Differentiation and multidrug resistance in response to drug treatment in the K562 human leukaemia cell line |
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| Authors: | Denese C. Marks Mary W. Davey Ross A. Davey Antony D. Kidman |
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| Affiliation: | Neurobiology Unit, School of Biological and Biomedical Sciences, University of Technology, Sydney, Westbourne Street, Gore Hill, N.S.W.;Department of Clinical Oncology, Royal North Shore Hospital, St Leonards, N.S.W., Australia |
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| Abstract: | Summary. The relationship between differentiation and P-glycoprotein expression in response to chemotherapeutic drugs was studied in the K562 human leukaemia cell line by treatment with low, but clinically achievable levels of vinblastine and epirubicin. Resistant sublines were easily generated with the multidrug resistant phenotype being expressed in response to drug treatment as low as 1 ng/ml vinblastine and 10 ng/ml epirubicin. These sublines showed stable but heterogeneous expression of P-glycoprotein as revealed by immunocytochemistry, and confirmed by cloning. This heterogeneity was maintained over 18 months with intermittent drug treatment. While selection for resistance induced erythroid and myeloid differentiation, expression of P-glycoprotein was not correlated with the stem cell antigen CD34 or with specific markers of erythroid or myeloid differentiation. |
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