Abstract
The administration of estradiol propionate after the discontinuation of 1,2-dimethylhydrazine (DMH) treatment increased the incidence of uterine sarcoma in CBA mice from 32.5 (DMH alone) to 62.5%. The addition of the ascorbic acid (0.3% solution in drinking water) to estradiol propionate was followed by a decrease in the tumor incidence to 35%, i. e. the acid levelled the promoting effect of estradiol propionate almost completely. Sodium ascorbate did not share that effect. Mechanisms underlying the antiestrogenic effect of the ascorbic acid are discussed.
Publication types
-
Comparative Study
-
English Abstract
MeSH terms
-
1,2-Dimethylhydrazine
-
Animals
-
Ascorbic Acid / therapeutic use*
-
Carcinogens*
-
Dimethylhydrazines
-
Drug Interactions
-
Drug Screening Assays, Antitumor
-
Estradiol / analogs & derivatives*
-
Estradiol / toxicity
-
Estrogen Antagonists*
-
Female
-
Mice
-
Mice, Inbred CBA
-
Sarcoma, Experimental / chemically induced
-
Sarcoma, Experimental / mortality
-
Sarcoma, Experimental / prevention & control*
-
Uterine Neoplasms / chemically induced
-
Uterine Neoplasms / mortality
-
Uterine Neoplasms / prevention & control*
Substances
-
Carcinogens
-
Dimethylhydrazines
-
Estrogen Antagonists
-
Estradiol
-
1,2-Dimethylhydrazine
-
estradiol dipropionate
-
Ascorbic Acid