Three steroidal saponins showed higher cytotoxicity against human oral squa
mous cell carcinoma cell lines (HSC-2), as compared with normal human gingi
val fibroblasts HGF. Tumor specificity of saponins exceeded that of tannins
and flavonoids. Agarose gel electrophoresis showed that saponins failed to
induce internucleosomal DNA fragmentation, but produced large DNA fragment
s in both HSC-2 cells and human promyelocytic leukemic HL-60 cells. In cont
rast to epigallo-catechin gallate or gallic acid, cytotoxic activity of sap
onins was not significantly affected by metals (Co2+, Cu2+ Fe3+) nor by ant
ioxidants (sodium ascorbate, N-acetyl-L-cysteine, catalase). Furthermore, s
aponins did not produce radicals (detected by ESR spectroscopy) nor oxidati
on potential (measured by NO monitor). These data suggest that an oxidation
-mediated mechanism is not involved in the cytotoxicity induced by steroida
l saponins.