Fecal microbial markers, particularly Fusobacterium nucleatum and Peptostreptococcus anaerobius, show potential for diagnosing CRC and monitoring its progression, with P. anaerobius exhibiting the highest diagnostic value when combined with Fn.
Key Findings
Results
Fusobacterium nucleatum (Fn) and Peptostreptococcus anaerobius (P. anaerobius) showed significant correlations with CRC stage and metastasis.
Both bacteria were identified as potential diagnostic biomarkers for CRC.
Correlations were observed with both disease stage and metastatic status.
Bacterial biomarkers were identified through fecal metagenomic sequencing datasets and validated using fluorescence quantitative PCR.
The study enrolled 180 participants: 65 healthy controls, 65 colorectal adenoma patients, and 50 CRC patients.
Results
P. anaerobius exhibited the highest diagnostic value among individual microbes when combined with Fn.
Among individual microbial markers examined, P. anaerobius had the highest diagnostic value.
The combination of P. anaerobius with Fn yielded superior diagnostic performance compared to individual markers alone.
Diagnostic value was assessed using comprehensive statistical methodologies.
Fecal samples were analyzed using fluorescence quantitative polymerase chain reaction to confirm biomarker relative abundance.
Results
Differentially abundant bacterial species were identified across healthy controls, adenoma, and CRC patient groups.
The study analyzed fecal microbial biomarkers associated with CRC progression across three distinct groups.
Groups included 65 healthy controls (HC), 65 colorectal adenoma patients, and 50 CRC patients.
An evolutionary model for CRC progression was established based on differential microbial abundance.
A treatment efficacy and prognostication model was also established from the microbial data.
Background
Gold standard diagnostic methods for CRC have limited sensitivity and specificity.
Current gold standard methods include invasive procedures and serum biomarkers.
These methods are characterized by limited sensitivity and specificity for CRC detection.
This limitation motivated the investigation of noninvasive fecal microbial biomarkers as an alternative approach.
The authors emphasize the need for precision screening tailored to high-risk cohorts to improve early detection and intervention strategies.
Conclusions
Fecal microbial markers were established as applicable for both diagnosing CRC and monitoring its progression.
The study culminated in the establishment of an evolutionary model for CRC progression.
A treatment efficacy and prognostication model supported by comprehensive statistical methodologies was established.
The approach used fecal metagenomic sequencing datasets to identify potential bacterial biomarkers, followed by validation using fluorescence quantitative PCR.
The findings underscore the potential application of fecal microbial markers, particularly Fn and P. anaerobius, for both diagnosis and progression monitoring.
Shen F, Xu C, Wang C. (2026). Gut Microbiome Diagnostic Biomarkers for Colorectal Cancer.. The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology. https://doi.org/10.5152/tjg.2025.24810