Evidence map›Paper›PMID 40788433›Full record

ArticleDiscover oncology2025

Gut microbiota and breast cancer risk: a Mendelian randomization study stratified by ER status.

Jian Yue, Lei Gu, Sheng Chen, Fang Wen, Guoxing Huang

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jian Yue *Department of Breast Surgery, Gaozhou People's Hospital, No.89 Xiguan Road, 525200, Gaozhou, China.
Lei Gu *Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Sheng ChenDepartment of Breast Surgery, Gaozhou People's Hospital, No.89 Xiguan Road, 525200, Gaozhou, China.
Fang WenDepartment of Obstetrics and Gynecology, The Affiliated Hospital of Guizhou Medical University, No. 28 Guiyi Street, Yunyan District, Guiyang, 550000, China. wfzcloud@outlook.com.
Guoxing HuangDepartment of Breast Surgery, Gaozhou People's Hospital, No.89 Xiguan Road, 525200, Gaozhou, China. huangguoxing0668@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe potential causal relationship between gut microbiota (GM) and breast cancer (BC), particularly its estrogen receptor (ER)-positive (ER+) and ER-negative (ER-) subtypes, remains insufficiently characterized.

methodWe conducted a two-sample Mendelian randomization (MR) analysis to examine genetically predicted causal associations between 473 GM features (abundance in stool) and BC, including overall BC (Ncase = 24,270, Ncontrol = 222,078), ER+ BC (Ncase = 14,540, Ncontrol = 221,705) and ER- BC (Ncase = 9,724, Ncontrol = 221,705).

resultThe MR results demonstrated differential causal associations between GM and BC subtypes: For overall BC risk, lower Barnesiella abundance (OR = 0.93; 95%CI 0.88-0.98; P = 0.006) was protective, whereas higher Providencia abundance (OR = 1.30; 95%CI 1.11-1.51; P = 0.0008) increased risk. Among ER+ BC cases, five GM showed significant associations: Dokdonella (OR = 1.38; 95%CI 1.12-1.70; P = 0.0024), Flavonifractor sp900199495 (OR = 0.81; 95%CI 0.69-0.94; P = 0.0054), Rhodanobacter (OR = 1.45; 95%CI 1.10-1.92; P = 0.0087), Ruminococcus (OR = 0.73; 95%CI 0.58-0.92; P = 0.0080), and UBA7177 sp002491225 (OR = 1.33; 95%CI 1.08-1.63; P = 0.0067). In ER- BC, seven GM factors exhibited causal relationships: Bacteroides A plebeius (OR = 0.90; 95%CI 0.84-0.97; P = 0.0077), CAG-273 sp003507395 (OR = 0.89; 95%CI 0.82-0.95; P = 0.0009), CAG-390 sp003523225 (OR = 0.82; 95%CI 0.71-0.95; P = 0.0064), CAG-433 (OR = 0.86; 95%CI 0.78-0.95; P = 0.0030), Chromobacteriaceae (OR = 0.57; 95%CI 0.39-0.83; P = 0.0034), Providencia (OR = 1.48; 95%CI 1.18-1.86; P = 0.0007), and Syntrophorhabdaceae (OR = 1.52; 95%CI 1.14-2.04; P = 0.0050).

conclusionsOur genetically informed MR analysis provides suggestive evidence for the differential causal roles of specific GM in overall, ER + and ER- BC pathogenesis, offering potential biomarkers for therapeutic intervention strategies.

Indexed as

Breast cancerEstrogen receptorGut microbiotaMendelian randomization

Identifiers

PMID40788433
PMCPMC12339805

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.