Schultek T, Tode B, Wood W G
J Clin Chem Clin Biochem. 1986 Mar;24(3):179-84.
Serum caeruloplasmin levels were measured in women with ovarian, collum and corpus carcinomata using three different assay methods. The enzyme assay gave a median value of 0.26 g/l, the SPALT (solid phase antigen luminescence technique) a median value of 0.78 g/l and the ILMA (immunoluminometric assay) a median of 0.44 g/l. A group of blood donors, taken as the reference group, had a median value of 0.29 g/l in the SPALT assay, which was significantly lower than in the tumour group measured by this method. The ILMA and enzymatic assay values were not significantly different from those measured in the reference group. The differences in the SPALT method can be ascribed to the possibility that this assay measures not only "intact" caeruloplasmin but also paraneoplastic substances with "caeruloplasmin-like immunoactivity". The median of the concentration of tissue polypeptide antigen (TPA) was significantly different from those measured in the reference group. The concentrations of carcinoembryonic antigen (CEA) were not different from the reference group.
采用三种不同的检测方法对患有卵巢癌、宫颈癌和子宫内膜癌的女性血清铜蓝蛋白水平进行了测量。酶法检测得到的中位数为0.26 g/l,固相抗原发光技术(SPALT)得到的中位数为0.78 g/l,免疫发光法(ILMA)得到的中位数为0.44 g/l。作为参照组的一组献血者在SPALT检测中的中位数为0.29 g/l,显著低于用该方法检测的肿瘤组。ILMA和酶法检测值与参照组测得的值无显著差异。SPALT方法中的差异可能归因于该检测不仅能测量“完整的”铜蓝蛋白,还能测量具有“铜蓝蛋白样免疫活性”的副肿瘤物质。组织多肽抗原(TPA)浓度的中位数与参照组测得的有显著差异。癌胚抗原(CEA)浓度与参照组无差异。