Evidence map›Paper›PMID 40190311›Full record

ArticleArchives of medical science : AMS2025

Causal associations between blood metabolites and breast cancer.

Guanying Liang, Dazhuang Miao, Chun Du

Abstract read
In one paragraph

Article in Archives of medical science : AMS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

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3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Guanying LiangDepartment of Pathology, Affiliated Cancer Hospital of Harbin Medical University, Nangang, Harbin, Heilongjiang, China.
Dazhuang MiaoDepartment of Colorectal Cancer Surgery, Affiliated Cancer Hospital of Harbin Medical University, Nangang, Harbin, Heilongjiang, China.
Chun DuDepartment of Pathology, Affiliated Cancer Hospital of Harbin Medical University, Nangang, Harbin, Heilongjiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The associations between blood metabolites and breast cancer remain unclear. We conducted a systematic two-sample Mendelian randomization (MR) analysis to identify key human blood metabolites and potential biomarkers for breast cancer development. Material and methods: The data were extracted from large-scale genome-wide association study (GWAS) public databases. Instrumental variables were selected from a cohort study of 453 metabolic profiles from 7,824 participants. Breast cancer incidence data were obtained from a large cohort study involving 138,389 cases and 240,341 controls. Causal associations between human blood metabolites and breast cancer incidence were assessed using inverse-variance weighting, and MR-Egger regression. Results: Five human blood metabolites were identified as biomarkers for breast cancer: serine (OR = 2.25; 95% CI: 1.18-4.27), 10-undecenoate (11:1n1) (OR = 1.38; 95% CI: 1.00-1.90), X-12696 (OR = 2.15; 95% CI: 1.14-4.08), X-14626 (OR = 1.68; 95% CI: 1.15-2.46), and succinyl carnitine (OR = 1.58; 95% CI: 1.06-2.34). The sensitivity analysis results indicate no pleiotropy between the metabolites and breast cancer risk, confirming the robustness of the findings. Conclusions: This study in metabolomics research identified five human blood metabolites - serine, 10-undecenoate (11:1n1), X-12696, X-14626, and succinylcarnitine - as potential biomarkers for assessing breast cancer risk. Among these metabolites, serine and X-12696 showed the strongest associations with the likelihood of developing breast cancer.

Indexed as

breast cancerMendelian randomizationmetabolites

Identifiers

PMID40190311
PMCPMC11969560

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