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Microbial Dysbiosis Is Associated with Human Breast Cancer

Breast cancer affects one in eight women in their lifetime. Though diet, age and genetic predisposition are established risk factors, the majority of breast cancers have unknown etiology. The human microbiota refers to the collection of microbes inhabiting the human body. Imbalance in microbial comm...

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Autores principales: Xuan, Caiyun, Shamonki, Jaime M., Chung, Alice, DiNome, Maggie L., Chung, Maureen, Sieling, Peter A., Lee, Delphine J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885448/
https://www.ncbi.nlm.nih.gov/pubmed/24421902
http://dx.doi.org/10.1371/journal.pone.0083744
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author Xuan, Caiyun
Shamonki, Jaime M.
Chung, Alice
DiNome, Maggie L.
Chung, Maureen
Sieling, Peter A.
Lee, Delphine J.
author_facet Xuan, Caiyun
Shamonki, Jaime M.
Chung, Alice
DiNome, Maggie L.
Chung, Maureen
Sieling, Peter A.
Lee, Delphine J.
author_sort Xuan, Caiyun
collection PubMed
description Breast cancer affects one in eight women in their lifetime. Though diet, age and genetic predisposition are established risk factors, the majority of breast cancers have unknown etiology. The human microbiota refers to the collection of microbes inhabiting the human body. Imbalance in microbial communities, or microbial dysbiosis, has been implicated in various human diseases including obesity, diabetes, and colon cancer. Therefore, we investigated the potential role of microbiota in breast cancer by next-generation sequencing using breast tumor tissue and paired normal adjacent tissue from the same patient. In a qualitative survey of the breast microbiota DNA, we found that the bacterium Methylobacterium radiotolerans is relatively enriched in tumor tissue, while the bacterium Sphingomonas yanoikuyae is relatively enriched in paired normal tissue. The relative abundances of these two bacterial species were inversely correlated in paired normal breast tissue but not in tumor tissue, indicating that dysbiosis is associated with breast cancer. Furthermore, the total bacterial DNA load was reduced in tumor versus paired normal and healthy breast tissue as determined by quantitative PCR. Interestingly, bacterial DNA load correlated inversely with advanced disease, a finding that could have broad implications in diagnosis and staging of breast cancer. Lastly, we observed lower basal levels of antibacterial response gene expression in tumor versus healthy breast tissue. Taken together, these data indicate that microbial DNA is present in the breast and that bacteria or their components may influence the local immune microenvironment. Our findings suggest a previously unrecognized link between dysbiosis and breast cancer which has potential diagnostic and therapeutic implications.
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spelling pubmed-38854482014-01-13 Microbial Dysbiosis Is Associated with Human Breast Cancer Xuan, Caiyun Shamonki, Jaime M. Chung, Alice DiNome, Maggie L. Chung, Maureen Sieling, Peter A. Lee, Delphine J. PLoS One Research Article Breast cancer affects one in eight women in their lifetime. Though diet, age and genetic predisposition are established risk factors, the majority of breast cancers have unknown etiology. The human microbiota refers to the collection of microbes inhabiting the human body. Imbalance in microbial communities, or microbial dysbiosis, has been implicated in various human diseases including obesity, diabetes, and colon cancer. Therefore, we investigated the potential role of microbiota in breast cancer by next-generation sequencing using breast tumor tissue and paired normal adjacent tissue from the same patient. In a qualitative survey of the breast microbiota DNA, we found that the bacterium Methylobacterium radiotolerans is relatively enriched in tumor tissue, while the bacterium Sphingomonas yanoikuyae is relatively enriched in paired normal tissue. The relative abundances of these two bacterial species were inversely correlated in paired normal breast tissue but not in tumor tissue, indicating that dysbiosis is associated with breast cancer. Furthermore, the total bacterial DNA load was reduced in tumor versus paired normal and healthy breast tissue as determined by quantitative PCR. Interestingly, bacterial DNA load correlated inversely with advanced disease, a finding that could have broad implications in diagnosis and staging of breast cancer. Lastly, we observed lower basal levels of antibacterial response gene expression in tumor versus healthy breast tissue. Taken together, these data indicate that microbial DNA is present in the breast and that bacteria or their components may influence the local immune microenvironment. Our findings suggest a previously unrecognized link between dysbiosis and breast cancer which has potential diagnostic and therapeutic implications. Public Library of Science 2014-01-08 /pmc/articles/PMC3885448/ /pubmed/24421902 http://dx.doi.org/10.1371/journal.pone.0083744 Text en © 2014 Xuan et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Xuan, Caiyun
Shamonki, Jaime M.
Chung, Alice
DiNome, Maggie L.
Chung, Maureen
Sieling, Peter A.
Lee, Delphine J.
Microbial Dysbiosis Is Associated with Human Breast Cancer
title Microbial Dysbiosis Is Associated with Human Breast Cancer
title_full Microbial Dysbiosis Is Associated with Human Breast Cancer
title_fullStr Microbial Dysbiosis Is Associated with Human Breast Cancer
title_full_unstemmed Microbial Dysbiosis Is Associated with Human Breast Cancer
title_short Microbial Dysbiosis Is Associated with Human Breast Cancer
title_sort microbial dysbiosis is associated with human breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3885448/
https://www.ncbi.nlm.nih.gov/pubmed/24421902
http://dx.doi.org/10.1371/journal.pone.0083744
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