Fumonisin B(1) is genotoxic in human derived hepatoma (HepG2) cells
Veronika Ehrlich1, Firouz Darroudi, Maria Uhl
1Institute of Cancer Research, University of Vienna, Borschkegasse 8a, A-1090 Vienna, Austria.
Abstract:
Fumonisin B(1) (FB(1)), a widespread Fusarium toxin which is frequently found in corn, causes liver tumors in laboratory rodents and is a suspected human carcinogen. The compound was tested in micronucleus (MN) and single cell gel electrophoresis (SCGE) assays in human derived hepatoma (HepG2) cells and caused a pronounced dose-dependent genotoxic effect at exposure concentrations > or = 25 microg/ml. In contrast, no induction of his(+) revertants was found in Salmonella microsome assays with strains TA98, TA100, TA102, TA1535 and TA1537 upon addition of HepG2-derived enzyme (S9) mix in liquid incubation assays with identical exposure concentrations. Taken together, our results indicate that FB(1) is clastogenic in human derived cells. This observation supports the assumption that this compound may act as a genotoxic carcinogen in humans.
Insights
Fumonisin B(1) (FB(1)), a corn toxin, causes DNA damage in human liver cells. This genotoxic effect supports its suspected role as a human carcinogen.
Area of Science:
- Toxicology
- Genetics
- Carcinogenesis
Background:
- Fumonisin B(1) (FB(1)) is a widespread Fusarium toxin found in corn.
- FB(1) is known to cause liver tumors in rodents and is a suspected human carcinogen.
Purpose of the Study:
- To investigate the genotoxic potential of FB(1) in human-derived cells.
- To assess FB(1)'s clastogenic and mutagenic effects.
Main Methods:
- Micronucleus (MN) and single cell gel electrophoresis (SCGE) assays were performed on human hepatoma (HepG2) cells.
- Salmonella microsome assays (Ames test) with HepG2-derived S9 mix were conducted.
Main Results:
- FB(1) induced a dose-dependent genotoxic effect in HepG2 cells at concentrations ≥ 25 μg/ml.
- No mutagenic effect (his(+) revertants) was observed in Salmonella strains.
- FB(1) demonstrated clastogenic activity in human cells.
Conclusions:
- FB(1) is clastogenic in human-derived hepatoma cells.
- The findings support the hypothesis that FB(1) may act as a genotoxic carcinogen in humans.
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