Ishii S, Naito M, Tsuruo T
Institute of Molecular and Cellular Biosciences, University of Tokyo.
Jpn J Cancer Res. 1993 Jul;84(7):776-82. doi: 10.1111/j.1349-7006.1993.tb02043.x.
Treatment of tumors with monoclonal antibodies against tumor antigen is one of the selective modalities for cancer therapy. We examined the therapeutic effect of MRK-20 (IgG1), a murine monoclonal antibody against resistance-associated 85-kDa membrane protein. The 85-kDa protein is expressed on the surface of multidrug-resistant cells induced by adriamycin. This protein is also expressed in some multiple-drug-resistant cells, including atypical multidrug-resistant cells. The protein, once lost during long-term culture without adriamycin, was rapidly induced by treatment with adriamycin but not with vinblastine or etoposide, suggesting a close relationship of the protein with adriamycin resistance but not with multidrug resistance. The antibody MRK-20 suppressed the growth of subcutaneously implanted tumors expressing the 85-kDa protein. Adriamycin-resistant human ovarian tumor 2780AD and innately resistant human erythroleukemia HEL cells in athymic mice were completely cured by treatment with MRK-20 antibody when the antibody was administered i.v. 2 days after s.c. tumor implantation. On the other hand, MRK-20 did not show any effect on the growth of the 85-kDa protein-negative A2780 human ovarian tumor. These results indicate that the effect of MRK-20 is highly specific to cells expressing 85-kDa protein.
用抗肿瘤抗原单克隆抗体治疗肿瘤是癌症治疗的选择性方法之一。我们检测了MRK - 20(IgG1)的治疗效果,它是一种针对耐药相关85kDa膜蛋白的鼠单克隆抗体。85kDa蛋白在阿霉素诱导的多药耐药细胞表面表达。该蛋白也在一些多药耐药细胞中表达,包括非典型多药耐药细胞。该蛋白在无阿霉素的长期培养过程中一旦丢失,用阿霉素处理可迅速诱导其表达,但长春碱或依托泊苷处理则不能,这表明该蛋白与阿霉素耐药密切相关,但与多药耐药无关。抗体MRK - 20抑制了皮下植入的表达85kDa蛋白的肿瘤生长。当在皮下肿瘤植入2天后静脉注射MRK - 20抗体时,无胸腺小鼠体内的阿霉素耐药人卵巢肿瘤2780AD和天然耐药的人红白血病HEL细胞被完全治愈。另一方面,MRK - 20对85kDa蛋白阴性的A2780人卵巢肿瘤生长没有任何影响。这些结果表明,MRK - 20的作用对表达85kDa蛋白的细胞具有高度特异性。