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Co-occurrence of driver and passenger bacteria in human colorectal cancer
BACKGROUND: Both genetic and epigenetic alterations have been reported to act as driving forces of tumorigenesis in colorectal cancer (CRC), but a growing body of evidence suggests that intestinal microbiota may be an aetiological factor in the initiation and progression of CRC. Recently, the “drive...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080773/ https://www.ncbi.nlm.nih.gov/pubmed/24995042 http://dx.doi.org/10.1186/1757-4749-6-26 |
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author | Geng, Jiawei Song, Qingfang Tang, Xiaodan Liang, Xiao Fan, Hong Peng, Hailing Guo, Qiang Zhang, Zhigang |
author_facet | Geng, Jiawei Song, Qingfang Tang, Xiaodan Liang, Xiao Fan, Hong Peng, Hailing Guo, Qiang Zhang, Zhigang |
author_sort | Geng, Jiawei |
collection | PubMed |
description | BACKGROUND: Both genetic and epigenetic alterations have been reported to act as driving forces of tumorigenesis in colorectal cancer (CRC), but a growing body of evidence suggests that intestinal microbiota may be an aetiological factor in the initiation and progression of CRC. Recently, the “driver-passenger” model for CRC has connected these different factors, but little has been done to characterize the CRC gut microbiome. FINDINGS: Building on the driver-passenger model, we used 454 pyrosequencing of bacterial 16S rRNA genes associated with 10 normal, 10 adenoma, and 8 tumor biopsy samples, and found 7 potential driver bacterial genera and 12 potential passenger bacterial genera (7 being pro-inflammatory and 5 anti-inflammatory). Further analysis also showed certain co-expression patterns among different clusters of bacteria that may potentially be related to the promotion or progression of gut cancers. CONCLUSIONS: The present findings provide preliminary experimental evidence supporting the proposition of bacterial “driver-passenger model” for CRC, and identified potentially novel microbial agents that may be connected to risk of CRC in a Han Chinese population. |
format | Online Article Text |
id | pubmed-4080773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40807732014-07-03 Co-occurrence of driver and passenger bacteria in human colorectal cancer Geng, Jiawei Song, Qingfang Tang, Xiaodan Liang, Xiao Fan, Hong Peng, Hailing Guo, Qiang Zhang, Zhigang Gut Pathog Short Report BACKGROUND: Both genetic and epigenetic alterations have been reported to act as driving forces of tumorigenesis in colorectal cancer (CRC), but a growing body of evidence suggests that intestinal microbiota may be an aetiological factor in the initiation and progression of CRC. Recently, the “driver-passenger” model for CRC has connected these different factors, but little has been done to characterize the CRC gut microbiome. FINDINGS: Building on the driver-passenger model, we used 454 pyrosequencing of bacterial 16S rRNA genes associated with 10 normal, 10 adenoma, and 8 tumor biopsy samples, and found 7 potential driver bacterial genera and 12 potential passenger bacterial genera (7 being pro-inflammatory and 5 anti-inflammatory). Further analysis also showed certain co-expression patterns among different clusters of bacteria that may potentially be related to the promotion or progression of gut cancers. CONCLUSIONS: The present findings provide preliminary experimental evidence supporting the proposition of bacterial “driver-passenger model” for CRC, and identified potentially novel microbial agents that may be connected to risk of CRC in a Han Chinese population. BioMed Central 2014-06-25 /pmc/articles/PMC4080773/ /pubmed/24995042 http://dx.doi.org/10.1186/1757-4749-6-26 Text en Copyright © 2014 Geng et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Short Report Geng, Jiawei Song, Qingfang Tang, Xiaodan Liang, Xiao Fan, Hong Peng, Hailing Guo, Qiang Zhang, Zhigang Co-occurrence of driver and passenger bacteria in human colorectal cancer |
title | Co-occurrence of driver and passenger bacteria in human colorectal cancer |
title_full | Co-occurrence of driver and passenger bacteria in human colorectal cancer |
title_fullStr | Co-occurrence of driver and passenger bacteria in human colorectal cancer |
title_full_unstemmed | Co-occurrence of driver and passenger bacteria in human colorectal cancer |
title_short | Co-occurrence of driver and passenger bacteria in human colorectal cancer |
title_sort | co-occurrence of driver and passenger bacteria in human colorectal cancer |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080773/ https://www.ncbi.nlm.nih.gov/pubmed/24995042 http://dx.doi.org/10.1186/1757-4749-6-26 |
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