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Barretts's carcinogenesis
Barrett's esophagus is considered a precancerous lesion of esophageal adenocarcinoma (EAC). Long‐segment Barrett's esophagus, which is generally associated with intestinal metaplasia, has a higher rate of carcinogenesis than short‐segment Barrett's esophagus, which is mainly composed...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851828/ https://www.ncbi.nlm.nih.gov/pubmed/31290583 http://dx.doi.org/10.1111/pin.12804 |
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author | Mukaisho, Ken‐ichi Kanai, Shunpei Kushima, Ryoji Nakayama, Takahisa Hattori, Takanori Sugihara, Hiroyuki |
author_facet | Mukaisho, Ken‐ichi Kanai, Shunpei Kushima, Ryoji Nakayama, Takahisa Hattori, Takanori Sugihara, Hiroyuki |
author_sort | Mukaisho, Ken‐ichi |
collection | PubMed |
description | Barrett's esophagus is considered a precancerous lesion of esophageal adenocarcinoma (EAC). Long‐segment Barrett's esophagus, which is generally associated with intestinal metaplasia, has a higher rate of carcinogenesis than short‐segment Barrett's esophagus, which is mainly composed of cardiac‐type mucosa. However, a large number of cases reportedly develop EAC from the cardiac‐type mucosa which has the potential to involve intestinal phenotypes. There is no consensus regarding whether the definition of Barrett's epithelium should include intestinal metaplasia. Basic researches using rodent models have provided information regarding the origins of Barrett's epithelium. Nevertheless, it remains unclear whether differentiated gastric columnar epithelium or stratified esophageal squamous epithelium undergo transdifferentiation into the intestinal‐type columnar epithelium, transcommittment into the columnar epithelium, or whether the other pathways exist. Reflux of duodenal fluid including bile acids into the stomach may occur when an individual lies down after eating, which could cause the digestive juices to collect in the fornix of the stomach. N‐nitroso‐bile acids are produced with nitrites that are secreted from the salivary glands, and bile acids can drive expression of pro‐inflammatory cytokines via EGFR or the NF‐κB pathway. These steps may contribute significantly to carcinogenesis. |
format | Online Article Text |
id | pubmed-6851828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68518282019-11-18 Barretts's carcinogenesis Mukaisho, Ken‐ichi Kanai, Shunpei Kushima, Ryoji Nakayama, Takahisa Hattori, Takanori Sugihara, Hiroyuki Pathol Int Review Article Barrett's esophagus is considered a precancerous lesion of esophageal adenocarcinoma (EAC). Long‐segment Barrett's esophagus, which is generally associated with intestinal metaplasia, has a higher rate of carcinogenesis than short‐segment Barrett's esophagus, which is mainly composed of cardiac‐type mucosa. However, a large number of cases reportedly develop EAC from the cardiac‐type mucosa which has the potential to involve intestinal phenotypes. There is no consensus regarding whether the definition of Barrett's epithelium should include intestinal metaplasia. Basic researches using rodent models have provided information regarding the origins of Barrett's epithelium. Nevertheless, it remains unclear whether differentiated gastric columnar epithelium or stratified esophageal squamous epithelium undergo transdifferentiation into the intestinal‐type columnar epithelium, transcommittment into the columnar epithelium, or whether the other pathways exist. Reflux of duodenal fluid including bile acids into the stomach may occur when an individual lies down after eating, which could cause the digestive juices to collect in the fornix of the stomach. N‐nitroso‐bile acids are produced with nitrites that are secreted from the salivary glands, and bile acids can drive expression of pro‐inflammatory cytokines via EGFR or the NF‐κB pathway. These steps may contribute significantly to carcinogenesis. John Wiley and Sons Inc. 2019-07-10 2019-06 /pmc/articles/PMC6851828/ /pubmed/31290583 http://dx.doi.org/10.1111/pin.12804 Text en © 2019 The Authors. Pathology International published by the Japanese Society of Pathology and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Review Article Mukaisho, Ken‐ichi Kanai, Shunpei Kushima, Ryoji Nakayama, Takahisa Hattori, Takanori Sugihara, Hiroyuki Barretts's carcinogenesis |
title | Barretts's carcinogenesis |
title_full | Barretts's carcinogenesis |
title_fullStr | Barretts's carcinogenesis |
title_full_unstemmed | Barretts's carcinogenesis |
title_short | Barretts's carcinogenesis |
title_sort | barretts's carcinogenesis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851828/ https://www.ncbi.nlm.nih.gov/pubmed/31290583 http://dx.doi.org/10.1111/pin.12804 |
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