Zyad A, Bénard J, Tursz T, Clarke R, Chouaib S
Laboratory of Immunology, URA 1156 CNRS, Villejuif, France.
Cancer Res. 1994 Feb 1;54(3):825-31.
The molecular basis of cross-resistance to tumor necrosis factor (TNF) and Adriamycin has been investigated using the breast adenocarcinoma cell line MCF7/p, its Adriamycin-resistant counterpart MCF7AdrR, and the MDR1 gene-transduced MCF-7 cells (MCF7/MDR1). While the parental cell line MCF7/p was TNF-sensitive, MCF7AdrR was TNF-resistant. The TNF resistance exhibited by MCF7AdrR cells was not due to a lack of TNF receptor expression because both cell lines express comparable levels of p75 and p55 receptors as revealed by immunofluorescence analysis. NF-kappa B translocation, which is an essential transducing signal of the TNF-induced lysis pathway, does not appear to be involved in this resistance as assessed by gel shift experiments. In order to determine the role of MDR1 gene expression in the development of this cross-resistance, MCF7/p cells transfected by the MDR1 gene were examined. Our data showed that the expression of the MDR1 gene in these cells resulted in a relative resistance of these cells to Adriamycin without affecting their susceptibility to TNF killing. The implication of the manganese superoxide dismutase and endogenous TNF expression in the cross-resistance by MCF7AdrR cells to Adriamycin and TNF has also been investigated. Northern blot analysis indicated that following TNF stimulation, the expression of 4-kilobase and 1-kilobase manganese superoxide dismutase mRNAs were 9- to 10-fold induced in MCF7AdrR cells as compared to MCF7/p and MCF7/MDR1 cells. This suggests a possible involvement of this enzyme in the Adriamycin-induced resistance to TNF. Although TNF-treatment of MCF7/p and MDR-cells induced endogenous TNF expression in these cells, the level of mRNA induction was selectively enhanced in MCF7AdrR cells (7- to 8-fold greater in MCF7AdrR cells as compared to MCF7/p and MCF7/MDR1 cells). Collectively, these data indicate that the expression of the MDR1 gene in MCF7/p cells following gene transfection is not sufficient for the acquisition of TNF resistance by MCF7/MDR1 cells. Furthermore, our data provide the first evidence that Adriamycin-induced resistance to TNF in MCF7AdrR cells may, in part, involve an overexpression of endogenous TNF and manganese superoxide dismutase genes.
利用乳腺癌细胞系MCF7/p、其阿霉素抗性对应细胞系MCF7AdrR以及多药耐药基因1(MDR1)转导的MCF-7细胞(MCF7/MDR1),对肿瘤坏死因子(TNF)和阿霉素交叉耐药的分子基础进行了研究。亲本细胞系MCF7/p对TNF敏感,而MCF7AdrR对TNF耐药。MCF7AdrR细胞表现出的TNF耐药并非由于缺乏TNF受体表达,因为免疫荧光分析显示这两种细胞系表达水平相当的p75和p55受体。凝胶迁移实验评估显示,作为TNF诱导细胞裂解途径的重要转导信号,核因子κB(NF-κB)易位似乎与这种耐药无关。为了确定MDR1基因表达在这种交叉耐药发生过程中的作用,对转染了MDR1基因的MCF7/p细胞进行了检测。我们的数据表明,这些细胞中MDR1基因的表达导致它们对阿霉素产生相对耐药性,而不影响它们对TNF杀伤的敏感性。还研究了锰超氧化物歧化酶和内源性TNF表达在MCF7AdrR细胞对阿霉素和TNF交叉耐药中的作用。Northern印迹分析表明,TNF刺激后,与MCF7/p和MCF7/MDR1细胞相比,MCF7AdrR细胞中4千碱基和1千碱基锰超氧化物歧化酶mRNA的表达被诱导了9至10倍。这表明该酶可能参与了阿霉素诱导的对TNF的耐药。尽管用TNF处理MCF7/p和MDR细胞会诱导这些细胞内源性TNF表达,但mRNA诱导水平在MCF7AdrR细胞中选择性增强(与MCF7/p和MCF7/MDR1细胞相比,MCF7AdrR细胞中高7至8倍)。总体而言,这些数据表明基因转染后MCF7/p细胞中MDR1基因的表达不足以使MCF7/MDR1细胞获得TNF耐药性。此外,我们的数据首次证明,MCF7AdrR细胞中阿霉素诱导的对TNF的耐药可能部分涉及内源性TNF和锰超氧化物歧化酶基因的过表达。