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Gene rearrangement: a novel mechanism for MDR-1 gene activation.
L A Mickley, … , J L Biedler, T Fojo
L A Mickley, … , J L Biedler, T Fojo
Published April 15, 1997
Citation Information: J Clin Invest. 1997;99(8):1947-1957. https://doi.org/10.1172/JCI119362.
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Research Article

Gene rearrangement: a novel mechanism for MDR-1 gene activation.

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Abstract

Drug resistance, a major obstacle to cancer chemotherapy, can be mediated by MDR-1/P-glycoprotein. Deletion of the first 68 residues of MDR-1 in an adriamycin-selected cell line after a 4;7 translocation, t(4q;7q), resulted in a hybrid mRNA containing sequences from both MDR-1 and a novel chromosome 4 gene. Further selection resulted in amplification of a hybrid gene. Expression of the hybrid mRNA was controlled by the chromosome 4 gene, providing a model for overexpression of MDR-1. Additional hybrid mRNAs in other drug-selected cell lines and in patients with refractory leukemia, with MDR-1 juxtaposed 3' to an active gene, establishes random chromosomal rearrangements with overexpression of hybrid MDR-1 mRNAs as a mechanism of acquired drug resistance.

Authors

L A Mickley, B A Spengler, T A Knutsen, J L Biedler, T Fojo

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