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Correlation between expression of cyclooxygenase-2 and the presence of inflammatory cells in human primary hepatocellular carcinoma: possible role in tumor promotion and angiogenesis.

机译:人类原发性肝细胞癌中环氧合酶2的表达与炎症细胞的存在之间的相关性:在肿瘤促进和血管生成中的可能作用。

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摘要

im: To investigate the association of cyclooxygenase-2 (COX-2) expression with angiogenesis and the number and type of inflammatory cells (macrophages/Kupffer cells; mast cells) within primary hepatocellular carcinoma (HCC) tissues and adjacent non-tumorous (NT) tissues. Methods: Immunohistochemistry for COX-2, CD34, CD68 and mast cell tryptase (MCT) was performed on 14 well-characterized series of liver-cirrhosis-associated HCC patients. COX-2 expression and the number of inflammatory cells in tumor lesions and surrounding liver tissues of each specimen were compared. Moreover, COX-2, CD34 staining and the number of inflammatory cells in areas with different histological degrees within each tumor sample were comparatively analyzed. Results: The percentage of COX-2 positive cells was significantly higher in NT tissues than in tumors. COX-2 expression was higher in well-differentiated HCC than in poorly-differentiated tissues. Few mast cells were observed within the tumor mass, whereas a higher number was observed in the surrounding tissue, especially in peri-portal spaces of NT tissues. Abundant macrophages/Kupffer cells were observed in NT tissues, whereas the number of cells was significantly lower in the tumor mass. However, a higher cell number was observed in the well-differentiated tumor and progressively decreased in relation to the differentiation grade. Within the tumor, a positive correlation was found between COX-2 expression and the number of macrophages/Kupffer cells and mast cells. Moreover, there was a positive correlation between CD34 and COX-2 expression in tumor tissues. Comparison between well- and poorly-differentiated HCC showed that the number of CD34-positive cells decreased with dedifferentiation. However, COX-2 was the only independent variable showing a positive correlation with CD34 in a multivariate analysis. Conclusion: The presence of inflammatory cells and COX-2 expression in liver tumor suggests a possible relationship with tumor angiogenesis. COX-2 expressing cells and the number of macrophages/Kupffer cells and mast cells decrease with progression of the disease
机译:即时消息:研究环氧合酶2(COX-2)表达与血管生成以及原发性肝细胞癌(HCC)组织和邻近非肿瘤性(NT)中炎性细胞(巨噬细胞/库普弗细胞;肥大细胞)的数量和类型之间的关系)组织。方法:对14例特征明确的肝硬化相关的HCC患者进行了COX-2,CD34,CD68和肥大细胞类胰蛋白酶(MCT)的免疫组织化学分析。比较每个样品的肿瘤病变和周围肝组织中COX-2的表达和炎性细胞的数量。此外,比较了每个肿瘤样品中具有不同组织学程度的区域的COX-2,CD34染色和炎性细胞数量。结果:NT组织中COX-2阳性细胞的百分比明显高于肿瘤。高分化HCC中的COX-2表达高于低分化组织中的COX-2表达。在肿瘤块内几乎没有观察到肥大细胞,而在周围组织中观察到了更多的肥大细胞,特别是在NT组织的近门间隙。在NT组织中观察到大量的巨噬细胞/库普弗细胞,而肿瘤块中的细胞数量则明显减少。然而,在分化良好的肿瘤中观察到更高的细胞数,并且相对于分化等级逐渐降低。在肿瘤内,发现COX-2表达与巨噬细胞/库普弗细胞和肥大细胞之间呈正相关。此外,在肿瘤组织中CD34和COX-2表达之间存在正相关。高分化和低分化肝癌之间的比较表明,CD34阳性细胞的数量随着去分化而减少。然而,在多变量分析中,COX-2是唯一显示与CD34正相关的独立变量。结论:肝肿瘤中炎性细胞的存在和COX-2的表达提示可能与肿瘤血管生成有关。随着疾病的发展,表达COX-2的细胞以及巨噬细胞/库普弗细胞和肥大细胞的数量减少

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