Evidence map›Paper›PMID 41293165›Full record

ReviewFrontiers in immunology2025

Harnessing the gut microbiome to modulate ferroptosis: a metabolic strategy for the treatment of digestive tract cancers.

Jiexia Wen, Huagang Liang, Min Zhao, Bin Xuan, Xiangcai Meng, Yang Liu, Liwei Wang, Li He, Tao Zhou, Yang Tao and 1 more

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Jiexia WenDepartment of Central Laboratory, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Huagang LiangKey Laboratory of Research on Molecular Mechanism of Gastrointestinal Tumors in Qinhuangdao, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Min ZhaoKey Laboratory of Research on Molecular Mechanism of Gastrointestinal Tumors in Qinhuangdao, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Bin XuanKey Laboratory of Research on Molecular Mechanism of Gastrointestinal Tumors in Qinhuangdao, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Xiangcai MengKey Laboratory of Research on Molecular Mechanism of Gastrointestinal Tumors in Qinhuangdao, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Yang LiuKey Laboratory of Research on Molecular Mechanism of Gastrointestinal Tumors in Qinhuangdao, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Liwei WangKey Laboratory of Research on Molecular Mechanism of Gastrointestinal Tumors in Qinhuangdao, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Li HeKey Laboratory of Research on Molecular Mechanism of Gastrointestinal Tumors in Qinhuangdao, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Tao ZhouKey Laboratory of Research on Molecular Mechanism of Gastrointestinal Tumors in Qinhuangdao, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Yang TaoDepartment of Central Laboratory, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.
Yimin WangDepartment of Central Laboratory, The First Hospital of Qinhuangdao, Qinhuangdao, Hebei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ferroptosis is a form of regulated cell death defined in recent years, characterized by iron-dependent accumulation of lipid peroxides. A large body of research has demonstrated that ferroptosis is closely associated with the progression of gastrointestinal tumors (such as gastric cancer, colorectal cancer, and esophageal cancer), and gastrointestinal tumor cells exhibit unique sensitivity to ferroptosis. This indicates that ferroptosis has emerged as a highly promising strategy to combat therapy-resistant colorectal cancer. Although the intrinsic ferroptosis-suppressive and ferroptosis-promoting pathways in gastrointestinal tumors have been fully elucidated, the current understanding of the extrinsic metabolites and pathways that regulate ferroptosis in the pathogenesis of gastrointestinal tumors remains relatively limited. Emerging studies have shown a strong link between gut microbial metabolism and the progression of gastrointestinal tumors. This review summarizes the relevant aspects of gut microbiota metabolism, explores how these gut microbiota-derived metabolites regulate cancer progression through ferroptosis, and proposes that targeting gut microbiota-mediated ferroptosis represents a potential therapeutic approach for gastrointestinal tumors.

Indexed as

FerroptosisGastrointestinal MicrobiomeGastrointestinal NeoplasmsAnimalsHumanscancer therapydigestive tract tumorsferroptosisgut microbiota metabolitestumor microenvironment

Identifiers

PMID41293165
PMCPMC12641001

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.