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Alcohol accumulation promotes esophagitis via pyroptosis activation

Gastroesophageal reflux impairs the mucosal barrier in the distal esophagus, allowing chronic exposure of the squamous epithelium to multitudinous stimulations and inducing chronic inflammation. Esophagitis is a response to inflammation of the esophageal squamous mucosa. Our study clarified that alc...

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Autores principales: Wang, Fengjiao, Li, Gang, Ning, Jinfeng, Chen, Lantao, Xu, Hai, Kong, Xianglong, Bu, Jianlong, Zhao, Weiwei, Li, Zhengtian, Wang, Xiuyun, Li, Xiaoguang, Ma, Jianqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097477/
https://www.ncbi.nlm.nih.gov/pubmed/30123073
http://dx.doi.org/10.7150/ijbs.24347
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author Wang, Fengjiao
Li, Gang
Ning, Jinfeng
Chen, Lantao
Xu, Hai
Kong, Xianglong
Bu, Jianlong
Zhao, Weiwei
Li, Zhengtian
Wang, Xiuyun
Li, Xiaoguang
Ma, Jianqun
author_facet Wang, Fengjiao
Li, Gang
Ning, Jinfeng
Chen, Lantao
Xu, Hai
Kong, Xianglong
Bu, Jianlong
Zhao, Weiwei
Li, Zhengtian
Wang, Xiuyun
Li, Xiaoguang
Ma, Jianqun
author_sort Wang, Fengjiao
collection PubMed
description Gastroesophageal reflux impairs the mucosal barrier in the distal esophagus, allowing chronic exposure of the squamous epithelium to multitudinous stimulations and inducing chronic inflammation. Esophagitis is a response to inflammation of the esophageal squamous mucosa. Our study clarified that alcohol accumulation could aggravate the progress of esophagitis by inducing pyroptosis; however, Ac-YVAD-CMK, an inhibitor of caspase-1, could effectively suppress the expression of IL-1β and IL-18 both in vivo and in vitro, reducing the inflammatory response, which is promised to be an agent to inhibit the progression of esophagitis. Additionally, caspase-1-derived pyroptosis is involved in esophageal cancer.
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spelling pubmed-60974772018-08-17 Alcohol accumulation promotes esophagitis via pyroptosis activation Wang, Fengjiao Li, Gang Ning, Jinfeng Chen, Lantao Xu, Hai Kong, Xianglong Bu, Jianlong Zhao, Weiwei Li, Zhengtian Wang, Xiuyun Li, Xiaoguang Ma, Jianqun Int J Biol Sci Research Paper Gastroesophageal reflux impairs the mucosal barrier in the distal esophagus, allowing chronic exposure of the squamous epithelium to multitudinous stimulations and inducing chronic inflammation. Esophagitis is a response to inflammation of the esophageal squamous mucosa. Our study clarified that alcohol accumulation could aggravate the progress of esophagitis by inducing pyroptosis; however, Ac-YVAD-CMK, an inhibitor of caspase-1, could effectively suppress the expression of IL-1β and IL-18 both in vivo and in vitro, reducing the inflammatory response, which is promised to be an agent to inhibit the progression of esophagitis. Additionally, caspase-1-derived pyroptosis is involved in esophageal cancer. Ivyspring International Publisher 2018-07-13 /pmc/articles/PMC6097477/ /pubmed/30123073 http://dx.doi.org/10.7150/ijbs.24347 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Wang, Fengjiao
Li, Gang
Ning, Jinfeng
Chen, Lantao
Xu, Hai
Kong, Xianglong
Bu, Jianlong
Zhao, Weiwei
Li, Zhengtian
Wang, Xiuyun
Li, Xiaoguang
Ma, Jianqun
Alcohol accumulation promotes esophagitis via pyroptosis activation
title Alcohol accumulation promotes esophagitis via pyroptosis activation
title_full Alcohol accumulation promotes esophagitis via pyroptosis activation
title_fullStr Alcohol accumulation promotes esophagitis via pyroptosis activation
title_full_unstemmed Alcohol accumulation promotes esophagitis via pyroptosis activation
title_short Alcohol accumulation promotes esophagitis via pyroptosis activation
title_sort alcohol accumulation promotes esophagitis via pyroptosis activation
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097477/
https://www.ncbi.nlm.nih.gov/pubmed/30123073
http://dx.doi.org/10.7150/ijbs.24347
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