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Selenium-mediated inhibition of 7,12-dimethylbenz[a]anthracene-induced mouse mammary tumorigenesis
Abstract:
The effect of supplemental selenium on 7,12-dimethylbenz[a] anthracene (DMBA)-induced mammary tumorigenesis was investigated in several mouse strains. Selenium, administered as SeO2 in the drinking water, inhibited mammary tumor formation in DMBA-treated (C57BL x DBA/2f)F1, C3H/StWi and BALB/c female mice. In addition, selenium inhibited the occurrence of DMBA-induced ductal hyperplasias in (C57BL x DBA/2f)F1 and BALB/c mice and mammary tumour virus-induced alveolar hyperplasias in BALB/cfC3H mice. Selenium did not alter the growth of established mammary tumors. These results demonstrate that supplemental selenium inhibits both chemical-and viral-induced mouse mammary tumorigenesis, and secondly, that the development of preneoplastic lesions, an early stage in mammary tumorigenesis, is very sensitive to selenium-mediated inhibition.
Insights
Supplemental selenium inhibited mammary tumor formation and preneoplastic lesions in mice exposed to chemical carcinogens or viruses. Selenium did not affect established tumor growth, highlighting its preventative role.
Area of Science:
- Oncology
- Nutritional Science
- Carcinogenesis
Background:
- Mammary tumorigenesis is a complex process influenced by chemical and viral factors.
- Preneoplastic lesions represent an early, critical stage in tumor development.
- Selenium's role in cancer prevention warrants further investigation.
Purpose of the Study:
- To investigate the effect of supplemental selenium on 7,12-dimethylbenz[a]anthracene (DMBA)-induced mammary tumorigenesis.
- To determine if selenium can inhibit both chemical- and viral-induced mammary tumors and preneoplastic lesions.
- To assess selenium's impact on the growth of established mammary tumors.
Main Methods:
- Administration of selenium (SeO2) in drinking water to several mouse strains.
- Induction of mammary tumors using the chemical carcinogen DMBA.
- Investigation of mammary tumour virus-induced hyperplasias.
- Monitoring of tumor formation, preneoplastic lesions, and established tumor growth.
Main Results:
- Selenium significantly inhibited mammary tumor formation in DMBA-treated mice across multiple strains.
- Selenium reduced the occurrence of DMBA-induced ductal hyperplasias and viral-induced alveolar hyperplasias.
- Selenium supplementation did not influence the growth rate of pre-existing mammary tumors.
Conclusions:
- Supplemental selenium demonstrates potent inhibitory effects on both chemical and viral-induced mouse mammary tumorigenesis.
- The development of preneoplastic lesions is highly sensitive to selenium-mediated inhibition, suggesting a preventative role.
- Selenium may be a valuable agent for preventing mammary cancer initiation.