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Colorectal Cancer-Associated Microbiome Patterns and Signatures
Lan Zhao1,2, William C Cho3, Mark R Nicolls1,2
1Department of Medicine, Stanford University School of Medicine, Stanford, CA, United States.
Frontiers in Genetics
|January 10, 2022
Summary
This study reveals consistent gut microbiome changes in colorectal cancer (CRC) patients across multiple cohorts. Specific microbial depletion and enrichment, including oral pathogens, are identified as key CRC-associated dysbiosis signatures.
Area of Science:
- Microbiology
- Oncology
- Genomics
Background:
- Gut microbiota plays a crucial role in health and disease.
- Gut dysbiosis is linked to colorectal cancer (CRC) risk and progression.
- Understanding CRC-associated microbial changes is vital for diagnosis and treatment.
Purpose of the Study:
- To identify and characterize CRC-associated gut dysbiosis across independent cohorts.
- To explore microbe-microbe interactions and host-microbe networks in CRC.
- To investigate reproducible microbial signatures and their link to CRC heterogeneity.
Main Methods:
- Analysis of six independent CRC cohorts with matched normal tissues.
- Comparison of microbial community composition between cancerous and normal tissues.
- Identification of microbial interaction networks and patient-microbe patterns using biclustering.
Main Results:
- Consistent depletion of commensal microbes (e.g., Clostridia, Bacteroidia) and enrichment of oral pathogens (e.g., Fusobacterium nucleatum) in CRC tumors.
- Identification of two reproducible patient-microbe interaction patterns (P0 and P1) across cohorts.
- P1 patients showed reduced microbial diversity and higher levels of oral pathogens compared to controls and P0.
Conclusions:
- Reproducible microbial signatures characterize colorectal cancer across diverse populations.
- CRC heterogeneity is partly explained by variations in microbial composition and host interactions.
- These findings offer insights into CRC pathogenesis and potential diagnostic biomarkers.
Keywords:
biclusteringcolorectal cancerdysbiosisgut microbiomeoral-related pathogenspatient-microbe interactions
