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首页> 外文期刊>World Journal of Gastroenterology >Relationship between expression and distribution of cyclooxygenase-2 and bcl-2 in human gastric adenocarcinoma.
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Relationship between expression and distribution of cyclooxygenase-2 and bcl-2 in human gastric adenocarcinoma.

机译:人胃腺癌中环氧合酶-2和bcl-2表达与分布的关系。

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AIM: To explore expression and distribution features of COX-2 and bcl-2 in human gastric adenocarcinoma tissues and to study its biological significance. METHODS: Totally 36 human gastric carcinoma samples were enrolled in this study (cardiac adenocarcinoma 16 cases, distal gastric adenocarcinoma 20 cases). The expressions of COX-2 and bcl-2 in cancerous tissues and corresponding para-cancerous tissues were investigated by immunohistochemistry using COX-2 polyclonal antibody and bcl-2 monoclonal antibody. The normal gastric mucosa tissues were used as control. RESULTS: The expressions of COX-2 and bcl-2 in gastric carcinoma were significantly higher than that in the para-cancerous tissues (77.8% vs 47.2%, P<0.01, 80.56% vs 58.33%, P<0.05). The expression of COX-2 in cardiac adenocarcinoma was remarkably higher than that in the distal gastric carcinoma (93.8% vs 65.0%, P<0.01). The expression of COX-2 was mainly localized in the cytoplasm of tumor cells and partly in the nucleus. There is a transition of the COX-2 cytoplasmic positivity to nucleic in tumor cells with the increase of gastric carcinoma pathological grade. Interstitial macrophages, fibroblasts and vascular endothelial cells also expressed COX-2. The tissues with higher expression of COX-2 also expressed high level of bcl-2 protein. CONCLUSION: Abnormal expression pattern of COX-2 within the tissues of human gastric cancer is correlated with tumor location and lymph node metastasis. COX-2 may regulate expression of apoptosis suppressor gene (bcl-2) through interaction of tumor cells and stromal cells and play an important role in the generation and development of tumors, which will be of great help in developing new methods for antitumor therapy.
机译:目的:探讨COX-2和bcl-2在人胃腺癌组织中的表达和分布特征,并探讨其生物学意义。方法:本研究共纳入36例人类胃癌样本(心脏腺癌16例,远端胃腺癌20例)。采用免疫组化技术,采用COX-2多克隆抗体和bcl-2单克隆抗体,研究了癌组织及癌旁组织中COX-2和bcl-2的表达。正常胃粘膜组织用作对照。结果:胃癌组织中COX-2和bcl-2的表达显着高于癌旁组织(77.8%vs 47.2%,P <0.01,80.56%vs 58.33%,P <0.05)。 cardiac门腺癌中COX-2的表达明显高于远端胃癌(93.8%vs 65.0%,P <0.01)。 COX-2的表达主要位于肿瘤细胞的细胞质中,部分位于细胞核中。随着胃癌病理学等级的增加,肿瘤细胞中COX-2细胞质阳性向核酸转移。间质巨噬细胞,成纤维细胞和血管内皮细胞也表达COX-2。高表达COX-2的组织也表达高水平的bcl-2蛋白。结论:人胃癌组织中COX-2表达异常与肿瘤的位置和淋巴结转移有关。 COX-2可能通过肿瘤细胞与基质细胞的相互作用来调控凋亡抑制基因(bcl-2)的表达,并在肿瘤的产生和发展中起重要作用,这对开发新的抗肿瘤治疗方法将有很大帮助。

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