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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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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