Lookup NU author(s): Dr Emma Meczes,
Dr Margaret Rogers,
Professor Caroline Austin
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Purpose: Methyl N-(4'-(9-acridinylamino)-phenyl)carbamate hydrochloride (AMCA) and methyl N-(4'-(9-acridinylamino)-2-methoxyphenyl)carbamate hydrochloride (mAMCA) are analogues of the topoisomerase II (topo II) poison amsacrine, and are distinguished from amsacrine by their high cytotoxicity towards non-cycling cells. Since mammalian cells contain two forms (α and β) of topo II and the α isoform is down-regulated in non-cycling cells, we have considered whether these carbamate analogues target topo IIβ selectively. Methods: A drug permeable yeast strain (JN394 top2-4) was transformed using a shuttle vector containing either human top2α, human top2α or yeast top2 under the control of a GAL1 promoter. The strain was analysed at a non-permissive temperature, where only the plasmid-borne topo II was active. Results: AMCA and mAMCA produced comparable levels of cell killing with human DNA topo IIα, human DNA topo IIβ and yeast DNA topo II. Two other acridine derivatives N-[2-(dimethylamino)ethyl]acridine-4- carboxamide (DACA) and its 7-chloro derivative, which like AMCA and mAMCA are able to overcome multidrug resistance mechanisms, were much more active against human DNA topo IIα than against human DNA topo IIβ and yeast DNA topo II. A series of mutant Chinese hamster and human lines with defined topo lesions, including the HL60/MX2 line that lacks topo IIβ expression, was also used to compare resistance to amsacrine, AMCA and etoposide. Loss of topo IIβ activity had a greater effect on amsacrine and AMCA than on etoposide. Resistance of murine Lewis lung cultures in exponential and plateau phase was also measured. Loss of topo IIα activity, as measured in both mutant cells expressing lower amounts of enzyme and in cells in plateau phase, resulted in concomitant acquisition of resistance that was greatest for etoposide and least for AMCA. Conclusion: We conclude that the carbamate analogues of amsacrine recognize both topo IIα and β in cells.
Author(s): Turnbull RM, Meczes EL, Rogers MP, Lock RB, Sullivan DM, Finlay GJ, Baguley BC, Austin CA
Publication type: Article
Publication status: Published
Journal: Cancer Chemotherapy and Pharmacology
Print publication date: 16/08/1999
ISSN (print): 0344-5704
ISSN (electronic): 1432-0843
PubMed id: 10447574
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