A Mouse Model for Barrett’s Esophagus: Surgery and Histology

A. Taddei, T. Lottini, M. Fazi, M. Ringressi, E. Lastraioli, P. Bechi, A. Arcangeli
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引用次数: 2

Abstract

Purpose: Barrett’s esophagus (BE) is the sole precursor lesion of esophageal adenocarcinoma (EA) identified so far. The progression towards EA is estimated to affect 2 to 10% of BE patients, hence endoscopic surveillance of at-risk subjects is mandatory. Surveillance endoscopic procedures imply high cost, discomfort and risks for the patient, as well as the non-infrequent missing of small, focal lesions signaling progression to EA. Hence, it is important to search for new potential markers to better identify BE patients at risk of EA progression. The aim of this study was to produce a mouse model of BE, suitable for further molecular and genetic analyses. Methods: Forty-four CD1 mice were operated upon by means of an esophago-jejunal anastomosis. Five CD1 mice underwent a sham operation. The animals were sacrificed 10 months later and histological analysis was performed with Hematoxylin & Eosin and Alcian Blue staining. Results: The overall postoperative mortality rate was 11%. Of the 39 operated animals 14% developed histologically detectable intestinal metaplasia in the lower esophagus. No histologically detectable lesions were shown in the sham group. Conclusions: The mice model we propose could be applied because of its technical feasibility and acceptable mortality and can be used in transgenic mice too, in order to better understand molecular progression from BE to esophageal adenocarcinoma.
小鼠Barrett食管模型:手术与组织学
目的:Barrett食管(BE)是目前发现的唯一一种食管腺癌(EA)的前体病变。据估计,2 - 10%的BE患者会发展为EA,因此必须对有风险的受试者进行内窥镜监测。内窥镜检查对患者来说意味着高昂的费用、不适和风险,而且通常会丢失指示EA进展的小的局灶性病变。因此,寻找新的潜在标记物来更好地识别有EA进展风险的BE患者是很重要的。本研究的目的是建立一种适合进一步分子和遗传分析的BE小鼠模型。方法:采用食道-空肠吻合术对44只CD1小鼠进行手术。5只CD1小鼠接受了假手术。10个月后处死动物,采用苏木精&伊红染色和阿利新蓝染色进行组织学分析。结果:术后总死亡率为11%。在39只手术动物中,14%在食管下部发生组织学可检测的肠化生。假手术组未见组织学上可检测到的病变。结论:所建立的小鼠模型具有技术可行性和可接受的死亡率,并可用于转基因小鼠,以更好地了解从be到食管癌的分子进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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