Shen D W, Fojo A, Roninson I B, Chin J E, Soffir R, Pastan I, Gottesman M M
Mol Cell Biol. 1986 Nov;6(11):4039-45. doi: 10.1128/mcb.6.11.4039-4045.1986.
Mouse NIH 3T3 cells were transformed to multidrug resistance with high-molecular-weight DNA from multidrug-resistant human KB carcinoma cells. The patterns of cross resistance to colchicine, vinblastine, and doxorubicin hydrochloride (Adriamycin; Adria Laboratories Inc.) of the human donor cell line and mouse recipients were similar. The multidrug-resistant human donor cell line contains amplified sequences of the mdr1 gene which are expressed at high levels. Both primary and secondary NIH 3T3 transformants contained and expressed these amplified human mdr1 sequences. Amplification and expression of the human mdr1 sequences and amplification of cotransferred human Alu sequences in the mouse cells correlated with the degree of multidrug resistance. These data suggest that the mdr1 gene is likely to be responsible for multidrug resistance in cultured cells.
用来自多药耐药的人KB癌细胞的高分子量DNA将小鼠NIH 3T3细胞转化为多药耐药。人供体细胞系和小鼠受体对秋水仙碱、长春碱和盐酸多柔比星(阿霉素;阿德里亚实验室公司)的交叉耐药模式相似。多药耐药的人供体细胞系含有mdr1基因的扩增序列,且高水平表达。原代和二代NIH 3T3转化体都含有并表达这些扩增的人mdr1序列。小鼠细胞中人mdr1序列的扩增和表达以及共转移的人Alu序列的扩增与多药耐药程度相关。这些数据表明mdr1基因可能是培养细胞中多药耐药的原因。