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Cytotoxicity of lysomustine and its isomers, and their potential use for selection of cells

Identifieur interne : 002571 ( Main/Exploration ); précédent : 002570; suivant : 002572

Cytotoxicity of lysomustine and its isomers, and their potential use for selection of cells

Auteurs : F. N. Rozov [Russie] ; T. S. Grinenko [Russie] ; G. L. Levit [Russie] ; A. N. Grishakov [Russie] ; A. V. Belyavsky [Russie] ; V. P. Krasnov [Russie]

Source :

RBID : ISTEX:8E9475CA937E7AE9200823D4BE50382D5475EF24

English descriptors

Abstract

Abstract: N ɛ-Nitroso-N ɛ-[N′-(2-chloroethyl)carbamoyl]-L-lysine (I) and N ɛ-[N′-(2-chloroethyl)-N′-nitrosocarbamoyl]-L-lysine (II), the isomers being the constituents of antitumor agent lysomustine, were isolated from the agent by reverse phase HPLC (RP-HPLC). The study of cytotoxicity of the above compounds against K562 cells showed that lesions induced by isomer (II) produce a significant cytotoxic effect, but can be efficiently repaired by the action of MGMT (O6-methylguanine-DNA methyltransferase). Under similar conditions, lesions induced by isomer (I) produce a substantially smaller effect but are weakly, if at all, repairable by MGMT. The effects of a clinically approved agent lysomustine, which is a mixture of isomers (I) and (II), are similar to those of isomer (II). The results obtained point to a different chemical nature of DNA lesions induced by two lysomustine isomers. Our data indicate that lysomustine and its isomer (II) can be used for in vitro selection of cells expressing MGMT.

Url:
DOI: 10.1134/S1068162011060112


Affiliations:


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<div type="abstract" xml:lang="en">Abstract: N ɛ-Nitroso-N ɛ-[N′-(2-chloroethyl)carbamoyl]-L-lysine (I) and N ɛ-[N′-(2-chloroethyl)-N′-nitrosocarbamoyl]-L-lysine (II), the isomers being the constituents of antitumor agent lysomustine, were isolated from the agent by reverse phase HPLC (RP-HPLC). The study of cytotoxicity of the above compounds against K562 cells showed that lesions induced by isomer (II) produce a significant cytotoxic effect, but can be efficiently repaired by the action of MGMT (O6-methylguanine-DNA methyltransferase). Under similar conditions, lesions induced by isomer (I) produce a substantially smaller effect but are weakly, if at all, repairable by MGMT. The effects of a clinically approved agent lysomustine, which is a mixture of isomers (I) and (II), are similar to those of isomer (II). The results obtained point to a different chemical nature of DNA lesions induced by two lysomustine isomers. Our data indicate that lysomustine and its isomer (II) can be used for in vitro selection of cells expressing MGMT.</div>
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