Indications for a threshold of chemically‐induced aneuploidy in vitro in human lymphocytes

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Abstract
The possible existence of a threshold for compounds inducing chromosomal loss was investigated for four known aneugens (colchicine, COL; carben‐dazim, MBC; mebendazole, MEB; nocodazole, NOC) and two clastogens (methyl methanesulfo‐nate, MMS; mitomycin C, MMC) using the micronu‐cleus (MN) test in human lymphocytes. The presence of a whole chromosome in the MN was studied by fluorescent in situ hybridization (FISH) using a synthetic pancentromeric oligonucleotide probe. FISH was applied on two different MN preparations: cytokinesis‐blocked MN (MNCB) assay, and MN sorted by flow cytometry. At subtoxic concentrations analyzed by MNCB and FISH, COL, MEB, MBC, and NOC induced a concentration‐dependent increase in centromere‐positive MN (MNCen+), MMC seemed to induce an increase in both types of MN (MNCen‐ and MNCen+), while MMS induced only MNCen‐. On the sorted micronuclei (in a wide range of low to subtoxic concentrations), the concentration‐effect profile for MNCen+, with the four aneugens tested, showed a statistically nonsignificant increase over a range of concentrations, followed by a second range of high concentrations with a statistically significant increase. To analyze the existence of a threshold, a piecewise linear regression was applied to the data. The first concentration that showed a statistically significant increase in MNCen+ was chosen as a breakpoint (0.037 μM for COL, 2.62 μM for MBC, 0.27 μM for MEB, and 0.066 μM for NOC). The statistical correlation between observed and predicted values showed a high correlation (r = 0.99), indicating a clear threshold for aneuploidy induction. However, for MMS the concentration‐effect profile for MNCen+ showed a continuous concentration‐dependent decrease with no threshold. With the two cytotoxicity assays used (Bio‐Rad and MTT), no significant reduction was detected either in the protein content or in mitochondrial succinate dehydrogenase activity with all chemicals tested for MN induction. Therefore, our data suggest that the observed thresholds were not due to indirect toxic effects but to real aneugenic effects.