# Interplay Between Gut Microbiota and Cholesterol Metabolism in Colorectal Cancer

**Authors:** Sarah Wing Lam Li, Oscar Ting Hei Au, Effie Yin Tung Lau, Riley Yanjun Lu, Adrian Leonard Zaleski, Jessie Qiaoyi Liang

PMC · DOI: 10.3390/ijms27062553 · International Journal of Molecular Sciences · 2026-03-10

## TL;DR

This review explores how gut bacteria and cholesterol metabolism interact to influence colorectal cancer development and suggests new treatment strategies.

## Contribution

The paper introduces a novel perspective on the bidirectional relationship between gut microbiota and cholesterol metabolism in CRC.

## Key findings

- Gut microbial species can increase CRC risk by modulating cholesterol metabolism through bile acids and oxysterols.
- Disrupted cholesterol metabolism can worsen microbial dysbiosis and promote CRC.
- Targeting gut microbiota and cholesterol metabolism offers potential for CRC prevention and treatment.

## Abstract

Both gut microbiota dysbiosis and disrupted cholesterol metabolism are associated with colorectal cancer (CRC). While the interactions between these two factors have been well explored in diseases such as cardiovascular disease and atherosclerosis, their interactions and underlying mechanisms in CRC pathogenesis remain insufficiently explored, constituting a critical area for further investigation. This review examines the complex relationship between gut microbiota and cholesterol metabolism in CRC development from 2 perspectives: how specific gut microbial species can increase CRC risk by modulating cholesterol metabolism, particularly through bile acids and oxysterols, and how disrupted cholesterol metabolism can exacerbate microbial dysbiosis and promote CRC. The bidirectional relationship between gut dysbiosis and cholesterol dysregulation creates a vicious cycle that drives CRC development. Moreover, the potential of targeting the gut microbiome and cholesterol metabolism to develop new strategies for preventing and treating CRC is discussed, highlighting the promise of certain bacterial strains that exert protective effects via cholesterol-lowering mechanisms. By elucidating the intricate connections between gut microbiota, cholesterol metabolism, and CRC, this review paves the way for innovative approaches in CRC prevention and therapy.

## Linked entities

- **Diseases:** colorectal cancer (MONDO:0005575), CRC (MONDO:0005575)

## Full-text entities

- **Diseases:** CRC (MESH:D015179), atherosclerosis (MESH:D050197), dysbiosis (MESH:D064806), cardiovascular disease (MESH:D002318)
- **Chemicals:** bile acids (MESH:D001647), oxysterols (MESH:D000072376), Cholesterol (MESH:D002784)
- **Species:** gut metagenome (species) [taxon 749906]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13026627/full.md

## References

131 references — full list in the complete paper: https://tomesphere.com/paper/PMC13026627/full.md

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Source: https://tomesphere.com/paper/PMC13026627