Ellagic acid (EA), tannic acid (TA), caffeic acid (CA), and ferulic acid (F
A) offer considerable promise as anticarcinogens. The role of these dietary
polyphenols was investigated in the promotional phase of carcinogenesis. T
opical application of polyphenols simultaneously with phorbol-12-myristate-
13-acetate (PMA) or mezerein resulted in significant protection against 7,1
2-dimethylbenz[a]anthracene-induced skin tumors in mice. Caffeic acid was t
he most effective inhibitor of tumor promotion. In vivo and in vitro treatm
ent of murine peritoneal macrophages with the tumor promoters resulted in s
timulation of superoxide anion radical formation. Tannic acid, caffeic acid
, and ferulic acid were stranger inhibitors of PMA- and mezerein-induced su
peroxide anion radical than ellagic acid in in vivo and in vitro conditions
. Treatment of [1(3)-C-14]glycerol- or [methyl-'4C]choline chloride-labeled
resident or thioglycollate-elicited macrophages with PMA and mezerein led
to accumulation of radioactive diacylglycerol equivalents. The polyphenols
were capable of inhibiting these releases.