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Association of cyclooxygenase-2 expression with Hp-cagA infection in gastric cancer

机译:环氧合酶-2表达与胃癌Hp-cagA感染的关系

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AIM: To observe the expression of cyclooxygenase-2 (COX-2) and to investigate the association between COX-2 expression and infection with cytotoxic-associated gene A (cagA) positive strain Helicobacter pylori (Hp) in human gastric cancer, and subsequently to provide fresh ideas for the early prevention of gastric cancer. METHODS: 32 Specimens of gastric cancer and corresponding adjacent normal gastric mucosa were obtained from patients who had undergone surgical operations of gastric cancer. All the samples including 1 case of stomach malignant lymphoma and 31 cases of gastric adenocarcinoma were confirmed by pathology diagnosis. The expression of COX-2 in 32 specimens of gastric cancer and corresponding adjacent normal gastric mucosa was quantitatively determined and analyzed with Flow Cytometry, and the levels of COX-2 protein were compared between specimens with cagA~+ Hp infection and those without cagA~+ Hp infection. The cagA gene in 32 specimens of gastric cancer was detected by polymerase chain reaction (PCR) method. RESULTS: Twenty-seven of 32 (84%) specimens of gastric cancer showed over-expression of COX-2, compared with the adjacent normal gastric mucosa. cagA~+ gene were detected from 19 specimens of gastric cancer, but not from the other 13 specimens. The levels of COX-2 protein in 19 specimens of gastric cancer with cagA~+ Hp infection (the number of positive cells was 73.82+-18.2) were significantly higher than those in the 13 specimens without cagA~+ Hp infection (the number of positive cells was 35.92+-22.1). CONCLUSION: COX-2 is overexpressed in gastric cancer and cagA~+ Hp infection could up-regulate the expression of COX-2 in gastric cancer in human. There may also exist another way or channel to regulate the expression of COX-2 in gastric cancer in addition to cagA~+ Hp infection. Therefore, applying COX-2 selective inhibitors could be an effective and promising way to prevent gastric cancer.
机译:目的:观察环氧合酶-2(COX-2)的表达,并研究COX-2表达与细胞毒相关基因A(cagA)阳性菌株幽门螺杆菌(Hp)感染在人类胃癌中的关系,并随后对其进行研究。为早期预防胃癌提供新的思路。方法:从接受过胃癌手术的患者中获得32份胃癌及相应的邻近正常胃黏膜标本。经病理诊断,全部标本包括胃恶性淋巴瘤1例和胃腺癌31例。用流式细胞仪定量测定和分析32例胃癌及相应的邻近正常胃黏膜标本中COX-2的表达,并比较cagA〜+ Hp感染和未感染cagA〜的标本中COX-2的表达水平。 + Hp感染。用聚合酶链反应(PCR)法检测32例胃癌标本中的cagA基因。结果:与相邻的正常胃黏膜相比,32例胃癌标本中有27例显示COX-2过表达。从19例胃癌标本中检测到cagA〜+基因,而其他13例标本中未检测到。 19例cagA〜+ Hp感染的胃癌标本中COX-2蛋白的水平(阳性细胞数为73.82 + -18.2)显着高于13例无cagA〜+ Hp感染的胃癌标本中的COX-2蛋白水平。阳性细胞为35.92 + -22.1)。结论:COX-2在胃癌中高表达,cagA〜+ Hp感染可上调人胃癌中COX-2的表达。除cagA〜+ Hp感染外,可能还存在另一种途径或途径来调节COX-2在胃癌中的表达。因此,使用COX-2选择性抑制剂可能是预防胃癌的有效途径。

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