Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3841289 | Translational Research | 2008 | 7 Pages |
Abstract
Although the pathogenesis and treatment of erosive esophagitis (EE) is well recognized, little is known about the cellular and molecular mechanisms of mucosal healing in EE patients. In this pilot study, we enrolled typical EE patients to evaluate what kinds of growth factors and their receptors were activated in their injured esophageal mucosa. Forty endoscopically proved EE patients were consecutively enrolled. Messenger RNA expressions, which includes keratinocyte growth factor (KGF) and its receptor (KGFR), epidermal growth factor (EGF) and its receptor (EGFR), hepatocyte growth factor (HGF) and its receptor (HGFR), basic fibroblast growth factor (bFGF), vascular endothelial growth factor (VEGF), and cyclooxygenase (COX)-1 and COX-2, were measured using real-time polymerase chain reaction (PCR). Data were compared between the injured EE mucosa and their normal esophageal mucosa above EE. The mRNA expressions of HGF, HGFR, EGF, VEGF, and COX-2, but not EGFR, KGF, KGFR, bFGF, and COX-1, were significantly increased in the injured mucosa of EE patients compared with those of normal mucosa (P < 0.05). The study found that HGF, HGFR, EGF, VEGF, and, COX-2 are activated in the injured mucosa of EE patients; their activation might be involved in mucosal repair and ulcer healing of EE.
Keywords
NSAIDSEGFREGFHGFRKGF receptorCOXKGFRHGF receptorKGFbFGFHGFPPIGERDERKcyclooxygenasegastroesophageal reflux diseasestandard error of the meanNonsteroidal anti-inflammatory drugsextracellular signal regulated kinaseepidermal growth factorHepatocyte growth factorKeratinocyte growth factorVascular endothelial growth factorVascular Endothelial Growth Factor (VEGF)basic fibroblast growth factorSEMErosive esophagitisProton pump inhibitorpolymerase chain reactionPCREGF receptor
Related Topics
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Medicine and Dentistry (General)
Authors
Jiing-Chyuan Luo, Hsiao-Yi Lin, Ching-Liang Lu, Tseng-Shing Chen, Han-Chieh Lin, Chung-Pin Li, Wei-Chih Liao, Full-Young Chang, Shou-Dong Lee,