Dvorak H F, Harvey V S, McDonagh J
Cancer Res. 1984 Aug;44(8):3348-54.
Radiolabeled guinea pig fibrinogen (GPF) was used to measure fibrinogen influx and fibrin accumulation in line 1 and line 10 hepato- (bile duct) carcinomas growing in the s.c. space of syngeneic strain 2 guinea pigs over the course of 7 days following transplant, an interval of growth uncomplicated by immunological tumor rejection or by significant tumor necrosis. Earlier immunofluorescence studies revealed fibrin deposits in both tumors with line 1 much greater than line 10. In accord with these data, GPF accumulated in both tumors in amounts that matched or exceeded plasma fibrinogen levels. Line 1 tumor GPF content was 4-fold greater than that of line 10 tumors and 11- to 33-fold that of normal s.c. tissue. The composition of tumor fibrinogen-fibrin was investigated by aqueous and urea extraction. The fraction of total accumulated GPF that was urea insoluble, and therefore presumably cross-linked fibrin, was constant over time but strikingly different for line 1 (65%) and line 10 (48%) tumors, as compared with control s.c. tissue (18%). By 7 days, line 1 tumors (mean weight, 0.77 g) contained nearly 2 mg of fibrinogen-fibrin, and line 10 tumors (mean weight, 0.62 g) contained nearly 0.5 mg. Influx of GPF and initial clotting were constant over time and equivalent for the two tumors. Hence, the large differences in GPF accumulation observed between these tumors apparently reflect differences in fibrinolysis, not in fibrinogen influx or coagulation. The data presented indicate substantial traffic of plasma fibrinogen into and out of both tumors, as compared with control tissues, equivalent to nearly 10 and 7 ml of plasma over 7 days of growth for line 1 and line 10 tumors, respectively; comparable values for normal s.c. tissues were 1.0 to 1.4 ml plasma fibrinogen. Even in line 1 tumors with their abundant fibrin gel, only 6.3% of GPF entering tumors over 7 days was retained, as compared with 2% for line 10 tumors and approximately 1% for control tissue.
放射性标记的豚鼠纤维蛋白原(GPF)用于测量同基因2系豚鼠皮下生长的1号线和10号线肝癌(胆管癌)在移植后7天内纤维蛋白原的流入和纤维蛋白的积累情况,此生长间隔未出现免疫性肿瘤排斥或显著肿瘤坏死等复杂情况。早期免疫荧光研究显示,两种肿瘤中均有纤维蛋白沉积,1号线肿瘤中的纤维蛋白沉积量远多于10号线肿瘤。与这些数据一致,GPF在两种肿瘤中的积累量与血浆纤维蛋白原水平相当或超过血浆纤维蛋白原水平。1号线肿瘤的GPF含量比10号线肿瘤高4倍,是正常皮下组织的11至33倍。通过水提取和尿素提取研究了肿瘤纤维蛋白原 - 纤维蛋白的组成。尿素不溶性的、因此可能是交联纤维蛋白的累积GPF总量的比例随时间恒定,但与对照皮下组织(18%)相比,1号线肿瘤(65%)和10号线肿瘤(48%)的该比例显著不同。到第7天,1号线肿瘤(平均重量0.77 g)含有近2 mg纤维蛋白原 - 纤维蛋白,10号线肿瘤(平均重量0.62 g)含有近0.5 mg。GPF的流入和初始凝血随时间恒定,两种肿瘤情况相当。因此,这些肿瘤之间观察到的GPF积累的巨大差异显然反映了纤维蛋白溶解的差异,而非纤维蛋白原流入或凝血的差异。所呈现的数据表明,与对照组织相比,血浆纤维蛋白原大量进出两种肿瘤,1号线和10号线肿瘤在生长7天内分别相当于近10 ml和7 ml血浆;正常皮下组织的相应值为1.0至1.4 ml血浆纤维蛋白原。即使在富含纤维蛋白凝胶的1号线肿瘤中,7天内进入肿瘤的GPF仅有6.3%被保留,而10号线肿瘤为2%,对照组织约为1%。