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Modulation of 7,12‐Dimethylbenz[a]anthracene‐induced Transmammary Carcinogenesis by Disulfiram and Butylated Hydroxyanisole in Mice

The individual as well as combined chemopreventive actions of disulfiram (DSF) and butylated hydroxyanisole (BHA) on 7,12‐dimethylbenz[a]anthracene (DMBA)‐induced transmammary car‐cinogenesis in mice were examined. When nursing mothers receiving normal diet were treated with DMBA (1 mg/mouse) on day...

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Detalles Bibliográficos
Autores principales: Rao, Araga Ramesha, Hussain, Syed Perwez, Jannu, Laxminarayana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1989
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917933/
https://www.ncbi.nlm.nih.gov/pubmed/2516846
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01650.x
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author Rao, Araga Ramesha
Hussain, Syed Perwez
Jannu, Laxminarayana
author_facet Rao, Araga Ramesha
Hussain, Syed Perwez
Jannu, Laxminarayana
author_sort Rao, Araga Ramesha
collection PubMed
description The individual as well as combined chemopreventive actions of disulfiram (DSF) and butylated hydroxyanisole (BHA) on 7,12‐dimethylbenz[a]anthracene (DMBA)‐induced transmammary car‐cinogenesis in mice were examined. When nursing mothers receiving normal diet were treated with DMBA (1 mg/mouse) on days 6, 8 and 10 postpartum, the tumor incidence in their 50‐week‐old F(1) progeny was 44.1%. When nursing mothers receiving 0.75% BHA diet, 0.5% DSF diet and 0.75% BHA+0.5% DSF diet were similarly treated with DMBA, the tumor incidences in their 50‐week‐old F(1) progeny were 14.7% (P<0.05), 12.5% (P<0.05) and 5.8% (P<0.01), respectively. It is concluded that diets containing BHA (0.75%) and DSF (0.5%), singly or in combination, can inhibit trans‐mammary carcinogenesis in Swiss albino mice.
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spelling pubmed-59179332018-05-11 Modulation of 7,12‐Dimethylbenz[a]anthracene‐induced Transmammary Carcinogenesis by Disulfiram and Butylated Hydroxyanisole in Mice Rao, Araga Ramesha Hussain, Syed Perwez Jannu, Laxminarayana Jpn J Cancer Res Article The individual as well as combined chemopreventive actions of disulfiram (DSF) and butylated hydroxyanisole (BHA) on 7,12‐dimethylbenz[a]anthracene (DMBA)‐induced transmammary car‐cinogenesis in mice were examined. When nursing mothers receiving normal diet were treated with DMBA (1 mg/mouse) on days 6, 8 and 10 postpartum, the tumor incidence in their 50‐week‐old F(1) progeny was 44.1%. When nursing mothers receiving 0.75% BHA diet, 0.5% DSF diet and 0.75% BHA+0.5% DSF diet were similarly treated with DMBA, the tumor incidences in their 50‐week‐old F(1) progeny were 14.7% (P<0.05), 12.5% (P<0.05) and 5.8% (P<0.01), respectively. It is concluded that diets containing BHA (0.75%) and DSF (0.5%), singly or in combination, can inhibit trans‐mammary carcinogenesis in Swiss albino mice. Blackwell Publishing Ltd 1989-12 /pmc/articles/PMC5917933/ /pubmed/2516846 http://dx.doi.org/10.1111/j.1349-7006.1989.tb01650.x Text en
spellingShingle Article
Rao, Araga Ramesha
Hussain, Syed Perwez
Jannu, Laxminarayana
Modulation of 7,12‐Dimethylbenz[a]anthracene‐induced Transmammary Carcinogenesis by Disulfiram and Butylated Hydroxyanisole in Mice
title Modulation of 7,12‐Dimethylbenz[a]anthracene‐induced Transmammary Carcinogenesis by Disulfiram and Butylated Hydroxyanisole in Mice
title_full Modulation of 7,12‐Dimethylbenz[a]anthracene‐induced Transmammary Carcinogenesis by Disulfiram and Butylated Hydroxyanisole in Mice
title_fullStr Modulation of 7,12‐Dimethylbenz[a]anthracene‐induced Transmammary Carcinogenesis by Disulfiram and Butylated Hydroxyanisole in Mice
title_full_unstemmed Modulation of 7,12‐Dimethylbenz[a]anthracene‐induced Transmammary Carcinogenesis by Disulfiram and Butylated Hydroxyanisole in Mice
title_short Modulation of 7,12‐Dimethylbenz[a]anthracene‐induced Transmammary Carcinogenesis by Disulfiram and Butylated Hydroxyanisole in Mice
title_sort modulation of 7,12‐dimethylbenz[a]anthracene‐induced transmammary carcinogenesis by disulfiram and butylated hydroxyanisole in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917933/
https://www.ncbi.nlm.nih.gov/pubmed/2516846
http://dx.doi.org/10.1111/j.1349-7006.1989.tb01650.x
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