P388 leukaemia cells resistant to the anthracycline menogaril lack multidrug resistant phenotype

• Published in: British journal of cancer Vol. 62; no. 3; pp. 378 - 384
• Main Authors: BADINER, G. J, MOY, B. C, SMITH, K. S, TARPLEY, W. G, GROPPI, V. E, BHUYAN, D. K
• Format: Journal Article
• Language: English
• Published: Basingstoke Nature Publishing Group 01.09.1990
• Subjects: Animals; Antineoplastic Agents - pharmacology; Biological and medical sciences; Cell Division - drug effects; Cell Survival - drug effects; Cells, Cultured; Dose-Response Relationship, Drug; Doxorubicin - pharmacology; Drug Resistance - genetics; Drug Synergism; Glutathione - metabolism; Host-tumor relations. Immunology. Biological markers; In Vitro Techniques; Leukemia P388 - drug therapy; Leukemia P388 - genetics; Medical sciences; Menogaril; Mice; Nogalamycin - analogs & derivatives; Nogalamycin - pharmacokinetics; Nogalamycin - pharmacology; Tumors; Verapamil - pharmacology; Antineoplastic agent; Leukemia; Rodentia; Malignant hemopathy; In vitro; Resistance; Vertebrata; Phenotype; Mammalia; Mouse; Animal; Established cell line; Anthracyclins; Tumor cell
• ISSN: 0007-0920; 1532-1827
• DOI: 10.1038/bjc.1990.302

Menogaril is an anthracycline presently in Phase II clinical trials. Menogaril-resistant mouse leukaemia P388 cells were developed in vitro by 4 months of exposure to step-wise increasing concentrations of menogaril after which resistant cells (P388/MEN) were cloned in 320 ng ml-1 menogaril. P388/MEN cells were 40-fold more resistant to menogaril in vitro compared to P388/O and were also resistant in vivo. Resistance to menogaril was stable for at least 2 months in the absence of the drug. The results indicate that P388/MEN, although resistant to an anthracycline, did not display the typical multidrug resistant phenotype. It was not cross-resistant to several structurally unrelated drugs such as actinomycin D, cisplatin, or vinblastine, but it was cross-resistant to the anthracycline, adriamycin. Uptake and efflux of menogaril was similar in sensitive and resistant cell lines. Also, resistance was not reversed by verapamil. No major karyotypic difference was noted between P388/O and P388/MEN. There was no significant amplification or overexpression of the mdr gene in P388/MEN compared to P388/O. In contrast to P388/MEN, P388 cells resistant to adriamycin displayed the typical multidrug resistant phenotype. Glutathione content of P388/MEN cells was similar to that of P388/O and depletion of glutathione did not potentiate menogaril cytotoxicity. Therefore, we conclude that glutathione is not likely to be involved in menogaril resistance to P388/MEN cells.