Cargando…

Study of the Relationship between Microbiome and Colorectal Cancer Susceptibility Using 16SrRNA Sequencing

A lot of previous studies have recently reported that the gut microbiota influences the development of colorectal cancer (CRC) in Western countries, but the role of the gut microbiota in Chinese population must be investigated fully. The goal of this study was to determine the role of the gut microb...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Wanxin, Zhang, Ren, Shu, Rong, Yu, Jinjing, Li, Huan, Long, Hui, Jin, Shu, Li, Shengbao, Hu, Qiuyu, Yao, Fei, Zhou, Chuanren, Huang, Qiyou, Hu, Xiafen, Chen, Meng, Hu, Weiguo, Wang, Qiang, Fang, Shenying, Wu, Qingming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011317/
https://www.ncbi.nlm.nih.gov/pubmed/32083132
http://dx.doi.org/10.1155/2020/7828392
_version_ 1783496043478908928
author Liu, Wanxin
Zhang, Ren
Shu, Rong
Yu, Jinjing
Li, Huan
Long, Hui
Jin, Shu
Li, Shengbao
Hu, Qiuyu
Yao, Fei
Zhou, Chuanren
Huang, Qiyou
Hu, Xiafen
Chen, Meng
Hu, Weiguo
Wang, Qiang
Fang, Shenying
Wu, Qingming
author_facet Liu, Wanxin
Zhang, Ren
Shu, Rong
Yu, Jinjing
Li, Huan
Long, Hui
Jin, Shu
Li, Shengbao
Hu, Qiuyu
Yao, Fei
Zhou, Chuanren
Huang, Qiyou
Hu, Xiafen
Chen, Meng
Hu, Weiguo
Wang, Qiang
Fang, Shenying
Wu, Qingming
author_sort Liu, Wanxin
collection PubMed
description A lot of previous studies have recently reported that the gut microbiota influences the development of colorectal cancer (CRC) in Western countries, but the role of the gut microbiota in Chinese population must be investigated fully. The goal of this study was to determine the role of the gut microbiome in the initiation and development of CRC. We collected fecal samples of 206 Chinese individuals: 59 with polyp (group P), 54 with adenoma (group A), 51 with colorectal cancer (group CC), and 42 healthy controls (group HC).16S ribosomal RNA (rRNA) was used to compare the microbiota community structures among healthy controls, patients with polyp, and those with adenoma or colorectal cancer. Our study proved that intestinal flora, as a specific indicator, showed significant differences in its diversity and composition. Sobs, Chao, and Ace indexes of group CC were significantly lower than those of the healthy control group (CC group: Sobs, Chao, and Ace indexes were 217.3 ± 69, 4265.1 ± 80.7, and 268.6 ± 78.1, respectively; HC group: Sobs, Chao, and Ace indexes were 228.8 ± 44.4, 272.9 ± 58.6, and 271.9 ± 57.2, respectively). When compared with the healthy individuals, the species richness and diversity of intestinal flora in patients with colorectal cancer were significantly reduced: PCA and PCoA both revealed that a significant separation in bacterial community composition between the CC group and HC group (with PCA using the first two principal component scores of PC1 14.73% and PC2 10.34% of the explained variance, respectively; PCoA : PC1 = 14%, PC2 = 9%, PC3 = 6%). Wilcox tests was used to analyze differences between the two groups, it reveals that Firmicutes (P=0.000356), Fusobacteria (P=0.000001), Proteobacteria (P=0.000796), Spirochaetes (P=0.013421), Synergistetes (P=0.005642) were phyla with significantly different distributions between cases and controls. The proportion of microorganism composition is varying at different stages of colon cancer development: Bacteroidetes (52.14%) and Firmicutes (35.88%) were enriched in the healthy individuals; on the phylum level, the abundance of Bacteroidetes (52.14%-53.92%-52.46%–47.06%) and Firmicutes (35.88%-29.73%-24.27%–25.36%) is decreasing with the development of health-polyp-adenomas-CRC, and the abundance of Proteobacteria (9.33%-12.31%-16.51%–22.37%) is increasing. PCA and PCOA analysis showed there was no significant (P < 0.05) difference in species similarity between precancerous and carcinogenic states. However, the composition of the microflora in patients with precancerous lesions (including patients with adenoma and polyp) was proved to have no significant disparity (P < 0.05). Our study provides insights into new angles to dig out potential biomarkers in diagnosis and treatment of colorectal cancer and to provide scientific advice for a healthy lifestyle for the sake of gut microbiota.
format Online
Article
Text
id pubmed-7011317
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Hindawi
record_format MEDLINE/PubMed
spelling pubmed-70113172020-02-20 Study of the Relationship between Microbiome and Colorectal Cancer Susceptibility Using 16SrRNA Sequencing Liu, Wanxin Zhang, Ren Shu, Rong Yu, Jinjing Li, Huan Long, Hui Jin, Shu Li, Shengbao Hu, Qiuyu Yao, Fei Zhou, Chuanren Huang, Qiyou Hu, Xiafen Chen, Meng Hu, Weiguo Wang, Qiang Fang, Shenying Wu, Qingming Biomed Res Int Research Article A lot of previous studies have recently reported that the gut microbiota influences the development of colorectal cancer (CRC) in Western countries, but the role of the gut microbiota in Chinese population must be investigated fully. The goal of this study was to determine the role of the gut microbiome in the initiation and development of CRC. We collected fecal samples of 206 Chinese individuals: 59 with polyp (group P), 54 with adenoma (group A), 51 with colorectal cancer (group CC), and 42 healthy controls (group HC).16S ribosomal RNA (rRNA) was used to compare the microbiota community structures among healthy controls, patients with polyp, and those with adenoma or colorectal cancer. Our study proved that intestinal flora, as a specific indicator, showed significant differences in its diversity and composition. Sobs, Chao, and Ace indexes of group CC were significantly lower than those of the healthy control group (CC group: Sobs, Chao, and Ace indexes were 217.3 ± 69, 4265.1 ± 80.7, and 268.6 ± 78.1, respectively; HC group: Sobs, Chao, and Ace indexes were 228.8 ± 44.4, 272.9 ± 58.6, and 271.9 ± 57.2, respectively). When compared with the healthy individuals, the species richness and diversity of intestinal flora in patients with colorectal cancer were significantly reduced: PCA and PCoA both revealed that a significant separation in bacterial community composition between the CC group and HC group (with PCA using the first two principal component scores of PC1 14.73% and PC2 10.34% of the explained variance, respectively; PCoA : PC1 = 14%, PC2 = 9%, PC3 = 6%). Wilcox tests was used to analyze differences between the two groups, it reveals that Firmicutes (P=0.000356), Fusobacteria (P=0.000001), Proteobacteria (P=0.000796), Spirochaetes (P=0.013421), Synergistetes (P=0.005642) were phyla with significantly different distributions between cases and controls. The proportion of microorganism composition is varying at different stages of colon cancer development: Bacteroidetes (52.14%) and Firmicutes (35.88%) were enriched in the healthy individuals; on the phylum level, the abundance of Bacteroidetes (52.14%-53.92%-52.46%–47.06%) and Firmicutes (35.88%-29.73%-24.27%–25.36%) is decreasing with the development of health-polyp-adenomas-CRC, and the abundance of Proteobacteria (9.33%-12.31%-16.51%–22.37%) is increasing. PCA and PCOA analysis showed there was no significant (P < 0.05) difference in species similarity between precancerous and carcinogenic states. However, the composition of the microflora in patients with precancerous lesions (including patients with adenoma and polyp) was proved to have no significant disparity (P < 0.05). Our study provides insights into new angles to dig out potential biomarkers in diagnosis and treatment of colorectal cancer and to provide scientific advice for a healthy lifestyle for the sake of gut microbiota. Hindawi 2020-01-30 /pmc/articles/PMC7011317/ /pubmed/32083132 http://dx.doi.org/10.1155/2020/7828392 Text en Copyright © 2020 Wanxin Liu et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Liu, Wanxin
Zhang, Ren
Shu, Rong
Yu, Jinjing
Li, Huan
Long, Hui
Jin, Shu
Li, Shengbao
Hu, Qiuyu
Yao, Fei
Zhou, Chuanren
Huang, Qiyou
Hu, Xiafen
Chen, Meng
Hu, Weiguo
Wang, Qiang
Fang, Shenying
Wu, Qingming
Study of the Relationship between Microbiome and Colorectal Cancer Susceptibility Using 16SrRNA Sequencing
title Study of the Relationship between Microbiome and Colorectal Cancer Susceptibility Using 16SrRNA Sequencing
title_full Study of the Relationship between Microbiome and Colorectal Cancer Susceptibility Using 16SrRNA Sequencing
title_fullStr Study of the Relationship between Microbiome and Colorectal Cancer Susceptibility Using 16SrRNA Sequencing
title_full_unstemmed Study of the Relationship between Microbiome and Colorectal Cancer Susceptibility Using 16SrRNA Sequencing
title_short Study of the Relationship between Microbiome and Colorectal Cancer Susceptibility Using 16SrRNA Sequencing
title_sort study of the relationship between microbiome and colorectal cancer susceptibility using 16srrna sequencing
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011317/
https://www.ncbi.nlm.nih.gov/pubmed/32083132
http://dx.doi.org/10.1155/2020/7828392
work_keys_str_mv AT liuwanxin studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT zhangren studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT shurong studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT yujinjing studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT lihuan studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT longhui studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT jinshu studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT lishengbao studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT huqiuyu studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT yaofei studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT zhouchuanren studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT huangqiyou studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT huxiafen studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT chenmeng studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT huweiguo studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT wangqiang studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT fangshenying studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing
AT wuqingming studyoftherelationshipbetweenmicrobiomeandcolorectalcancersusceptibilityusing16srrnasequencing