Gastroesophageal reflux leads to esophageal cancer in a surgical model with mice

<p>Abstract</p> <p>Background</p> <p>Esophago-gastroduodenal anastomosis with rats mimics the development of human Barrett's esophagus and esophageal adenocarcinoma by introducing mixed reflux of gastric and duodenal contents into the esophagus. However, use of thi...

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Main Authors: Chen Xiaoxin, Yang Chung S, Liu Ba, Hao Jing
Format: Article
Language:English
Published: BMC 2009-07-01
Series:BMC Gastroenterology
Online Access:http://www.biomedcentral.com/1471-230X/9/59
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spelling doaj-48523ffc21474e6388777c4a1fcd45672020-11-25T03:13:34ZengBMCBMC Gastroenterology1471-230X2009-07-01915910.1186/1471-230X-9-59Gastroesophageal reflux leads to esophageal cancer in a surgical model with miceChen XiaoxinYang Chung SLiu BaHao Jing<p>Abstract</p> <p>Background</p> <p>Esophago-gastroduodenal anastomosis with rats mimics the development of human Barrett's esophagus and esophageal adenocarcinoma by introducing mixed reflux of gastric and duodenal contents into the esophagus. However, use of this rat model for mechanistic and chemopreventive studies is limited due to lack of genetically modified rat strains. Therefore, a mouse model of esophageal adenocarcinoma is needed.</p> <p>Methods</p> <p>We performed reflux surgery on wild-type, <it>p53</it><sup><it>A</it>135<it>V </it></sup>transgenic, and <it>INK4a/Arf</it><sup>+/- </sup>mice of A/J strain. Some mice were also treated with omeprazole (1,400 ppm in diet), iron (50 mg/kg/m, <it>i.p</it>.), or gastrectomy plus iron. Mouse esophagi were harvested at 20, 40 or 80 weeks after surgery for histopathological analysis.</p> <p>Results</p> <p>At week 20, we observed metaplasia in wild-type mice (5%, 1/20) and <it>p53</it><sup><it>A</it>135<it>V </it></sup>mice (5.3%, 1/19). At week 40, metaplasia was found in wild-type mice (16.2%, 6/37), <it>p53</it><sup><it>A</it>135<it>V </it></sup>mice (4.8%, 2/42), and wild-type mice also receiving gastrectomy and iron (6.7%, 1/15). Esophageal squamous cell carcinoma developed in <it>INK4a/Arf</it><sup>+/- </sup>mice (7.1%, 1/14), and wild-type mice receiving gastrectomy and iron (21.4%, 3/14). Among 13 wild-type mice which were given iron from week 40 to 80, twelve (92.3%) developed squamous cell carcinoma at week 80. None of these mice developed esophageal adenocarcinoma.</p> <p>Conclusion</p> <p>Surgically induced gastroesophageal reflux produced esophageal squamous cell carcinoma, but not esophageal adenocarcinoma, in mice. Dominant negative <it>p53 </it>mutation, heterozygous loss of <it>INK4a/Arf</it>, antacid treatment, iron supplementation, or gastrectomy failed to promote esophageal adenocarcinoma in these mice. Further studies are needed in order to develop a mouse model of esophageal adenocarcinoma.</p> http://www.biomedcentral.com/1471-230X/9/59
collection DOAJ
language English
format Article
sources DOAJ
author Chen Xiaoxin
Yang Chung S
Liu Ba
Hao Jing
spellingShingle Chen Xiaoxin
Yang Chung S
Liu Ba
Hao Jing
Gastroesophageal reflux leads to esophageal cancer in a surgical model with mice
BMC Gastroenterology
author_facet Chen Xiaoxin
Yang Chung S
Liu Ba
Hao Jing
author_sort Chen Xiaoxin
title Gastroesophageal reflux leads to esophageal cancer in a surgical model with mice
title_short Gastroesophageal reflux leads to esophageal cancer in a surgical model with mice
title_full Gastroesophageal reflux leads to esophageal cancer in a surgical model with mice
title_fullStr Gastroesophageal reflux leads to esophageal cancer in a surgical model with mice
title_full_unstemmed Gastroesophageal reflux leads to esophageal cancer in a surgical model with mice
title_sort gastroesophageal reflux leads to esophageal cancer in a surgical model with mice
publisher BMC
series BMC Gastroenterology
issn 1471-230X
publishDate 2009-07-01
description <p>Abstract</p> <p>Background</p> <p>Esophago-gastroduodenal anastomosis with rats mimics the development of human Barrett's esophagus and esophageal adenocarcinoma by introducing mixed reflux of gastric and duodenal contents into the esophagus. However, use of this rat model for mechanistic and chemopreventive studies is limited due to lack of genetically modified rat strains. Therefore, a mouse model of esophageal adenocarcinoma is needed.</p> <p>Methods</p> <p>We performed reflux surgery on wild-type, <it>p53</it><sup><it>A</it>135<it>V </it></sup>transgenic, and <it>INK4a/Arf</it><sup>+/- </sup>mice of A/J strain. Some mice were also treated with omeprazole (1,400 ppm in diet), iron (50 mg/kg/m, <it>i.p</it>.), or gastrectomy plus iron. Mouse esophagi were harvested at 20, 40 or 80 weeks after surgery for histopathological analysis.</p> <p>Results</p> <p>At week 20, we observed metaplasia in wild-type mice (5%, 1/20) and <it>p53</it><sup><it>A</it>135<it>V </it></sup>mice (5.3%, 1/19). At week 40, metaplasia was found in wild-type mice (16.2%, 6/37), <it>p53</it><sup><it>A</it>135<it>V </it></sup>mice (4.8%, 2/42), and wild-type mice also receiving gastrectomy and iron (6.7%, 1/15). Esophageal squamous cell carcinoma developed in <it>INK4a/Arf</it><sup>+/- </sup>mice (7.1%, 1/14), and wild-type mice receiving gastrectomy and iron (21.4%, 3/14). Among 13 wild-type mice which were given iron from week 40 to 80, twelve (92.3%) developed squamous cell carcinoma at week 80. None of these mice developed esophageal adenocarcinoma.</p> <p>Conclusion</p> <p>Surgically induced gastroesophageal reflux produced esophageal squamous cell carcinoma, but not esophageal adenocarcinoma, in mice. Dominant negative <it>p53 </it>mutation, heterozygous loss of <it>INK4a/Arf</it>, antacid treatment, iron supplementation, or gastrectomy failed to promote esophageal adenocarcinoma in these mice. Further studies are needed in order to develop a mouse model of esophageal adenocarcinoma.</p>
url http://www.biomedcentral.com/1471-230X/9/59
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