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Inhibitory effects of biochanin A on mouse lung tumor induced by benzo(a)pyrene.
Biochanin A, an isoflavone compound, is reported to have an inhibitory effect on benzo(a)pyrene [B(a)P] metabolism. We examined the modifying effect of biochanin A on in vivo carcinogenesis using a mouse lung tumor model. As carcinogens, a single subcutaneous injection of 0.5mg of B(a)P was given wi...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Korean Academy of Medical Sciences
1991
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049714/ https://www.ncbi.nlm.nih.gov/pubmed/1844641 |
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author | Lee, Y. S. Seo, J. S. Chung, H. T. Jang, J. J. |
author_facet | Lee, Y. S. Seo, J. S. Chung, H. T. Jang, J. J. |
author_sort | Lee, Y. S. |
collection | PubMed |
description | Biochanin A, an isoflavone compound, is reported to have an inhibitory effect on benzo(a)pyrene [B(a)P] metabolism. We examined the modifying effect of biochanin A on in vivo carcinogenesis using a mouse lung tumor model. As carcinogens, a single subcutaneous injection of 0.5mg of B(a)P was given within 24 hours after birth. The test groups were injected with 0.125mg of biochanin A in 0.1ml DMSO by i.p. 3 times a week for 6 weeks after weaning. All mice were sacrificed at week 9 and the incidence and multiplicity of lung tumors were examined. Concomitant administration of biochanin A showed a significant inhibitory effect on the incidence of tumor-bearing mice (12.5%, P < 0.01), as well as the mean number of tumors (0.13, P < 0.001), compared with the group treated with B(a)P alone in which the incidence was 57.1% and the mean number was 1.0. These results suggest that biochanin A has inhibitory potential on the development of mouse lung tumor induced by B(a)P. |
format | Text |
id | pubmed-3049714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-30497142011-03-09 Inhibitory effects of biochanin A on mouse lung tumor induced by benzo(a)pyrene. Lee, Y. S. Seo, J. S. Chung, H. T. Jang, J. J. J Korean Med Sci Research Article Biochanin A, an isoflavone compound, is reported to have an inhibitory effect on benzo(a)pyrene [B(a)P] metabolism. We examined the modifying effect of biochanin A on in vivo carcinogenesis using a mouse lung tumor model. As carcinogens, a single subcutaneous injection of 0.5mg of B(a)P was given within 24 hours after birth. The test groups were injected with 0.125mg of biochanin A in 0.1ml DMSO by i.p. 3 times a week for 6 weeks after weaning. All mice were sacrificed at week 9 and the incidence and multiplicity of lung tumors were examined. Concomitant administration of biochanin A showed a significant inhibitory effect on the incidence of tumor-bearing mice (12.5%, P < 0.01), as well as the mean number of tumors (0.13, P < 0.001), compared with the group treated with B(a)P alone in which the incidence was 57.1% and the mean number was 1.0. These results suggest that biochanin A has inhibitory potential on the development of mouse lung tumor induced by B(a)P. Korean Academy of Medical Sciences 1991-12 /pmc/articles/PMC3049714/ /pubmed/1844641 Text en |
spellingShingle | Research Article Lee, Y. S. Seo, J. S. Chung, H. T. Jang, J. J. Inhibitory effects of biochanin A on mouse lung tumor induced by benzo(a)pyrene. |
title | Inhibitory effects of biochanin A on mouse lung tumor induced by benzo(a)pyrene. |
title_full | Inhibitory effects of biochanin A on mouse lung tumor induced by benzo(a)pyrene. |
title_fullStr | Inhibitory effects of biochanin A on mouse lung tumor induced by benzo(a)pyrene. |
title_full_unstemmed | Inhibitory effects of biochanin A on mouse lung tumor induced by benzo(a)pyrene. |
title_short | Inhibitory effects of biochanin A on mouse lung tumor induced by benzo(a)pyrene. |
title_sort | inhibitory effects of biochanin a on mouse lung tumor induced by benzo(a)pyrene. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049714/ https://www.ncbi.nlm.nih.gov/pubmed/1844641 |
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