Sekine H, Hayes D F, Ohno T, Keefe K A, Schaetzl E, Bast R C, Knapp R, Kufe D W
J Clin Oncol. 1985 Oct;3(10):1355-63. doi: 10.1200/JCO.1985.3.10.1355.
The murine monoclonal antibody (MAb), designated DF3, reacts with a 300-kilodalton (kd) mammary epithelial antigen. A sequential double-determinant enzyme-linked immunoassay (EIA) has been developed to monitor circulating DF3 antigen. Previous studies have demonstrated that the use of the DF3 EIA provides a new and potentially useful marker to follow the clinical course of patients with metastatic breast cancer. In the present study, we have monitored circulating DF3 antigen in the serum of patients with epithelial ovarian carcinomas and non-ovarian gynecologic malignancies. Twenty-one of 45 patients (47%) with ovarian carcinoma had elevated DF3 antigen levels (greater than or equal to 30 U/mL). In contrast, three of 20 patients (15%) with non-ovarian gynecologic malignancies, and only four of 59 control women (7%) had elevation of circulating DF3 antigen. The difference between DF3 antigen values from patients with ovarian cancer and from controls was significant (P less than .001). The elevation of circulating DF3 antigen in ovarian cancer patients has also been confirmed by transblot assays. MAb DF3 reactivity occurred predominately with circulating antigens of molecular weights (mol wt) ranging from 300 to 450 kd. Furthermore, DF3 antigen levels have been shown to correlate with progression of disease in six patients with ovarian cancer and after resection of disease in two others. The half-life of circulating DF3 antigen was approximately 45 to 60 days. The results also demonstrate that DF3 antigen is distinct from CA125, a glycoprotein associated with coelomic epithelium and developmental amnion. The use of both the DF3 EIA and the immunoradiometric assay previously described to detect circulating CA125 suggests that determining levels of both markers may enhance the sensitivity of monitoring the course of ovarian cancer. Furthermore, the use of both assays may be useful in distinguishing ovarian cancer from other malignancies.
名为DF3的鼠单克隆抗体(MAb)可与一种300千道尔顿(kd)的乳腺上皮抗原发生反应。已开发出一种连续双决定簇酶联免疫分析(EIA)来监测循环中的DF3抗原。先前的研究表明,使用DF3 EIA可为追踪转移性乳腺癌患者的临床病程提供一种新的、可能有用的标志物。在本研究中,我们监测了上皮性卵巢癌和非卵巢妇科恶性肿瘤患者血清中的循环DF3抗原。45例卵巢癌患者中有21例(47%)的DF3抗原水平升高(大于或等于30 U/mL)。相比之下,20例非卵巢妇科恶性肿瘤患者中有3例(15%),59例对照女性中仅有4例(7%)的循环DF3抗原升高。卵巢癌患者与对照组的DF3抗原值差异显著(P小于0.001)。转印分析也证实了卵巢癌患者循环DF3抗原的升高。MAb DF3主要与分子量(mol wt)在300至450 kd范围内的循环抗原发生反应。此外,已证明DF3抗原水平与6例卵巢癌患者的疾病进展以及另外2例患者疾病切除后相关。循环DF3抗原的半衰期约为45至60天。结果还表明,DF3抗原与CA125不同,CA125是一种与体腔上皮和发育中的羊膜相关的糖蛋白。使用DF3 EIA和先前描述的免疫放射分析来检测循环中的CA125表明,测定两种标志物的水平可能会提高监测卵巢癌病程的敏感性。此外,两种检测方法的联合使用可能有助于区分卵巢癌与其他恶性肿瘤。