Lee C Y, Chen K W, Sheu F S, Tsang A, Chao K C, Ng H T
Department of Obstetrics and Gynecology, University of British Columbia, Vancouver, Canada.
Cancer Immunol Immunother. 1992;35(1):19-26. doi: 10.1007/BF01741050.
Monoclonal antibodies against an ovarian tumor cell line, OC-3-VGH, were generated using modified hybridoma technology. Among the seven that were selected for their high specificity and affinity to ovarian cancer cells and low cross-reactivity to most normal human tissues, RP 215 was shown to react specifically with a tumor-associated antigen, COX-1, from certain ovarian/cervical cancer cell lines. By Western blot assay, COX-1 was shown to have a subunit molecular mass of about 60 kDa and exist as an aggregate in the native state. COX-1 could also be detected in the shed medium of certain cultured tumor cells. A solid-phase sandwich enzyme-immunoassay procedure was designed for quantitative determinations of COX-1 in the shed medium or in patients' sera using RP 215 for both well-coating and the signal detection. Highly purified COX-1 was obtained from the shed medium of cultured OC-3-VGH tumor cells mainly by hydroxyapatite and immunoaffinity chromatography with RP 215 as the affinity ligand. At neutral pH, purified COX-1 also exists as an aggregate and is relatively stable at temperatures below 50 degrees C. Its immunoactivity was found to decrease with time in the presence of trypsin. However, the immunoactivity of COX-1 was not affected upon incubation with carbohydrate-digestive enzymes or concanavalin A and only partially inactivated in the presence of NaIO4 or iodoacetamide. Treatments of COX-1 with dithiothreitol and guanidine thiocyanate resulted in a complete loss of activity. Furthermore, rabbit antisera raised against purified COX-1 exhibited similar immunospecificity to that of RP 215. The results of this study suggest that COX-1 is a glycoprotein consisting of a 60 kDa subunit, which is recognized by RP 215 through its peptide determinant. Preliminary retrospective clinical studies were performed to assess the utility of a COX-1 enzyme immunoassay kit for detection and monitoring of patients with ovarian and cervical cancers.
利用改良的杂交瘤技术制备了针对卵巢肿瘤细胞系OC - 3 - VGH的单克隆抗体。在筛选出的七种对卵巢癌细胞具有高特异性和亲和力且对大多数正常人体组织交叉反应性低的抗体中,RP 215显示出与某些卵巢/宫颈癌细胞系中的一种肿瘤相关抗原COX - 1特异性反应。通过蛋白质免疫印迹分析,COX - 1显示出亚基分子量约为60 kDa,并且在天然状态下以聚集体形式存在。COX - 1也可以在某些培养的肿瘤细胞的脱落培养基中检测到。设计了一种固相夹心酶免疫分析方法,使用RP 215进行包被孔和信号检测,用于定量测定脱落培养基或患者血清中的COX - 1。主要通过羟基磷灰石和以RP 215为亲和配体的免疫亲和层析从培养的OC - 3 - VGH肿瘤细胞的脱落培养基中获得了高度纯化的COX - 1。在中性pH条件下,纯化的COX - 1也以聚集体形式存在,并且在低于50摄氏度的温度下相对稳定。发现其免疫活性在胰蛋白酶存在下随时间降低。然而,COX - 1与碳水化合物消化酶或伴刀豆球蛋白A孵育时免疫活性不受影响,在高碘酸钠或碘乙酰胺存在下仅部分失活。用二硫苏糖醇和硫氰酸胍处理COX - 1导致活性完全丧失。此外,针对纯化的COX - 1产生的兔抗血清表现出与RP 215相似的免疫特异性。本研究结果表明,COX - 1是一种由60 kDa亚基组成的糖蛋白,RP 215通过其肽决定簇识别该亚基。进行了初步回顾性临床研究,以评估COX - 1酶免疫分析试剂盒在检测和监测卵巢癌和宫颈癌患者中的效用。