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Consumption of high ω-3 fatty acid diet suppressed prostate tumorigenesis in C3(1) Tag mice
Prostate cancer incidence and mortality are high in the Western world and high ω-6/ω-3 PUFA in the Western diet may be a contributing factor. We investigated whether changing from a diet that approximates ω-6 fat content of the Western diet to a high ω-3 fat diet at adulthood might reduce prostate c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276330/ https://www.ncbi.nlm.nih.gov/pubmed/22045025 http://dx.doi.org/10.1093/carcin/bgr238 |
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author | Akinsete, Juliana A. Ion, Gabriela Witte, Theodore R. Hardman, W.Elaine |
author_facet | Akinsete, Juliana A. Ion, Gabriela Witte, Theodore R. Hardman, W.Elaine |
author_sort | Akinsete, Juliana A. |
collection | PubMed |
description | Prostate cancer incidence and mortality are high in the Western world and high ω-6/ω-3 PUFA in the Western diet may be a contributing factor. We investigated whether changing from a diet that approximates ω-6 fat content of the Western diet to a high ω-3 fat diet at adulthood might reduce prostate cancer risk. Female SV 129 mice that had consumed a high ω-6 diet containing corn oil for 2 weeks were bred with homozygous C3(1)Tag transgenic male mice. All male offspring were weaned to the corn oil diet (CO) until postpuberty when half of the male offspring were transferred to a high ω-3 diet containing canola oil and fish oil concentrate (FS). High ω-3 diet increased ω-3 and decreased ω-6 fat content of mice tissues. Average weights of prostate and genitourinary bloc were significantly lower in mice consuming high ω-3 diet at adulthood (CO-FS) than mice fed a lifetime high ω-6 diet (CO–CO). There was slower progression of tumorigenesis in dorsalateral prostate of CO-FS than in CO–CO mice. CO-FS mice had slightly lower plasma testosterone level at 24 and 40 weeks, significantly lower estradiol level at 40 weeks and significantly less expressed androgen receptor (AR) in the dorsalateral prostate at 40 weeks than CO–CO mice. Consumption of high ω-3 diet lowered the expression of genes expected to increase proliferation and decrease apoptosis in dorsalateral prostate. Our results suggest that consumption of high ω-3 diet slows down prostate tumorigenesis by lowering estradiol, testosterone and AR levels, promoting apoptosis and suppressing cell proliferation in C3(1)Tag mice. |
format | Online Article Text |
id | pubmed-3276330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32763302012-02-09 Consumption of high ω-3 fatty acid diet suppressed prostate tumorigenesis in C3(1) Tag mice Akinsete, Juliana A. Ion, Gabriela Witte, Theodore R. Hardman, W.Elaine Carcinogenesis Inflammation, Microenvironment and Prevention Prostate cancer incidence and mortality are high in the Western world and high ω-6/ω-3 PUFA in the Western diet may be a contributing factor. We investigated whether changing from a diet that approximates ω-6 fat content of the Western diet to a high ω-3 fat diet at adulthood might reduce prostate cancer risk. Female SV 129 mice that had consumed a high ω-6 diet containing corn oil for 2 weeks were bred with homozygous C3(1)Tag transgenic male mice. All male offspring were weaned to the corn oil diet (CO) until postpuberty when half of the male offspring were transferred to a high ω-3 diet containing canola oil and fish oil concentrate (FS). High ω-3 diet increased ω-3 and decreased ω-6 fat content of mice tissues. Average weights of prostate and genitourinary bloc were significantly lower in mice consuming high ω-3 diet at adulthood (CO-FS) than mice fed a lifetime high ω-6 diet (CO–CO). There was slower progression of tumorigenesis in dorsalateral prostate of CO-FS than in CO–CO mice. CO-FS mice had slightly lower plasma testosterone level at 24 and 40 weeks, significantly lower estradiol level at 40 weeks and significantly less expressed androgen receptor (AR) in the dorsalateral prostate at 40 weeks than CO–CO mice. Consumption of high ω-3 diet lowered the expression of genes expected to increase proliferation and decrease apoptosis in dorsalateral prostate. Our results suggest that consumption of high ω-3 diet slows down prostate tumorigenesis by lowering estradiol, testosterone and AR levels, promoting apoptosis and suppressing cell proliferation in C3(1)Tag mice. Oxford University Press 2012-01 2011-10-31 /pmc/articles/PMC3276330/ /pubmed/22045025 http://dx.doi.org/10.1093/carcin/bgr238 Text en © The Author 2011. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Inflammation, Microenvironment and Prevention Akinsete, Juliana A. Ion, Gabriela Witte, Theodore R. Hardman, W.Elaine Consumption of high ω-3 fatty acid diet suppressed prostate tumorigenesis in C3(1) Tag mice |
title | Consumption of high ω-3 fatty acid diet suppressed prostate tumorigenesis in C3(1) Tag mice |
title_full | Consumption of high ω-3 fatty acid diet suppressed prostate tumorigenesis in C3(1) Tag mice |
title_fullStr | Consumption of high ω-3 fatty acid diet suppressed prostate tumorigenesis in C3(1) Tag mice |
title_full_unstemmed | Consumption of high ω-3 fatty acid diet suppressed prostate tumorigenesis in C3(1) Tag mice |
title_short | Consumption of high ω-3 fatty acid diet suppressed prostate tumorigenesis in C3(1) Tag mice |
title_sort | consumption of high ω-3 fatty acid diet suppressed prostate tumorigenesis in c3(1) tag mice |
topic | Inflammation, Microenvironment and Prevention |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276330/ https://www.ncbi.nlm.nih.gov/pubmed/22045025 http://dx.doi.org/10.1093/carcin/bgr238 |
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