van Baal Jantine W P M, Milano Francesca, Rygiel Agnieszka M, Bergman Jacques J G H M, Rosmolen Wilda D, van Deventer Sander J H, Wang Kenneth K, Peppelenbosch Maikel P, Krishnadath Kausilia K
Laboratory of Experimental Internal Medicine, Academic Medical Center, Amsterdam, The Netherlands.
Gastroenterology. 2005 Oct;129(4):1274-81. doi: 10.1053/j.gastro.2005.07.026.
BACKGROUND & AIMS: The metaplastic process in which the normal squamous epithelium of the distal esophagus is replaced by columnar-lined epithelium, known as Barrett's esophagus (BE), is poorly understood. The aim of this study was to define, analyze, and compare transcription profiles of BE, normal cardia epithelium, and squamous epithelium to gain more insight into the process of metaplasia and to identify uniquely expressed genes in these epithelia.
Serial analysis of gene expression was applied for obtaining transcription libraries of biopsy specimens taken from a BE-affected patient with intestinal type of metaplasia and from normal squamous and gastric cardia epithelia. Validation of results by reverse-transcription polymerase chain reaction and immunoblotting was performed using tissues of 20 patients with BE.
More than 120,000 tags were sequenced. Between BE and squamous 776, and between BE and gastric cardia 534 tags were significantly differentially expressed (P < .05, pairwise comparison). In contrast, squamous compared with gastric cardia epithelia showed significant differential expression of 1316 tags. The most up-regulated genes in BE compared with squamous epithelium were trefoil factors, annexin A10, and galectin-4. Each of the epithelia showed a unique cytokeratin expression profile.
This study provides a comparison of the transcriptomes of BE, squamous epithelium, and gastric cardia epithelium. BE proves to be an incompletely differentiated type of epithelium that shows similarities to both normal squamous and gastric cardia epithelia. In addition, several uniquely expressed genes are identified. These results are a major advancement in understanding the process of metaplasia that leads to BE.
远端食管正常鳞状上皮被柱状上皮取代的化生过程,即巴雷特食管(BE),目前了解甚少。本研究旨在定义、分析和比较BE、正常贲门上皮和鳞状上皮的转录谱,以更深入了解化生过程,并鉴定这些上皮中独特表达的基因。
应用基因表达序列分析技术获取取自一名患有肠化生的BE患者的活检标本以及正常鳞状上皮和胃贲门上皮的转录文库。使用20例BE患者的组织通过逆转录聚合酶链反应和免疫印迹对结果进行验证。
测序了超过120,000个标签。BE与鳞状上皮之间有776个标签,BE与胃贲门之间有534个标签存在显著差异表达(P <.05,成对比较)。相比之下,鳞状上皮与胃贲门上皮之间有1316个标签存在显著差异表达。与鳞状上皮相比,BE中上调最明显的基因是三叶因子、膜联蛋白A10和半乳糖凝集素-4。每种上皮都显示出独特的细胞角蛋白表达谱。
本研究对BE、鳞状上皮和胃贲门上皮的转录组进行了比较。BE被证明是一种不完全分化的上皮类型,与正常鳞状上皮和胃贲门上皮都有相似之处。此外,还鉴定了几个独特表达的基因。这些结果是在理解导致BE的化生过程方面的一项重大进展。