British Journal of Haematology · 1997 · 10 citations · 54 references
Hematological MalignancyLymphoid NeoplasiaB-cll CellsImmune Cell DevelopmentMixed-phenotype Acute LeukemiaMalignant Blood DisorderImmunologyHematologyPathologyMdr1 MrnaAutoimmunityAdult T-cell Leukemia-lymphomaImmunotherapyMedicineCell BiologyTumor BiologyMdr PhenotypeNormal B‐cell Homologue
B-cell chronic lymphocytic leukaemia (CLL) cells commonly express the multidrug resistance phenotype. The aim of this study was to establish whether the normal homologue in B-cell ontogeny of B-CLL also expressed the multidrug resistance (mdr) phenotype. Human tonsillar lymphocytes were sorted to yield two B-cell subsets based on the expression of CD19, CD5 and CD10. The normal homologue was represented by a population of B cells that was CD19 positive, CD10 negative and weakly expressed CD5. Based upon functional analysis and the detection of mdr1 mRNA by semi-quantitative PCR, these cells expressed the mdr phenotype. In contrast, functional multidrug resistance could not be demonstrated in CD19-positive CD10-positive cells with strong expression of CD5, nor could mdr1 mRNA be found in these cells. MRP was variably expressed in both B-cell subsets with no discernable differences in the pattern of expression. We conclude that normal B cells with a phenotype resembling that of B-CLL cells express the multidrug resistance phenotype.
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Expression of Multidrug Resistance Gene in Human Cancers
Lori J. Goldstein, Hanan Galski, Antonio Tito Fojo et al. · JNCI Journal of the National Cancer Institute · 1989 · 1.3K citations