medical University, Taichung 40201, Taiwan.
Department of Dentistry, Chung Shan Medical University Hospital, Taichung 40201, Taiwan.

Chieh-Mei Yang (CM)

School of Dentistry, Chung Shan Medical University, Taichung 40201, Taiwan.

Pei-Ling Hsieh (PL)

Department of Anatomy, School of Medicine, China Medical University, Taichung 40402, Taiwan.

Cheng-Chia Yu (CC)

School of Dentistry, Chung Shan Medical University, Taichung 40201, Taiwan.
Department of Dentistry, Chung Shan Medical University Hospital, Taichung 40201, Taiwan.
Institute of Oral Sciences, Chung Shan Medical University, Taichung 40201, Taiwan.

Classifications MeSH