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Updated: Jan 28, 2026

Metagenomic Analysis of Silage
Published on: January 13, 2017
Compositional and Functional Differences between Microbiota and Cervical Carcinogenesis as Identified by Shotgun
Minji Kwon1, Sang-Soo Seo2, Mi Kyung Kim3
1Division of Cancer Epidemiology and Prevention, National Cancer Center, 323, Ilsan-ro, Ilsandong-gu, Goyang-si 10408, Korea. 74433@ncc.re.kr.
The cervical microbiome differs in composition and function between normal tissues and those with cervical intraepithelial neoplasia (CIN) or cancer. These microbiome changes are linked to altered metabolic pathways, suggesting a role in cervical carcinogenesis.
Area of Science:
- Microbiome research
- Cervical carcinogenesis
- Metagenomics
Background:
- Emerging evidence suggests a role for the microbiome in cervical disease.
- However, detailed understanding of microbiome composition and function in cervical carcinogenesis remains limited.
Purpose of the Study:
- To identify compositional and functional alterations of cervical microbiomes in Korean women with cervical carcinogenesis.
- To investigate differences in microbial abundances and metabolic functions between normal, pre-cancerous (cervical intraepithelial neoplasia 2/3), and cancerous cervical tissues.
Main Methods:
- Shotgun metagenomic sequencing was employed to analyze cervical metagenomes.
- Samples included 17 cases of cervical intraepithelial neoplasia 2/3, 12 cases of cervical cancer, and 18 normal controls.
- Microbial abundances and enriched metabolic functions (KEGG orthologies and COG categories) were identified.
Main Results:
- Distinct microbial genera were enriched in cervical cancer (Alkaliphilus, Pseudothermotoga, Wolbachia), CIN 2/3 (Lactobacillus, Staphylococcus, Candidatus Endolissoclinum), and normal controls (Pseudoalteromonas, Psychrobacter).
- Six KEGG orthologies involved in 10 pathways were associated with increased risk of CIN2/3 and cervical cancer.
- Peptidoglycan synthesis pathways were enriched, while dioxin degradation and 4-oxalocrotonate tautomerase pathways were depleted. The 'Defense mechanisms' COG category was depleted in cervical cancer.
Conclusions:
- Cervical microbiome composition and metagenomic profiles significantly differ between cervical lesions and normal subjects.
- These findings highlight potential microbial biomarkers and functional pathways involved in cervical carcinogenesis.
- Larger sample sizes and aggregated data are recommended for future studies to ensure statistical power and reproducibility.
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