Patterns of cross-sensitivity in the responses of clonal subpopulations isolated from the RIF-1 mouse sarcoma to selected nitrosoureas and nitrogen mustards

• Published in: British journal of cancer Vol. 50; no. 2; pp. 153 - 158
• Main Authors: REEVE, J. G, WRIGHT, K. A, WORKMAN, P
• Format: Journal Article
• Language: English
• Published: Basingstoke Nature Publishing Group 01-08-1984
• Subjects: Animals; Antineoplastic agents; Biological and medical sciences; Cell Survival - drug effects; Clone Cells - classification; Clone Cells - drug effects; General aspects; Medical sciences; Mice; Nitrogen Mustard Compounds - pharmacology; Nitrosourea Compounds - pharmacology; Pharmacology. Drug treatments; Ploidies; Sarcoma, Experimental - genetics; Sarcoma, Experimental - pathology; Antineoplastic agent; Vertebrata; Mammalia; Sensitivity resistance; Sarcoma; Mouse; Nitrosoureas; Animal; Rodentia; In vitro; Cell subpopulation; Tumor cell
• ISSN: 0007-0920; 1532-1827
• DOI: 10.1038/bjc.1984.157

The response of clonal subpopulations isolated from the RIF-1 mouse sarcoma to melphalan treatment is independent of cell ploidy, whereas a clear relationship exists between ploidy and cell sensitivity to CCNU treatment. In the present study RIF-1 clones have been exposed to nitrogen mustard, aniline mustard and chlorambucil, and to nitrosoureas BCNU, MeCCNU and chlorozotocin, in order to evaluate whether or not the different physiochemical and biological activities of these agents would affect the patterns of drug sensitivity obtained for melphalan and CCNU. Irrespective of the different lipophilicities, transport properties and chemical reactivities of the nitrogen mustards, RIF-1 clones showed the same pattern of sensitivity as previously observed for melphalan. Similarly, RIF-1 clones when exposed to nitrosoureas BCNU, MeCCNU and chlorozotocin, showed the same pattern of sensitivity as that obtained for CCNU exposure. These data suggest (a) that the variation in the sensitivity of RIF-1 clones to treatment by the nitrogen mustards is unlikely to reflect differences in either membrane permeability or in drug transport and (b) that the ploidy dependent nitrosourea responses shown by RIF-1 clones similarly do not reflect differences in drug uptake.