Ishikawa H, Kawano M M, Okada K, Tanaka H, Tanabe O, Sakai A, Asaoku H, Iwato K, Nobuyoshi M, Kuramoto A
Department of Internal Medicine, Hiroshima University, Japan.
Br J Haematol. 1993 Jan;83(1):68-74. doi: 10.1111/j.1365-2141.1993.tb04633.x.
In order to clarify the mechanism of drug resistance in human myeloma cells, we investigated the expressions of DNA topoisomerase I and topoisomerase II gene and the genes possibly related to drug resistance; multi-drug resistant gene 1 (MDR-1), glutathione S-transferase class pi gene (GST-pi), by Northern blotting. Myeloma cells in eight of 15 cases prior to chemotherapy expressed topoisomerase I mRNA considerably, while the expression of topoisomerase II mRNA was detected weakly in only one of 16 myeloma patients. There was not any correlation between expression of topoisomerase I mRNA and clinical drug resistance. Significant expression of MDR-1 mRNA and P-glycoprotein was not detected in 25 cases of multiple myeloma prior to chemotherapy and even after several courses of VAD (vincristine, adriamycin and dexamethasone) therapy by Northern blotting and immunostaining using monoclonal anti-P-glycoprotein antibody (MRK-16), respectively. On the other hand, 16 of 21 myeloma cases showed significant expression of GST-pi protein and GST-pi mRNA with the various strengths, but there was no apparent correlation between GST-pi mRNA expression and clinical response. Therefore these data suggest that expression of the genes we tested may not determine the level of drug resistance in multiple myeloma, but lower or no significant expression of topoisomerase II mRNA in most myeloma cells indicates the possibility that topoisomerase II inhibitors such as VP-16 and topoisomerase II-mediated cytotoxic drugs such as adriamycin, are not so effective for the treatment of multiple myeloma.
为了阐明人骨髓瘤细胞耐药的机制,我们通过Northern印迹法研究了DNA拓扑异构酶I和拓扑异构酶II基因以及可能与耐药相关的基因;多药耐药基因1(MDR-1)、谷胱甘肽S-转移酶π类基因(GST-π)的表达。15例化疗前骨髓瘤患者中有8例的骨髓瘤细胞大量表达拓扑异构酶I mRNA,而16例骨髓瘤患者中只有1例弱检测到拓扑异构酶II mRNA的表达。拓扑异构酶I mRNA的表达与临床耐药之间没有任何相关性。通过Northern印迹法以及分别使用单克隆抗P-糖蛋白抗体(MRK-16)进行免疫染色,在25例化疗前的多发性骨髓瘤病例中,甚至在接受几个疗程的VAD(长春新碱、阿霉素和地塞米松)治疗后,均未检测到MDR-1 mRNA和P-糖蛋白的显著表达。另一方面,21例骨髓瘤病例中有16例显示出不同强度的GST-π蛋白和GST-π mRNA的显著表达,但GST-π mRNA表达与临床反应之间没有明显相关性。因此这些数据表明,我们所检测基因的表达可能无法决定多发性骨髓瘤的耐药水平,但大多数骨髓瘤细胞中拓扑异构酶II mRNA表达较低或无显著表达表明,拓扑异构酶II抑制剂如依托泊苷以及拓扑异构酶II介导的细胞毒性药物如阿霉素,对多发性骨髓瘤的治疗可能不太有效。