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Dickkopf Homologs in Squamous Mucosa of Esophagitis Patients Are Overexpressed Compared with Barrett's Patients and Healthy Controls

医学 胃肠病学 下调和上调 嗜酸性食管炎 内科学 活检 病理 基因表达 微阵列分析技术 微阵列 基因 疾病 生物 生物化学
作者
Irshad Ali,Parvaneh Rafiee,Walter J. Hogan,Howard J. Jacob,Richard Komorowski,George B. Haasler,Reza Shaker
出处
期刊:The American Journal of Gastroenterology [American College of Gastroenterology]
卷期号:101 (7): 1437-1448 被引量:21
标识
DOI:10.1111/j.1572-0241.2006.00584.x
摘要

OBJECTIVES Esophageal mucosal response to acid exposure varies from minimal changes to erosions/ulcerations and Barrett's metaplasia. While differences in acid contact time have been suggested, the reason for these different responses is not completely understood. The aim of this study was to identify and compare gene expression differences between normal distal and proximal squamous esophageal mucosa (SM) in esophagitis patients with that of healthy controls and Barrett's patients. METHODS Gene microarray was performed on laser-capture microdissected epithelial cells isolated from biopsy specimens followed by real-time PCR. The effect of acidic pH (pH 4.5) on Dickkopf Homolog 1 (Dkk-1) expression in the human esophageal epithelial cell line (Het-1A) was determined. RESULTS Gene microarray analysis demonstrated that the upregulation of five genes in the distal compared with the proximal SM in esophagitis patients was greater than the healthy controls and Barrett's patients. Overexpression of Dkk-1 and Dkk-4 was further confirmed by real-time PCR. Dkk-1 and Dkk-4 mRNA levels in the distal SM of the esophagitis patients were 7.0- and 3.1-fold higher, respectively, than in the distal SM of the Barrett's patients and 4.1- and 4.1-fold higher than in healthy controls, respectively. Dkk-1 protein expression in the distal esophagitis SM was also higher than the Barrett's patients and healthy controls. Acidic pH exposure of Het-1A cells resulted in Dkk-1 upregulation at the level of both mRNA and protein. CONCLUSIONS Dkk-1 and Dkk-4 may potentially be involved in the development of different injuries in response to pathological gastroesophageal acid reflux.
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