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pmid:34422640

Global Analysis of Microbiota Signatures in Four Major Types of Gastrointestinal Cancer.

Jihan Wang · Yangyang Wang · Zhenzhen Li · Xiaoguang Gao · Dageng Huang

Frontiers in oncology · 2021 doi:10.3389/fonc.2021.685641

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:34422640
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science-record
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2026-11-01T15:41:48Z
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title
Global Analysis of Microbiota Signatures in Four Major Types of Gastrointestinal Cancer.
doi
10.3389/fonc.2021.685641
pmid
34422640
authors array · 5 items
[0]
Jihan Wang
[1]
Yangyang Wang
[2]
Zhenzhen Li
[3]
Xiaoguang Gao
[4]
Dageng Huang
journal
Frontiers in oncology
year
2021
abstract
The gut microbiota has been previously linked with tumorigenesis and gastrointestinal cancer progression; however, intra-tumor microbiota analysis has just emerged and deserves increasing attention. Based on the public databases of The Cancer Microbiome Atlas (TCMA) and The Cancer Genome Atlas (TCGA), this study identified the tissue/organ microbial signatures generated from 443 biosamples of four major gastrointestinal cancer types, including esophageal carcinoma (ESCA), which further includes esophageal adenocarcinoma (EAD) and esophageal squamous cell carcinoma (ESCC), stomach adenocarcinoma (STAD), colon adenocarcinoma (COAD), and rectum adenocarcinoma (READ). According to partial least squares discrimination analysis (PLS-DA), the profile differences in microbial communities between the tumor and normal samples were not particularly noticeable across the four cancer cohorts, whereas paired comparison analyses revealed several specific differences in bacteria between tumor and normal samples in the EAD, STAD, and COAD samples. The taxa classified from the phylum to genus level revealed a trend of distinguishable microbial profiles between upper and lower gastrointestinal tumors. The Bacteroidetes/Firmicutes ratio in lower gastrointestinal tract tumors was nearly three times that in upper gastrointestinal tract tumors. We also determined the relative tissue/organ-prevalent microbes for each of the four cohorts at the order and genus levels. Microbe Alistipes, Blautia, Pasteurellales, and Porphyromonas compositions were correlated with the clinical characteristics of patients with gastrointestinal cancer, particularly colorectal cancer. Taken together, our findings indicate that microbial profiles shift across different gastrointestinal cancer types and that microbial colonization is highly site-specific. Composition of specific microbes can be indicative of cancer stage or disease progression. Overall, this study indicates that the microbial community and abundance in human tissues can be determined using publicly available data, and provides a new perspective for intra-tissue/organ microbiota research.
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The Kaplan–Meier model from the survival and survminer packages in R version 4.0.2 was used for survival analysis based on microbial abundance.
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The Kaplan–Meier model from the survival and survminer packages in R version 4.0.2 was used for survival analysis based on microbial abundance.
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sections[13] "Data Availability Statement" paragraph 2
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The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding authors.
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Clinical characteristics of the four types of gastrointestinal tumors in this study (derived from The Cancer Microbiome Atlas and The Cancer Genome Atlas databases).
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Data Acquisition From TCMA and TCGA
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Clinical characteristics of the four types of gastrointestinal tumors in this study (derived from The Cancer Microbiome Atlas and The Cancer Genome Atlas databases).
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STAD
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READ
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39 (86.67)
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10 (22.22)
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26 (65.00)
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[6]
47 (37.60)
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[8]
17 (37.78)
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[2]
9 (22.50)
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[4]
33 (25.98)
[5]
[6]
35 (28.00)
[7]
[8]
12 (26.67)
[9]
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Stage IV
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18 (14.17)
[5]
[6]
14 (11.20)
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[8]
6 (13.33)
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The Kaplan–Meier model from the survival and survminer packages in R version 4.0.2 was used for survival analysis based on microbial abundance.
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Based on the public databases of The Cancer Microbiome Atlas (TCMA) and The Cancer Genome Atlas (TCGA), this study identified the tissue/organ microbial signatures generated from 443 biosamples of four major gastrointestinal cancer types, including esophageal carcinoma (ESCA), which further includes esophageal adenocarcinoma (EAD) and esophageal squamous cell carcinoma (ESCC), stomach adenocarcinoma (STAD), colon adenocarcinoma (COAD), and rectum adenocarcinoma (READ). According to partial least squares discrimination analysis (PLS-DA), the profile differences in microbial communities between the tumor and normal samples were not particularly noticeable across the four cancer cohorts, whereas paired comparison analyses revealed several specific differences in bacteria between tumor and normal samples in the EAD, STAD, and COAD samples. The taxa classified from the phylum to genus level revealed a trend of distinguishable microbial profiles between upper and lower gastrointestinal tumors. The Bacteroidetes/Firmicutes ratio in lower gastrointestinal tract tumors was nearly three times that in upper gastrointestinal tract tumors. We also determined the relative tissue/organ-prevalent microbes for each of the four cohorts at the order and genus levels. Microbe Alistipes, Blautia, Pasteurellales, and Porphyromonas compositions were correlated with the clinical characteristics of patients with gastrointestinal cancer, particularly colorectal cancer. Taken together, our findings indicate that microbial profiles shift across different gastrointestinal cancer types and that microbial colonization is highly site-specific. Composition of specific microbes can be indicative of cancer stage or disease progression. 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