Sarcophytol A (Sarp A), a nontoxic compound isolated from marine soft coral, inhibits the in vivo effects of
tumor promoters. However, the mechanism of its action is unknown. Our studies show that Sarp A suppresses
oxidant formation and
DNA oxidation in the epidermis of SENCAR mice exposed to 12-O-tetradecanoylphorbol-13-acetate (TPA). In the short-term experiments, mice were topically pretreated with different doses of Sarp A before 6.5 nmol TPA, and the same treatment was repeated 20 h later. Sarp A significantly decreased the TPA-induced infiltration of neutrophils, the levels of
myeloperoxidase in the dermis, and the formation of H2O2, cis-
thymidine glycol, 8-hydroxyl-2'-deoxyguanosine, and
5-hydroxymethyl-2'-deoxyuridine in the epidermis. In the long-term studies, repeated TPA applications (3.2 nmol twice a week for 16 weeks) increased cis-
thymidine glycol 2.7-fold,
5-hydroxymethyl-2'-deoxyuridine 3.4-fold, and 8-hydroxyl-2'-deoxyguanosine 3.3-fold in epidermal
DNA over the basal levels. Application of 350 nmol Sarp A before each TPA treatment significantly decreased the formation of oxidized
DNA bases even below those present in the control mouse skin. Histological examination showed that Sarp A also alleviated the TPA-induced inflammatory response and infiltration of phagocytes. Thus, it is possible that suppression of
tumor promotion by Sarp A is due (at least in part) to its inhibitory effects on
tumor promoter-mediated migration and activation of phagocytes,
oxidant formation, and
DNA base oxidation.