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Beneficial bacteria stimulate host immune cells to counteract dietary and genetic predisposition to mammary cancer in mice
Recent studies suggest health benefits including protection from cancer after eating fermented foods such as probiotic yogurt, though the mechanisms are not well understood. Here we tested mechanistic hypotheses using two different animal models: the first model studied development of mammary cancer...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131439/ https://www.ncbi.nlm.nih.gov/pubmed/24382758 http://dx.doi.org/10.1002/ijc.28702 |
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author | Lakritz, Jessica R Poutahidis, Theofilos Levkovich, Tatiana Varian, Bernard J Ibrahim, Yassin M Chatzigiagkos, Antonis Mirabal, Sheyla Alm, Eric J Erdman, Susan E |
author_facet | Lakritz, Jessica R Poutahidis, Theofilos Levkovich, Tatiana Varian, Bernard J Ibrahim, Yassin M Chatzigiagkos, Antonis Mirabal, Sheyla Alm, Eric J Erdman, Susan E |
author_sort | Lakritz, Jessica R |
collection | PubMed |
description | Recent studies suggest health benefits including protection from cancer after eating fermented foods such as probiotic yogurt, though the mechanisms are not well understood. Here we tested mechanistic hypotheses using two different animal models: the first model studied development of mammary cancer when eating a Westernized diet, and the second studied animals with a genetic predilection to breast cancer. For the first model, outbred Swiss mice were fed a Westernized chow putting them at increased risk for development of mammary tumors. In this Westernized diet model, mammary carcinogenesis was inhibited by routine exposure to Lactobacillus reuteri ATCC-PTA-6475 in drinking water. The second model was FVB strain erbB2 (HER2) mutant mice, genetically susceptible to mammary tumors mimicking breast cancers in humans, being fed a regular (non-Westernized) chow diet. We found that oral supplement with these purified lactic acid bacteria alone was sufficient to inhibit features of mammary neoplasia in both models. The protective mechanism was determined to be microbially-triggered CD4+CD25+ lymphocytes. When isolated and transplanted into other subjects, these L. reuteri-stimulated lymphocytes were sufficient to convey transplantable anti-cancer protection in the cell recipient animals. These data demonstrate that host immune responses to environmental microbes significantly impact and inhibit cancer progression in distal tissues such as mammary glands, even in genetically susceptible mice. This leads us to conclude that consuming fermentative microbes such as L. reuteri may offer a tractable public health approach to help counteract the accumulated dietary and genetic carcinogenic events integral in the Westernized diet and lifestyle. WHAT'S NEW? Can eating fermented foods like yogurt ward off cancer? Recent studies have suggested it's possible. To find out how, these authors isolated the probiotic bacteria involved in fermentation and fed them to mice that were susceptible to mammary tumors. These mice either had genetic changes predisposing them to cancer or were fed a diet known to increase their likelihood of developing the tumors. Eating the lactic acid bacteria stimulated an immune response that delayed the onset of tumors in both models, suggesting a potential avenue to prevent the cancer in humans. |
format | Online Article Text |
id | pubmed-4131439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41314392014-12-03 Beneficial bacteria stimulate host immune cells to counteract dietary and genetic predisposition to mammary cancer in mice Lakritz, Jessica R Poutahidis, Theofilos Levkovich, Tatiana Varian, Bernard J Ibrahim, Yassin M Chatzigiagkos, Antonis Mirabal, Sheyla Alm, Eric J Erdman, Susan E Int J Cancer Carcinogenesis Recent studies suggest health benefits including protection from cancer after eating fermented foods such as probiotic yogurt, though the mechanisms are not well understood. Here we tested mechanistic hypotheses using two different animal models: the first model studied development of mammary cancer when eating a Westernized diet, and the second studied animals with a genetic predilection to breast cancer. For the first model, outbred Swiss mice were fed a Westernized chow putting them at increased risk for development of mammary tumors. In this Westernized diet model, mammary carcinogenesis was inhibited by routine exposure to Lactobacillus reuteri ATCC-PTA-6475 in drinking water. The second model was FVB strain erbB2 (HER2) mutant mice, genetically susceptible to mammary tumors mimicking breast cancers in humans, being fed a regular (non-Westernized) chow diet. We found that oral supplement with these purified lactic acid bacteria alone was sufficient to inhibit features of mammary neoplasia in both models. The protective mechanism was determined to be microbially-triggered CD4+CD25+ lymphocytes. When isolated and transplanted into other subjects, these L. reuteri-stimulated lymphocytes were sufficient to convey transplantable anti-cancer protection in the cell recipient animals. These data demonstrate that host immune responses to environmental microbes significantly impact and inhibit cancer progression in distal tissues such as mammary glands, even in genetically susceptible mice. This leads us to conclude that consuming fermentative microbes such as L. reuteri may offer a tractable public health approach to help counteract the accumulated dietary and genetic carcinogenic events integral in the Westernized diet and lifestyle. WHAT'S NEW? Can eating fermented foods like yogurt ward off cancer? Recent studies have suggested it's possible. To find out how, these authors isolated the probiotic bacteria involved in fermentation and fed them to mice that were susceptible to mammary tumors. These mice either had genetic changes predisposing them to cancer or were fed a diet known to increase their likelihood of developing the tumors. Eating the lactic acid bacteria stimulated an immune response that delayed the onset of tumors in both models, suggesting a potential avenue to prevent the cancer in humans. BlackWell Publishing Ltd 2014-08-01 2013-12-31 /pmc/articles/PMC4131439/ /pubmed/24382758 http://dx.doi.org/10.1002/ijc.28702 Text en © 2013 The Authors. Published by Wiley Periodicals, Inc. on behalf of UICC http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Carcinogenesis Lakritz, Jessica R Poutahidis, Theofilos Levkovich, Tatiana Varian, Bernard J Ibrahim, Yassin M Chatzigiagkos, Antonis Mirabal, Sheyla Alm, Eric J Erdman, Susan E Beneficial bacteria stimulate host immune cells to counteract dietary and genetic predisposition to mammary cancer in mice |
title | Beneficial bacteria stimulate host immune cells to counteract dietary and genetic predisposition to mammary cancer in mice |
title_full | Beneficial bacteria stimulate host immune cells to counteract dietary and genetic predisposition to mammary cancer in mice |
title_fullStr | Beneficial bacteria stimulate host immune cells to counteract dietary and genetic predisposition to mammary cancer in mice |
title_full_unstemmed | Beneficial bacteria stimulate host immune cells to counteract dietary and genetic predisposition to mammary cancer in mice |
title_short | Beneficial bacteria stimulate host immune cells to counteract dietary and genetic predisposition to mammary cancer in mice |
title_sort | beneficial bacteria stimulate host immune cells to counteract dietary and genetic predisposition to mammary cancer in mice |
topic | Carcinogenesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131439/ https://www.ncbi.nlm.nih.gov/pubmed/24382758 http://dx.doi.org/10.1002/ijc.28702 |
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