Gros P, Ben Neriah Y B, Croop J M, Housman D E
Nature. 1986;323(6090):728-31. doi: 10.1038/323728a0.
The emergence and outgrowth of a population of tumour cells resistant to multiple drugs is a major problem in the chemotherapeutic treatment of cancer. We have used highly drug-resistant cell lines developed in vitro to study the molecular basis of multidrug resistance. In these cell lines high levels of resistance are frequently associated with amplification and overexpression of a small group of genes termed mdr or gp170. Direct evaluation of the role of these genes in multidrug resistance has awaited the isolation of a member of this gene family in a biologically active form. Here we report the isolation of DNA clones complementary to the cellular messenger RNA transcripts of mdr genes and show that high-level expression of a full-length complementary DNA clone in an otherwise drug-sensitive cell confers a complete multidrug-resistant phenotype. Our results demonstrate that overexpression of a single member of the mdr group is sufficient to confer drug resistance. Furthermore, because the cDNA was isolated from a drug-sensitive cell, mutations in the primary sequence of mdr are not required to produce a multidrug-resistance phenotype.
一群对多种药物耐药的肿瘤细胞的出现和增多是癌症化疗中的一个主要问题。我们利用体外培养的高度耐药细胞系来研究多药耐药的分子基础。在这些细胞系中,高水平的耐药性常常与一小群称为mdr或gp170的基因的扩增和过表达相关。对这些基因在多药耐药中作用的直接评估一直等待着以生物活性形式分离出该基因家族的一个成员。在此我们报告分离出与mdr基因的细胞信使RNA转录本互补的DNA克隆,并表明在一个原本对药物敏感的细胞中全长互补DNA克隆的高水平表达赋予了完全的多药耐药表型。我们的结果表明mdr组中单个成员的过表达就足以赋予耐药性。此外,由于该cDNA是从一个药物敏感细胞中分离出来的,产生多药耐药表型不需要mdr一级序列中的突变。