Changes in gene expression of gastric mucosa during therapeutic acid inhibition

被引:14
作者
Norsetta, Kristin G. [1 ]
Laegreid, Astrid [1 ]
Kusnierczyk, Waclaw [3 ]
Langaas, Mette
Ylving, Sonja [1 ]
Fossmark, Reidar [1 ,4 ]
Myhre, Simen [1 ]
Falkmer, Sture [2 ]
Waldum, Helge L. [1 ,4 ]
Sandvik, Arne K. [1 ,4 ]
机构
[1] Norwegian Univ Sci & Technol, Dept Canc Res & Mol Med, N-7034 Trondheim, Norway
[2] Norwegian Univ Sci & Technol, Dept Lab Med, Fac Med, N-7034 Trondheim, Norway
[3] Norwegian Univ Sci & Technol, Dept Comp & Informat Sci, Fac Informat Technol Math & Elect Engn, N-7034 Trondheim, Norway
[4] St Olavs Univ Hosp, Trondheim, Norway
关键词
cDNA microarray; esomeprazole; gastrin; proliferation; proton pump inhibitors;
D O I
10.1097/MEG.0b013e3282f5dc19
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Long-term therapy with potent acid inhibitors is a common treatment for gastro-esophageal reflux disease. Administration of proton pump inhibitors (PPIs) causes profound and continuous hypochlorhydria by inhibition of the proton pump in gastric parietal cells. Long-term hypergastrinaemia increases mucosal thickness and enterochromaffin-like cell density in oxyntic mucosa. Objective The aim of this study was to see whether this very common clinical intervention induces significant changes in the gastric mucosal gene expression pattern. Methods Seven patients suffering from gastroesophageal reflux disease were included in this study. Endoscopic biopsies were taken from the corpus mucosa before and toward the end of a 3-month treatment with the PPI esomeprazole. Results Microarray analysis identified 186 differentially expressed genes. A high proportion of genes with changed gene expression levels during PPI treatment are involved in proliferation, apoptosis, and stress response. Conclusion This study identified many genes that were not previously known to be affected by inhibition of gastric acid secretion. Further characterization of the functional roles of genes whose expression is modulated by potent acid inhibition may give new insight into the biological responses to potent acid inhibition, including the mucosal response to the moderately increased gastrin levels encountered in clinical practice.
引用
收藏
页码:613 / 623
页数:11
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