Evidence map›Paper›PMID 41298864›Full record

ArticleAMB Express2025

Integrative mendelian randomization and multi-omics analysis reveal a gut microbiota-metabolite-CXCL10 axis in breast cancer.

Junyuan Qu, Fangfang Zhang, Lifang Wang, Yong Zhang, Yuxiang Wang

Abstract read
In one paragraph

Article in AMB Express, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Junyuan Qu *Department of Breast Surgery, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, 030013, China.
Fangfang Zhang *Department of Ultrasound, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, 030013, China.
Lifang WangDepartment of General, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, 030013, China.
Yong ZhangDepartment of Ultrasound, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, 030013, China. zhang_yong_2018@126.com.
Yuxiang WangDepartment of Ultrasound, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, 030013, China. yuxiang_wangphd@126.com.

Funding

Doctoral Departure Fund of Shanxi Cancer Hospital Dr202303Shanxi Province High level Talent Introduction Project Dr202303
6 · The paper itself

Abstract

Breast cancer remains the leading cause of cancer morbidity and mortality worldwide, with limited efficacy in advanced breast cancer patients due to tumor heterogeneity and drug resistance. Emerging evidence suggests that the gut microbiota is associated with breast cancer progression through metabolites and immunomodulatory effects. However, mechanistic insights and therapeutic targets combining the gut microbiota and host genetics remain underexplored. In this study, we performed Mendelian randomization (MR) analysis via cis-eQTLs from breast cancer GWASs and druggable gene datasets to identify genes causally associated with breast cancer risk. Differential gene expression analysis was conducted using TCGA data. Gut microbiota-target-metabolite networks were constructed from the gutMGene database, and immunophenotyping was assessed via CIBERSORT. Molecular docking and molecular dynamics simulations were used to evaluate the interactions between gut microbiota metabolites and key targets. Magnetic resonance and transcriptome analyses revealed 14 candidate genes associated with breast cancer risk, of which CXCL10 was positively associated with disease progression (OR = 1.124, P = 0.007). CXCL10 expression was strongly correlated with the infiltration of CD4 + memory-activated T cells, CD4 + follicular helper T cells, CD8 + T cells, and gamma delta T cells. Network analysis revealed that Enterococcus faecalis was associated with the activation of CXCL10. Stable molecular dynamics simulations indicated that Lariciresinol was a high-affinity ligand for CXCL10. This comprehensive study highlights the role of the gut microbiota-metabolite-gene axis in breast cancer progression, particularly in Enterococcus faecalis-mediated CXCL10 activation. By modulating CXCL10, Lariciresinol has emerged as a promising candidate for targeted therapy. These findings suggest that the gut microbiota-metabolite-gene axis may play a regulatory role in breast cancer progression and propose Lariciresinol as a potential therapeutic candidate. However, given the computational foundation and in vitro validation, this study should be considered hypothesis-generating, and further in vivo and clinical investigations are warranted to confirm the proposed mechanisms.

Indexed as

Breast cancerCXCL10Gut microbiotaMendelian randomizationTherapeutic targets

Identifiers

PMID41298864
PMCPMC12748410

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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 OpenQuestion graph.