Regression of experimental cancer by oral administration of combined α‐tocopherol and β‐carotene
- 1 January 1989
- journal article
- other
- Published by Taylor & Francis in Nutrition and Cancer
- Vol. 12 (4) , 321-325
- https://doi.org/10.1080/01635588909514032
Abstract
α‐Tocopherol (vitamin E) and β‐carotene have been shown to be capable of regressing established epidermoid carcinomas of hamster buccal pouch when injected locally into the tumor site. Neither has yet been shown to be effective in regressing cancer when adminstered by oral route. However, a combination of both α‐tocopherol and β‐carotene was shown to be effective in regressing epidermoid carcinomas of hamster buccal pouch when the mixture was adminstered orally in vegetable oil. The epidermoid carcinomas were induced in the right buccal pouch of 100 Syrian hamsters by painting three times weekly for 14 weeks with a 0.5% solution of 7,12‐dimethylbenz[a]an‐thracene in mineral oil. The animals were then divided into five equal groups of 20 animals. Group 1 animals received no further treatment and represented tumor controls. Group 2 animals received 200 μg β‐carotene and 200 μg dl‐α‐tocopherol acid succinate combined in 0.2 ml vegetable oil. Animals received the mixture daily by mouth using a 1 ‐ml syringe. Groups 3 and 4 received β‐carotene and α‐tocopherol individually in double amounts (400 μg in 0.2 ml vegetable oil). Group 5 animals received only the vegetable oil (0.2 ml daily) and were controls for vehicle. The animals in Groups 1,3,4, and 5 were killed after 22 weeks because the tumors were extensive, large, and necrotic and the animals were weak and cachectic. After 22 weeks, the tumors in Group 2 animals were small in 15 out of 20 animals. The tumors were reduced in size compared with tumor burden at 14 weeks, the point at which the β‐carotene/α‐tocopherol was started.Keywords
This publication has 11 references indexed in Scilit:
- Regression of experimental oral carcinomas by local injection of β‐carotene and canthaxanthinNutrition and Cancer, 1988
- GGT reduction in beta carotene-inhibition of hamster buccal pouch carcinogenesisEuropean Journal of Cancer and Clinical Oncology, 1986
- Beta carotene is associated with the regression of hamster buccal pouch carcinoma and the induction of tumor necrosis factor in macrophagesBiochemical and Biophysical Research Communications, 1986
- Inhibition of experimental oral carcinogenesis by topical beta caroteneCarcinogenesis: Integrative Cancer Research, 1986
- Vitamin E stimulates proliferation of experimental oral carcinoma cellsin vitroNutrition and Cancer, 1986
- Retardation of experimental oral cancer by topical vitamin ENutrition and Cancer, 1985
- β-Carotene: an Unusual Type of Lipid AntioxidantScience, 1984
- Vitamin E inhibition of hamster buccal pouch carcinogenesis: A gross, histologic, and ultrastructural studyOral Surgery, Oral Medicine, Oral Pathology, 1982
- Effect of K3T3 sarcomas on tissue concentrations of vitamin ENutrition and Cancer, 1982
- Direct observation of a free radical interaction between vitamin E and vitamin CNature, 1979