Relationship between cellular levels of beta-carotene and sensitivity to genotoxic agents
Abstract
The usefulness of an in vitro test system to predict the inhibitory effect of beta-carotene on the genotoxic activity of carcinogens/mutagens was explored. To facilitate the comparison of data obtained from cultured cells (CHO) and from exfoliated human cells, end-points were used which can be quantitated in both cell systems: the frequency of micronuclei for estimating the effect of genotoxic agents, and cellular levels of beta-carotene as a protective agent. In CHO cells, beta-carotene inhibited the clastogenic and micronu-cleus-forming effect of methyl methanesulfonate (MMS) and 4-nitroquinoline-l-oxide (4NQO), but had no protective action against gallic acid, tannic acid, an aqueous extract of areca nut or H2O2. The extent of inhibition depended on the ratio of beta-carotene to MMS. Doses of beta-carotene which exerted a protective effect in vitro ranged from approximately 2 to 5 ng per 106 CHO cells. Comparable levels of beta-carotene were previously found to reduce the frequency of micronucleated exfoliated cells from the buccal mu-cosa of tobacco and areca-nut chewers (Stich et al., 1984b).