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. 1990 Jun;87(12):4737-41.
doi: 10.1073/pnas.87.12.4737.

Functional expression of murine multidrug resistance in Xenopus laevis oocytes

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Functional expression of murine multidrug resistance in Xenopus laevis oocytes

G Castillo et al. Proc Natl Acad Sci U S A. 1990 Jun.

Abstract

The development of multidrug resistance (MDR) is associated with the overproduction of a plasma membrane glycoprotein, P glycoprotein. Here we report the functional expression of a member of the murine mdr family of proteins and show that Xenopus oocytes injected with RNA encoding the mouse mdr1b P glycoprotein develop a MDR-like phenotype. Immunological analysis indicated that oocytes injected with the mdr1b RNA synthesized a protein with the size and immunological characteristics of the mouse mdr1b P glycoprotein. These oocytes exhibited a decreased accumulation of [3H]vinblastine and showed an increased capacity to extrude the drug compared to control oocytes not expressing the P glycoprotein. In addition, competition experiments indicated that verapamil, vincristine, daunomycin, and quinidine, but not colchicine, can overcome the rapid drug efflux conferred by the expression of the mouse P glycoprotein.

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References

    1. Nature. 1986 Oct 23-29;323(6090):728-31 - PubMed
    1. Nature. 1970 Aug 15;227(5259):680-5 - PubMed
    1. J Biol Chem. 1989 Aug 25;264(24):14376-81 - PubMed
    1. Annu Rev Biochem. 1989;58:137-71 - PubMed
    1. FASEB J. 1989 Dec;3(14):2583-92 - PubMed

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