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首页> 外文期刊>The Journal of laboratory and clinical medicine >Relationships among tumor burden, tumor size, and the changing concentrations of fibrin degradation products and fibrinolytic factors in the pleural effusions of rabbits with VX2 lung tumors.
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Relationships among tumor burden, tumor size, and the changing concentrations of fibrin degradation products and fibrinolytic factors in the pleural effusions of rabbits with VX2 lung tumors.

机译:VX2肺肿瘤兔胸腔积液中肿瘤负荷,肿瘤大小以及纤维蛋白降解产物和纤溶因子浓度变化之间的关系。

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The VX2 tumor is derived from a papilloma virus-induced rabbit epithelial cell line. If VX2 tumor cells (trapped in a plasma clot) are introduced intravenously into NZW rabbits, the cells lodge in the lung capillary bed and produce tumors. Independently of the tumor burden (ie, the total tumor weight per rabbit), approximately 15% of rabbits with VX2 lung tumors accumulate an effusion in the interpleural space and this pleural effusion contains products of hemostasis. We hypothesized that these products were of intra-tumoral origin and that they changed in concentration as tumor burden increased. Interrelationships among lung-, tumor-weights, and pleural effusion volumes, and the concentrations of fibrinolytic factors, their catabolic products, and other proteins of pleural effusions were measured in rabbits with a wide range of tumor burdens. Positive correlations between tumor burden and total lung weight and between pleural effusion volume and net lung weight suggested that interstitial fluid from the stroma of tumors passed directly into the extravascular space of the lung(s) and into the interpleural space(s). Analyses of pleural effusions indicated that plasminogen-, alpha(2)-antiplasmin-, and plasminogen activator inhibitor-1-related proteins, urokinase-like- and tissue-plasminogen activator activities, and vascular endothelial growth factor increased in concentration up to a tumor burden of approximately 20-25 g. Plasmin activity and intact fibrinogen were absent. The concentration of fibrin(ogen) degradation products did not change significantly up to a tumor burden of approximately 25 g but increased substantially as tumor burdens exceeded 25 g. In conclusion, interstitial fluid from tumors enters the extravascular space of the host and may accumulate with fluid from non-tumor sources as a pleural effusion. The concentrations of fibrinolytic factors and their products in pleural effusions reflect the tumor burden of the rabbit. Conceivably, the components of a malignant effusion contain much information about the extent of tumor growth.
机译:VX2肿瘤源自乳头瘤病毒诱导的兔上皮细胞系。如果将VX2肿瘤细胞(困在血浆凝块中)静脉内导入NZW家兔,则这些细胞会滞留在肺毛细血管床中并产生肿瘤。与肿瘤负荷(即每只兔子的总肿瘤重量)无关,大约15%的具有VX2肺肿瘤的兔子在胸膜间隙积聚积液,并且该胸膜积积有止血产物。我们假设这些产物是肿瘤内起源的,并且它们的浓度随着肿瘤负荷的增加而变化。在患有多种肿瘤负担的兔子中,测量了肺重量,肿瘤重量和胸腔积液之间的相互关系,以及纤溶因子,其分解代谢产物和胸腔积液其他蛋白的浓度。肿瘤负荷和总肺重量之间以及胸腔积液量和净肺重量之间的正相关性表明,来自肿瘤基质的组织液直接进入肺的血管外腔和胸膜间腔。胸腔积液的分析表明,纤溶酶原,α(2)-抗纤溶酶和纤溶酶原激活物抑制剂-1相关蛋白,尿激酶样和组织纤溶酶原激活物活性以及血管内皮生长因子的浓度一直升高到肿瘤为止负担约20-25克。缺乏纤溶酶活性和完整的纤维蛋白原。直至约25g的肿瘤负荷,血纤蛋白(基因)降解产物的浓度没有显着变化,但是随着肿瘤负荷超过25g而显着增加。总之,来自肿瘤的间质液进入宿主的血管外空间,并可能由于胸腔积液而与来自非肿瘤源的液积聚。胸腔积液中纤维蛋白溶解因子及其产物的浓度反映了兔子的肿瘤负担。可以想象,恶性积液的成分包含许多有关肿瘤生长程度的信息。

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