Hydroquinone (HQ) dose-dependently reduced the viable cell number of oral t
umor cell lines (HSC-2 MSG). He induced internucleosomal DNA fragmentation
in human promyelocytic leukemic HL-60 cells, but not in HSC-2 nor HSG cells
. Cytotoxic activity of HQ was slightly reduced by catalase, bill was enhan
ced by superoxide dismutase, suggesting the possible involvement of hydroge
n peroxide in HQ-induced cytotoxicity. This was supported by slight increas
e ol decrease of cytotoxicity of He in the presence of Cu2+ and Fe3+, respe
ctively. Lower concentrations of sodium ascorbate, ascorbic acid and ascorb
ic acid 6-palmitate reduced both the radical intensity and cytotoxic activi
ty of He, mole efficiently than ascorbic acid 2,6-dipalmitate, in contrast
to the cytotoxic action of these ascorbates at. higher (millimolar;) concen
trations. Popular antioxidants such as N-acetyl-L-cysteine and cysteine als
o reduced the radical intensity and cytotoxic activity of HQ The present st
udy suggests that cytotoxic activity of He is generated by radical-mediated
oxidation mechanism.