Hamada H, Okochi E, Watanabe M, Oh-hara T, Sugimoto Y, Kawabata H, Tsuruo T
Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Tokyo.
Cancer Res. 1988 Dec 15;48(24 Pt 1):7082-7.
For the characterization of membrane changes related to Adriamycin resistance in tumor cells, we have developed monoclonal antibodies against Adriamycin-resistant human myelogenous leukemia K562 (K562/ADM). In addition to the monoclonal antibodies which recognize P-glycoprotein, we have obtained two monoclonal antibodies (designated MRK4 and MRK20) which recognize an Mr 85,000 membrane protein. Using MRK20 as a probe, we have studied the expression of the Mr 85,000 protein in various human multidrug-resistant and -sensitive cell lines. The Mr 85,000 protein was overexpressed in K562/ADM and in a human ovarian cancer cell line resistant to Adriamycin, 2780AD. The protein, if any, was not detected in other drug-resistant human cell lines such as colchicine-resistant KB cells (KB-C4), vinblastine-resistant CEM cells (CEM/VLB100), and vincristine-resistant K562 cells (K562/VCR). We have isolated subclones of K562/ADM cells which express different amounts of the Mr 85,000 protein. The expression of the Mr 85,000 protein diminished when the cells were not kept in Adriamycin, and increased when the clones were kept in the presence of Adriamycin. In contrast, the expression of P-glycoprotein remained constant whether in the presence or absence of Adriamycin during these experiments. These findings suggest that the Mr 85,000 membrane protein is closely related to the resistant mechanism specific to Adriamycin resistance, which is different from that of the pleiotropic drug resistance.
为了表征肿瘤细胞中与阿霉素耐药相关的膜变化,我们制备了针对耐阿霉素的人髓性白血病K562(K562/ADM)的单克隆抗体。除了识别P-糖蛋白的单克隆抗体外,我们还获得了两种识别分子量为85,000的膜蛋白的单克隆抗体(命名为MRK4和MRK20)。使用MRK20作为探针,我们研究了分子量为85,000的蛋白在各种人多药耐药和敏感细胞系中的表达情况。分子量为85,000的蛋白在K562/ADM和对阿霉素耐药的人卵巢癌细胞系2780AD中过表达。在其他耐药人细胞系中,如耐秋水仙碱的KB细胞(KB-C4)、耐长春碱的CEM细胞(CEM/VLB100)和耐长春新碱的K562细胞(K562/VCR),未检测到该蛋白(如果有的话)。我们分离了K562/ADM细胞的亚克隆,这些亚克隆表达不同量的分子量为85,000的蛋白。当细胞不处于阿霉素环境中时,分子量为85,000的蛋白表达减少,而当克隆处于阿霉素存在的环境中时,该蛋白表达增加。相比之下,在这些实验中,无论有无阿霉素,P-糖蛋白的表达都保持恒定。这些发现表明,分子量为85,000的膜蛋白与阿霉素耐药特异性的耐药机制密切相关,这与多药耐药机制不同。