Müller T, Bowen M, de Mello J, Pidcock N B, Cooper E H
Eur J Cancer Clin Oncol. 1982 Apr;18(4):327-32. doi: 10.1016/0277-5379(82)90001-3.
The development of a new enzyme-linked immunoassay for pregnancy-associated alpha-2 glycoprotein (alpha 2-PAG) has provided an opportunity to reassess the value of this protein as a tumour marker. Serum samples from 800 healthy individuals and patients with various benign and malignant diseases were assayed. There was a very wide range of alpha 2-PAG levels in normal females (1- greater than 100 mg/l), and although the levels found in normal males were lower and better defined, this intrinsic variation between individuals makes a single determination in a tumour-bearing patient meaningless. Also, the levels of alpha 1-PAG in patients with advanced cancer were not significantly different from levels in localized cancer, benign disease or even healthy controls, and furthermore, levels before and after successful cancer treatment did not show a significant change. Our results therefore indicate that alpha 2-PAG is unsuitable for use as a tumour marker as there was no apparent relationship between the levels of alpha 2-PAG and either tumour burden or response to treatment.
一种用于妊娠相关α-2糖蛋白(α2-PAG)的新型酶联免疫测定法的开发,为重新评估这种蛋白质作为肿瘤标志物的价值提供了契机。对800名健康个体以及患有各种良性和恶性疾病的患者的血清样本进行了检测。正常女性的α2-PAG水平范围非常广泛(1 - 大于100mg/L),尽管正常男性的水平较低且更明确,但个体之间的这种内在差异使得在肿瘤患者中进行单次测定毫无意义。此外,晚期癌症患者的α1-PAG水平与局部癌症、良性疾病甚至健康对照者的水平并无显著差异,而且,癌症成功治疗前后的水平也未显示出显著变化。因此,我们的结果表明,α2-PAG不适合用作肿瘤标志物,因为α2-PAG水平与肿瘤负荷或治疗反应之间没有明显关系。