吲哚美辛
基因表达
逆转录聚合酶链式反应
信使核糖核酸
粘蛋白
医学
细胞培养
分子生物学
癌症研究
生物
基因
生物化学
病理
体外
前列腺素内过氧化物合酶
遗传学
酶抑制剂
作者
Ayako Koitabashi,Tadahito Shimada,Yasutoshi Fujii,Takashi Hashimoto,K. Hosaka,Kaoru Tabei,Takashi Namatame,Masashi Yoneda,H. Hiraishi,Akira Terano
标识
DOI:10.1111/j.1365-2036.2004.01991.x
摘要
Trefoil factor family peptides are expressed in gastrointestinal epithelial cells and play a critical role in maintaining mucosal integrity. Although non-steroidal anti-inflammatory drugs (NSAIDs) are important causative agents of gastric mucosal lesions, few data are available about the effect of NSAIDs on trefoil family peptides in gastric mucosa.To examine whether indometacin, a widely used NSAID, affects trefoil factor family expression in gastric epithelial cells.MKN45, a cell line derived from human gastric cancer, was used. TFF1, TFF2, and TFF3 mRNA expression was assessed by real-time quantitative reverse transcription-polymerase chain reaction (RT-PCR). TFF2 gene transcription was also examined by luciferase reporter gene assay.Relative expression level of TFF1, TFF2, TFF3 mRNA was 616: 12: 1 in unstimulated MKN45 cells. Although indometacin (1-250 micro mol/L) had no significant effect on the expression of TFF1 and TFF3 mRNA, it up-regulated TFF2 mRNA expression in a dose- and time-dependent manner. Luciferase reporter gene assay confirmed the up-regulation of TFF2 gene transcription by indometacin. Indometacin-induced up-regulation of TFF2 expression was not antagonized by externally applied prostaglandin E2.These results suggest that indometacin up-regulates gastric epithelial cell TFF2 expression through a COX-independent mechanism. Since TFF peptides play an important role in gastric mucosal protection, indometacin-induced TFF2 may reduce the degree of gastric mucosal damage induced by indometacin.
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