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Updated: Jul 1, 2026

Genome-Wide Analysis of DNA Methylation in Gastrointestinal Cancer
Published on: September 18, 2020
Metaproteomics characterizes human gut microbiome function in colorectal cancer
Shuping Long1,2,3, Yi Yang1, Chengpin Shen4
1Department of Chemistry, Shanghai Stomatological Hospital, Fudan University, Shanghai, China.
Colorectal cancer (CRC) pathogenesis involves gut microbiome changes. Metaproteomics reveals altered microbial protein functions, particularly iron transport and oxidative stress responses, in CRC patients, offering new diagnostic insights.
Area of Science:
- Microbiology
- Gastroenterology
- Proteomics
Background:
- Colorectal cancer (CRC) pathogenesis is linked to gut microbiome alterations.
- Previous research focused on microbial taxonomic changes, leaving functional variations largely unexplored.
Purpose of the Study:
- To investigate functional differences in the gut microbiome of CRC patients versus healthy individuals using quantitative metaproteomics.
- To identify specific microbial protein alterations associated with CRC.
Main Methods:
- Quantitative metaproteomic analysis of fecal samples from CRC patients and healthy volunteers.
- Identification and quantification of microbial peptides and protein groups.
- Statistical analysis to determine significant differences in protein abundance.
Main Results:
- Identified 91,902 peptides, 30,062 microbial protein groups, and 195 microbial genera.
- 341 microbial proteins showed significantly different abundance between CRC patients and controls.
- Altered proteins were associated with iron metabolism, oxidative stress, and DNA repair, linked to high local iron and oxidative stress in CRC patients' colons.
Conclusions:
- Metaproteomics provides valuable functional insights into the gut microflora relevant to CRC pathogenesis.
- Identified functional microbial shifts may aid in future clinical diagnosis of colorectal cancer.
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