Affiliation: | a Neurobiology Unit, School of Biological and Biomedical Sciences, University of Technology, Sydney, Westbourne Street, Gore Hill, N.S.W., 2065, Australia * Department of Clinical Oncology, Royal North Shore Hospital, St Leonards, N.S.W., 2065, Australia |
Abstract: | The MTT cell viability assay is widely used in determining drug sensitivity profiles for patients with hematological malignancies and in primary screening of potential chemotherapeutic drugs. Because the multidrug resistance (MDR) phenotype is associated with these malignancies, and since many vital dyes are effluxed from MDR expressing cells, we have investigated whether the MDR phenotype interferes with the MTT assay. In CCRF-CEM and K562 human leukemic cell lines and drug-resistant sub-lines developed from them, comparison of the MTT assay with other cell viability assays showed significant variation in 50 concentrations, although the resistance relative to the sensitive parent cell was correlated. Inclusion of verapamil, an inhibitor of drug efflux activity, had no effect an the MTT assay. |