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1.
Chinese Journal of Oncology ; (12): 120-122, 2006.
Article Dans Chinois | WPRIM | ID: wpr-308405

Résumé

<p><b>OBJECTIVE</b>To study the expression and significance of interleukin-8 (IL-8), cyclooxygenase-2 (COX-2) and trefoil family factor 1 (TFF1) in the remnant stomach mucosa.</p><p><b>METHODS</b>Patients after gastrectomy were examined by upper gastrointestinal endoscopy. Biopsy specimens were obtained from stoma and the greater curvature of the upper corpus to be assessed for Hp (by H.E. and Giemsa staining) and conduct real-time semi-quantitative PCR. mRNA was extracted from the biopsy specimens to determine the IL-8, COX-2 and TFF1 gene mRNA levels by real-time PCR method.</p><p><b>RESULTS</b>In the stoma, COX-2 level in Hp-positive patients was significantly higher than that in Hp-negative patients, but the difference of IL-8 levels between them was not significant. In the corpus, IL-8 and COX-2 levels in Hp-positive patients were significantly higher than those in Hp-negative patients. In Hp-negative patients, IL-8 and COX-2 levels in the stoma were significantly higher in B II anastomosis than in B I anastomosis cases; COX-2 level in the stoma was significantly higher in B II anastomosis than in B I anastomosis cases, but the difference of IL-8 levels between them was not significant. TFF1 level in the remnant stomach mucosa showed no significant difference between Hp-positive and Hp-negative patients.</p><p><b>CONCLUSION</b>Hp infection and bile reflux are important risk factors for the secondary stomach carcinogenesis. Expression of IL-8 and COX-2 in the remnant stomach mucosa is related to the risk of secondary stomach carcinogenesis. The relationship between the TFF1 expression and secondary stomach carcinogenesis in the remnant stomach mucosa is still unclear and should further be studied.</p>


Sujets)
Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Femelle , Humains , Mâle , Adulte d'âge moyen , Cyclooxygenase 2 , Génétique , Gastrectomie , Muqueuse gastrique , Métabolisme , Moignon gastrique , Infections à Helicobacter , Métabolisme , Helicobacter pylori , Interleukine-8 , Génétique , ARN messager , Génétique , Facteurs de risque , Tumeurs de l'estomac , Métabolisme , Microbiologie , Chirurgie générale , Facteur en trèfle-1 , Protéines suppresseurs de tumeurs , Génétique
2.
Chinese Journal of Surgery ; (12): 166-168, 2005.
Article Dans Chinois | WPRIM | ID: wpr-345023

Résumé

<p><b>OBJECTIVE</b>To study the expressions and the significance of interleukin-8 (IL-8) and cyclooxygenase-2 (COX-2) in the remnant stomach.</p><p><b>METHODS</b>Fifty-eight patients with gastrectomy were examined by upper gastrointestinal endoscopy. Two biopsy specimens were obtained from the stoma and the upper corpus gastric mucosa in the remnant stomach. mRNA was extracted from biopsy specimens to measure the IL-8 and COX-2 gene mRNA levels by real-time PCR method.</p><p><b>RESULTS</b>IL-8 and COX-2 levels were higher in stoma than in corpus, IL-8 levels in BI anastomosis were significantly higher in stoma than in corpus (P< 0.05). In Hp-negative patients, IL-8 and COX-2 levels in stoma were significantly higher in BII anastomosis than in BI anastomosis (P < 0.05). In Hp-positive patients, IL-8 and COX-2 levels in stoma showed no significant differences between BII anastomosis and BI anastomosis. In corpus, IL-8 and COX-2 levels in Hp-positive patients were significantly higher than those in Hp-negative patients, (P < 0.05), including in BI anastomosis and in BII anastomosis.</p><p><b>CONCLUSIONS</b>The risk of the secondary stomach carcinogenesis in stoma after distal gastrectomy is higher than that in corpus; The types of anastomosis may influence the risk for the secondary stomach carcinogenesis in the remnant stomach mucosa.</p>


Sujets)
Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Femelle , Humains , Mâle , Adulte d'âge moyen , Muqueuse gastrique , Métabolisme , Microbiologie , Moignon gastrique , Chirurgie générale , Gastroentérostomie , Méthodes , Infections à Helicobacter , Helicobacter pylori , Interleukine-8 , Génétique , Prostaglandin-endoperoxide synthases , Génétique , ARN messager , Tumeurs de l'estomac
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