The in vitro micronucleus assay for detection of cytogenetic effects induced by mutagen-carcinogens: comparison with the in vitro sister-chromatid exchange assay

Abstract

The sensitivity of a cytogenicic assay, as expressed by the in vitro induction of micronuclei (MN), was compared to the in vitro induction of sister-chromatid exchanges (SCEs). Chinese hamster lung (V79) cells were exposed to 3 known alkylating agents: methyl methanesulphonate (MMS), ethyl methanesulphonate (EMS) and N-methyl- N′-nitro- N-nitrosoguanidine (MNNG) andto 5 newly synthesized naphthofurans: 2-nitro-7-methoxynaphtho[2,1- b]furan (A), 2-nitro-8-methoxynaphtho[2,1- b]furan (B), 2-nitronaphto[2,1- b] furan (C), 2-nitro-7-bromonaphtho[2,1- b]furan (D) and 7-methoxynaphtho[2,1- b]furan (E). The induction of MN only was also analysed after exposure of the cells to 4 alcohols: ethanol, methanol, butanol and propanol. The lowest dose at which a significant effect could be observed ws determined. In both assays, MNNG, MMS and EMS were equally active with the following order of potency: MNNG > MMS > EMS, the latter being a very weak inducer of MN and SCE. Compounds A and B were also very effective in both assays. Compound C was a more active inducer of SCE than MN. Compounds D and E were not active in either assay. None of the 4 alcohols induced MN. Our results are compared with the previously published data on in vitro and in vivo induction of SCE and MN. We conclude that the MN in vitro assay which detects clastogens as well as agents affecting the spindle apparatus, is a good indicator of genotoxicity, though slightly less sensitive than the in vitro SCE test. It could provide a rapid, simple and inexpensive complementary short-term test for the evaluation of potentially mutagenic chemicals.