DIFFERENTIAL EFFECT OF THE CALMODULIN INHIBITOR TRIFLUOPERAZINE ON CELLULAR ACCUMULATION, RETENTION, AND CYTO-TOXICITY OF ANTHRACYCLINES IN DOXORUBICIN (ADRIAMYCIN)-RESISTANT P388 MOUSE LEUKEMIA-CELLS

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  • 1 January 1984
    • journal article
    • research article
    • Vol. 44  (11) , 5056-5061
Abstract
Calmodulin inhibitors enhance cytotoxic effects of doxorubicin (DOX) in DOX-resistant (P388/DOX) P388 mouse leukemia cells by increasing cellular accumulation and retention of drug. In P388/DOX cells treated for 3 h, cytotoxic effects (based on colony formation in soft agar) of daunorubicin (DAU) in the presence of trifluoperazine (TFP) were DAU concentration-dependent and enhanced 2-100-fold. Additionally, in the presence of TFP, on a molar basis, equitoxic doses of DAU were 4-fold lower than DOX for P388/DOX cells. In P388/DOX cells treated for 3 h with other anthracyclines, except for a slight enhancement in the cytotoxic effects of aclacinomycin A (ACM) with TFP, colony formation in soft agar of cells treated with N-trifluoroacetyladriamycin-14-valerate (AD32) and N-trifluoroacetyladriamycin were similar in the absence and presence of TFP. In DOX-sensitive (P388/S) P388 mouse leukemia cells treated for 3 h, some enhancement in the cytotoxic effects due to TFP were observed with DAU and DOX, but not with ACM, AD32 or N-trifluoroacetyladriamycin. Although accumulation of ACM and AD32 in P388/S and P388/DOX cells was similar and unaffected by TFP, the retention of ACM but not AD32 was enhanced 1.5-fold only in TFP-treated P388/DOX cells. DAU accumulation in P388/S cells was 4-fold higher than in similarly treated P388/DOX cells and the 2- and 4-fold increase due to TFP in the accumulation and retention, respectively, of DAU in P388/DOX cells was not observed in P388/S cells. In P388/DOX cells, the calmodulin inhibitor TFP evidently is more effective with DAU than DOX, significantly less effective with ACM and ineffective with AD32 and N-trifluoroacetyladriamycin.