Evidence map›Paper›PMID 41493538›Full record

ArticleDiscover oncology2026

Association of oral microbiota and digestive system cancers revealed by bidirectional two sample Mendelian randomization.

Ya-Jun Zhang, Qian-Yu Tian, Cai-E Wang, Shu-Xun Wei

Abstract read
In one paragraph

Article in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ya-Jun ZhangDepartment of Pharmacy, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, 24 Jinghua Road, Jianxi District, Luoyang, 471003, China. zhangyajun@haust.edu.cn.
Qian-Yu TianDepartment of Pharmacy, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, 24 Jinghua Road, Jianxi District, Luoyang, 471003, China.
Cai-E WangDepartment of Pharmacy, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, 24 Jinghua Road, Jianxi District, Luoyang, 471003, China.
Shu-Xun WeiDepartment of Vascular Surgery, Eastern Hepatobiliary Surgery Hospital, Naval Medical University/Second Military Medical University, 225 Changhai Road, Yangpu District, Shanghai, 200438, China. weishuxun126@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGrowing evidence suggests that there is a link between the oral microbiota and the development of digestive system cancers (DSCs). Nonetheless, the causal relationship between the oral microbiota and DSCs has yet to be established.

methodsTo evaluate the causal relationship between oral microbiota and DSCs, we employed Genome-wide association study (GWAS) summary statistics for both oral microbiota and DSCs, in conjunction with bidirectional two-sample Mendelian randomization (MR) analysis. Single nucleotide polymorphisms, which were free from confounding factors, were used as instrumental variables to infer causation. Sensitivity analyses were conducted to assess the robustness of our findings. This study employed datasets encompassing a wide range of cancer cases and controls, with an emphasis on Asian populations.

resultsOur analysis of 116 oral microbiota (65 from tongue dorsum and 51 from saliva) uncovered intricate causal associations with seven types of DSCs. We discovered that the genus TM7x (OR > 1, adjusted p < 0.05) poses a risk for hepatic bile duct cancer, and the genus Leptotrichia (OR = 6.38, 95%CI = 1.84-22.10, adjusted p < 0.05) poses a risk for pancreatic cancer. Furthermore, reverse MR analysis showed that DSCs influence the relative abundance of certain oral microbiota strains.

conclusionOur MR analysis has confirmed that there is a causal association between the oral microbiota and DSCs. This finding offers potential for creating novel microbial markers and treatments that modify the microbiota specifically for DSC patients.

Indexed as

CausalityDigestive system cancersMendelian randomizationOral microbiotaSNPs

Identifiers

PMID41493538
PMCPMC12868531

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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.