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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Interaction of Cyclooxygenase-2 with Helicobacter pylori Induces Gastric Chronic Nonresolving Inflammation and the Formation of Syndrome of Internal Block of Static Blood in Helicobacter pylori-Related Gastric Diseases
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Interaction of Cyclooxygenase-2 with Helicobacter pylori Induces Gastric Chronic Nonresolving Inflammation and the Formation of Syndrome of Internal Block of Static Blood in Helicobacter pylori-Related Gastric Diseases

机译:环氧氧酶-2与幽门螺杆菌的相互作用诱导胃慢性非溶解炎症和幽门螺杆菌相关胃病中静血血液内块综合征的形成

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摘要

Cyclooxygenase-2 (COX-2) is an inducible enzyme stimulated by various inflammatory factors (IFs). Chronic gastritis is a classic model of “inflammation-cancer transformation” and Helicobacter pylori-related gastric diseases (HPGD) are specific ones of this model. Traditional Chinese Medicine (TCM) syndromes could play a predictive role in gastric histopathological evolution. To search for early warning evidence about “inflammation-cancer transformation,” this study is about to explore interaction of COX-2 with Helicobacter pylori (Hp) in HPGD with different TCM syndromes. All included subjects underwent endoscopy and biopsy. Hp infection was detected by rapid urease test and methylene blue staining. Histopathological characteristics and COX-2 expression in gastric mucosa (GM) were, respectively, observed by hematoxylin-eosin and Elivision? plus. SPSS 18.0 and Stata 11.0 statistical software packages were used for statistical analysis. Results of immunohistochemical staining in this study showed COX-2 expression in Hp-positive patients was stronger than that in Hp-negative ones. Spearman’ analysis indicated that degrees of both Hp infection and COX-2 expression were positively correlated with those of gastric inflammation and inflammatory activity. Compared with the relative normal group, both severe dysplasia group and gastric carcinoma group had more severe Hp infection and COX-2 expression. Compared with the nonsyndrome, syndrome of internal block of static blood (IBSB) had higher scores in semiquantitative analysis of COX-2 protein expression among TCM groups. Moreover, multivariate logistics regression analysis suggested that patients with Hp infection could increase the risk of IBSB. These results indicated that COX-2 interacting with Hp could play an important role in transforming gastric chronic nonresolving inflammation into carcinoma in subjects with HPGD, as well as inducing the formation of IBSB. HPGD together with IBSB could be an early warning evidence for GM with histopathological evolution from benign to malignant.
机译:环氧氧酶-2(COX-2)是由各种炎症因子(IFS)刺激的诱导酶。慢性胃炎是“炎症 - 癌症转化”和幽门螺杆菌相关胃病(HPGD)的经典模型是该模型的特异性。中药(TCM)综合征可以在胃组织病理学进化中发挥预测作用。为了寻找关于“炎症 - 癌症转化”的预警证据,本研究即将探讨COX-2与幽门螺杆菌(HP)在HPGD中的相互作用,具有不同的TCM综合征。所有包括受试者接受内窥镜检查和活组织检查。通过快速脲酶试验和亚甲基蓝染色来检测HP感染。分别观察胃粘膜(GM)中的组织病理学特征和COX-2表达,观察到苏木精 - 曙红和Elivirision?加。 SPSS 18.0和Stata 11.0统计软件包用于统计分析。本研究中免疫组织化学染色的结果表明,HP阳性患者中的COX-2表达比HP阴性患者更强。 Spearman的分析表明,HP感染和COX-2表达的程度与胃炎症和炎症活性正相关。与相对正常组相比,严重的发育不良组和胃癌基团都具有更严重的HP感染和COX-2表达。与非同学相比,静态血液块(IBSB)的综合征在TCM组中COX-2蛋白表达的半定量分析中具有更高的分数。此外,多变量物流回归分析表明HP感染的患者可能会增加IBSB的风险。这些结果表明,与HP的COX-2相互作用可以在将胃慢性非溶解炎症转化为HPGD的受试者中的癌症中发挥重要作用,以及诱导IBSB的形成。 HPGD与IBSB一起可能是GM的预警证据,具有从良性到恶性的组织病理学演变。

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