Morrice L M, McIntosh L C, Thomson A W
Department of Pathology, University of Aberdeen, Scotland, UK.
Oncology. 1987;44(6):378-82. doi: 10.1159/000226514.
The direct procoagulant activity (PCA) of murine tumour cells was found to be more than three orders of magnitude greater than an equivalent concentration of either resident or Corynebacterium parvum-elicited, exudate peritoneal cells. Similarly, a soluble PCA was detected in the extracellular culture medium of only the tumour cells. Studies on the procoagulant nature of the serum and ascitic fluid of tumour-bearing animals suggested that the ascitic fluid may contain a unique PCA factor(s). This activity could not, however, be resolved from inherent procoagulant factors, either by gel filtration or ammonium sulphate fractionation, and a more specific assay for, say, a single enzymic reaction in the coagulation cascade would be required to identify the tumour-associated activity.
已发现鼠肿瘤细胞的直接促凝血活性(PCA)比同等浓度的驻留腹膜细胞或微小棒状杆菌诱导的渗出性腹膜细胞高出三个数量级以上。同样,仅在肿瘤细胞的细胞外培养基中检测到可溶性PCA。对荷瘤动物血清和腹水促凝血性质的研究表明,腹水可能含有独特的PCA因子。然而,通过凝胶过滤或硫酸铵分级分离,这种活性无法与内在的促凝血因子区分开来,需要一种更特异的检测方法,比如针对凝血级联反应中单个酶促反应的检测方法,来鉴定肿瘤相关活性。