Literature DB >> 1969329

Transfer of adriamycin resistance by fusion of Mr 170,000 P-glycoprotein to the plasma membrane of sensitive cells.

J A Belli1, Y Zhang, P Fritz.   

Abstract

One of the characteristics of multidrug-resistant mammalian cells is the presence of a glycoprotein of approximately Mr 170,000 in their cell membrane. Termed P-glycoprotein, this glycoprotein is thought to be the gene product of an amplified gene cloned and sequenced from a cell line (LZ) which is highly resistant to Adriamycin and cross-resistant to actinomycin D, colchicine, and vincristine. Resistance to Adriamycin has been induced in sensitive cells by chromosome or gene transfer. We now show that P-glycoprotein isolated from LZ cells and fused to sensitive V79 Chinese hamster cells renders the latter transiently resistant to Adriamycin. Incorporation of P-glycoprotein was confirmed by immunoperoxidase staining of fusion products following treatment with antibody to P-glycoprotein and by Western blots of membrane preparations from fusion products. These results suggest that P-glycoprotein is one of the important factors in the expression of Adriamycin resistance and provide added confirmation that it may be the important product of gene amplification in multidrug-resistant cells. The results also suggest that the cell membrane may be one of several targets for Adriamycin cytotoxicity and that P-glycoprotein may be a binding site for Adriamycin, rendering the latter ineffective in registering sufficient membrane damage for cell killing.

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Year:  1990        PMID: 1969329

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  2 in total

1.  Different modalities of intercellular membrane exchanges mediate cell-to-cell p-glycoprotein transfers in MCF-7 breast cancer cells.

Authors:  Jennifer Pasquier; Ludovic Galas; Céline Boulangé-Lecomte; Damien Rioult; Florence Bultelle; Pierre Magal; Glenn Webb; Frank Le Foll
Journal:  J Biol Chem       Date:  2012-01-06       Impact factor: 5.157

2.  Comparison of (99m)Tc-sestamibi and doxorubicin to monitor inhibition of P-glycoprotein function.

Authors:  T Muzzammil; M J Moore; D Hedley; J R Ballinger
Journal:  Br J Cancer       Date:  2001-02-02       Impact factor: 7.640

  2 in total

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