Dysbiosis of human gut microbiome in young-onset colorectal cancer
Open accessAbstract
The incidence of sporadic young-onset colorectal cancer (yCRC) is increasing. A significant knowledge gap exists in the gut microbiota and its diagnostic value for yCRC patients. Through 16S rRNA gene sequencing, 728 samples are collected to identify microbial markers, and an independent cohort of 310 samples is used to validate the results. Furthermore, species-level and functional analysis are performed by metagenome sequencing using 200 samples. Gut microbial diversity is increased in yCRC. Flavonifractor plautii is an important bacterial species in yCRC, while genus Streptococcus contains the key phylotype in the old-onset colorectal cancer. Functional analysis reveals that yCRC has unique characteristics of bacterial metabolism characterized by the dominance of DNA binding and RNA-dependent DNA biosynthetic process. The random forest classifier model achieves a powerful classification potential. This study highlights the potential of the gut microbiota biomarkers as a promising non-invasive tool for the accurate detection and distinction of individuals with yCRC.
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Compared with patients aged 50 years or older, those with early onset CRC usually present with more advanced disease and have different pathological features and CRC GOMS.
“Compared with patients of ≥50 years of age, those with early onset CRC usually present with more advanced disease, and have different pathological features and CRC GOMS83,84.”
From Gut OncoMicrobiome Signatures (GOMS) as next-generation biomarkers for cancer immunotherapy (2023) · cites this paper as [83]
Early onset CRC GOMS is characterized by enrichment of F. plautii and increased metabolism of tryptophan, bile acids, and choline.
“The latter is characterized by an enrichment of F. plautii and increased metabolism of tryptophan, bile acids and choline.”
From Gut OncoMicrobiome Signatures (GOMS) as next-generation biomarkers for cancer immunotherapy (2023) · cites this paper as [83]
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- Authors
- Yang, Y., Du, L., Shi, D., Kong, C., Liu, J., Liu, G., Li, X., & Ma, Y.
- Affiliations
- Shanghai Medical College of Fudan University (CN)
- Second Hospital of Shandong University (CN)
- Tongji University (CN)
- Fudan University Shanghai Cancer Center (CN)
- Corresponding author
- Ma, Yanlei
- Venue
- Nature Communications
- Published
- 2021-11-19
- Volume
- 12
- Issue
- 1
- Pages
- 6757-6757
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC8604900
- OpenAlex
- W3213755739
- Cited by
- 303
- References
- 65
- Citations by year
- 2026: 60 · 2025: 64 · 2024: 95 · 2023: 53 · 2022: 29 · 2017: 1 · 2016: 1
- FWCI
- 14.21
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Natural Science Foundation of China (Nos. 81920108026, 81871964, 81802412)
- Shanghai Science and Technology Development Foundation (No.19410713300)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
- Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
- Keywords
- early-onset colorectal cancer, gut dysbiosis, microbial biomarkers, Flavonifractor plautii, Streptococcus, gut microbiota diversity, bacterial metabolism, DNA binding, non-invasive cancer detection, random forest classification
- MeSH terms
- Clostridiales, Eubacteriales, Gastrointestinal Microbiome, Adult, Aged, Feces, Female, Humans, Male, Middle Aged, Streptococcus, Colorectal Neoplasms, Case-Control Studies, Age of Onset, Healthy Volunteers, Dysbiosis
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