The gut microbiota: a key modulator of radiotherapy efficacy and toxicity in colorectal cancer

The gut microbiota plays a critical role in modulating both the efficacy and toxicity of radiotherapy in patients with colorectal cancer (CRC). This review synthesizes current evidence on the bidirectional interaction between the gut microbiome and radiotherapy, highlighting the mechanisms through which microbial communities influence radiosensitivity and treatment-related adverse effects. Specific microbiota-derived metabolites, such as short-chain fatty acids and methylglyoxal, can enhance the radiotherapeutic response by exacerbating DNA damage, promoting immunogenic cell death, and activating antitumor immunity. Conversely, dysbiosis may contribute to radioresistance and exacerbate radiation-induced enteritis by impairing intestinal barrier function and amplifying inflammatory responses. Therapeutic strategies targeting the gut microbiome—including probiotics, prebiotics, antibiotics, and fecal microbiota transplantation—show promise in improving radiotherapy outcomes and mitigating toxicity. However, its clinical application remains limited by issues of safety, variability in individual microbiome composition, and lack of standardized protocols. Further high-quality clinical trials are essential to validate these interventions and advance personalized microbial modulation approaches in CRC radiotherapy.

Authors

Institutions

Publication Details

Journal
Journal of Translational Medicine
Published
2026-08-27
DOI
https://doi.org/10.1186/s12967-026-08633-w
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
article

The gut microbiota: a key modulator of radiotherapy efficacy and toxicity in colorectal cancer

方鍾鉉, Shengzhe Ma, Xiaoyu He, Guanyu Yu et al.
Journal of Translational Medicine
Gut microbiota and health
article

The gut microbiota: a key modulator of radiotherapy efficacy and toxicity in colorectal cancer

方鍾鉉, Shengzhe Ma, Xiaoyu He, Guanyu Yu, Wei Zhang, Yue Yu, Yue Zhang, Ning Wang, Yanyong Yang
article en

Abstract

The gut microbiota plays a critical role in modulating both the efficacy and toxicity of radiotherapy in patients with colorectal cancer (CRC). This review synthesizes current evidence on the bidirectional interaction between the gut microbiome and radiotherapy, highlighting the mechanisms through which microbial communities influence radiosensitivity and treatment-related adverse effects. Specific microbiota-derived metabolites, such as short-chain fatty acids and methylglyoxal, can enhance the radiotherapeutic response by exacerbating DNA damage, promoting immunogenic cell death, and activating antitumor immunity. Conversely, dysbiosis may contribute to radioresistance and exacerbate radiation-induced enteritis by impairing intestinal barrier function and amplifying inflammatory responses. Therapeutic strategies targeting the gut microbiome—including probiotics, prebiotics, antibiotics, and fecal microbiota transplantation—show promise in improving radiotherapy outcomes and mitigating toxicity. However, its clinical application remains limited by issues of safety, variability in individual microbiome composition, and lack of standardized protocols. Further high-quality clinical trials are essential to validate these interventions and advance personalized microbial modulation approaches in CRC radiotherapy.

Journal of Translational Medicine
Naval University of Engineering (CN)
Good health and well-being
Openalex Percentile: Top 17%
Gut microbiota and health
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.