Cole L A, Wang Y X, Elliott M, Latif M, Chambers J T, Chambers S K, Schwartz P E
Department of Obstetrics and Gynecology, Yale University School of Medicine, New Haven, Connecticut 06510.
Cancer Res. 1988 Mar 1;48(5):1356-60.
Many investigators have shown that a small proportion (13-36%) of subjects with nontrophoblastic gynecological cancers have elevated serum levels of human chorionic gonadotropin (hCG). The low proportion with detectable levels and the accompanying low titers have limited the use of hCG as a tumor marker. hCG is a glycoprotein composed of two noncovalently linked subunits (alpha and beta), which are the products of separate genes. With the intent of expanding the use of hCG as a tumor marker we investigated levels of hCG free beta-subunit and asialo free beta-subunit and its core glycopeptide (composed of beta-subunit residues 6-40 disulfide-linked to 55-92), collectively called urinary gonadotropin fragments (UGF), in healthy and cancer patients. An immunoradiometric assay was developed, using the core glycopeptide-directed antibody B204, that similarly measures the hCG free beta-subunit and the asialo free beta-subunit and its core glycopeptide. Parallel urine and serum samples were collected from 87 women with active gynecological cancer and hCG and UGF were measured. Just 18% of the women tested had detectable serum levels of hCG (greater than 0.2 ng/ml); none had elevated serum levels in the UGF assay (greater than 0.2 ng/ml). Of the same group, 32% had detectable urine hCG levels (mean titer, 0.50 ng/ml) and 74% exhibited elevated urinary levels in the UGF assay (mean titer, 2.0 ng/ml). In a control group (urines from 50 nonpregnant healthy women), 47 negative and three borderline positive results (0.30, 0.35, and 0.48 ng/ml) were observed in the UGF assay. These results suggested a sensitivity of 74% and specificity of 92% for the UGF test for gynecological cancers. By disease, 70% of those with cervical, 73% of those with ovarian, and 77% of those with endometrial cancers had detectable UGF levels (greater than 0.2 ng/ml). By stage, 50, 62, 75, 86, and 100% of those with stage 1, 2, 3, 4, or recurrent disease, respectively, had positive results. UGF is a promising new marker of gynecological malignancies.
许多研究人员表明,一小部分(13%-36%)非滋养细胞性妇科癌症患者的血清人绒毛膜促性腺激素(hCG)水平升高。可检测到hCG水平的比例较低且伴随的滴度也低,这限制了hCG作为肿瘤标志物的应用。hCG是一种糖蛋白,由两个非共价连接的亚基(α和β)组成,这两个亚基是不同基因的产物。为了扩大hCG作为肿瘤标志物的应用范围,我们研究了健康女性和癌症患者中游离β亚基hCG、去唾液酸游离β亚基hCG及其核心糖肽(由β亚基6-40位残基与55-92位残基通过二硫键连接而成)的水平,这些统称为尿促性腺激素片段(UGF)。利用针对核心糖肽的抗体B204开发了一种免疫放射分析方法,该方法同样可检测游离β亚基hCG、去唾液酸游离β亚基hCG及其核心糖肽。从87名患有活动性妇科癌症的女性中采集了平行的尿液和血清样本,并检测了hCG和UGF水平。仅18%的受试女性血清hCG水平可检测到(大于0.2 ng/ml);在UGF检测中,无人血清水平升高(大于0.2 ng/ml)。在同一组中,32%的女性尿液hCG水平可检测到(平均滴度为0.50 ng/ml),74%的女性在UGF检测中尿水平升高(平均滴度为2.0 ng/ml)。在一个对照组(50名未怀孕健康女性的尿液)中,UGF检测观察到47个阴性结果和3个临界阳性结果(0.30、0.35和0.48 ng/ml)。这些结果表明,UGF检测妇科癌症的敏感性为74%,特异性为92%。按疾病类型划分,70%的宫颈癌患者、73%的卵巢癌患者和77%的子宫内膜癌患者UGF水平可检测到(大于0.2 ng/ml)。按疾病分期划分,分别有50%、62%、75%、86%和100%的1期、2期、3期、4期或复发性疾病患者检测结果为阳性。UGF是一种很有前景的妇科恶性肿瘤新标志物。