Evidence map›Paper›PMID 41113652›Full record

ArticleFrontiers in microbiology2025

Stage-specific fecal and salivary microbiota signatures for noninvasive detection of colorectal cancer.

Zhenzhen Wu, Zhenzheng Zhu, Chenxi Zhou, Zhenyi Lin, Hujia Yang, Guanjun Jiang, Shuning Ding, Jieru Yu, Leitao Sun

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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

9 authors.

Zhenzhen Wu *Department of Medical Oncology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, Zhejiang, China.
Zhenzheng Zhu *Department of Medical Oncology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, Zhejiang, China.
Chenxi Zhou *Department of Medical Oncology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, Zhejiang, China.
Zhenyi LinDepartment of Medical Oncology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, Zhejiang, China.
Hujia YangDepartment of Medical Oncology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, Zhejiang, China.
Guanjun JiangLongyou Branch of Zhejiang Provincial Hospital of Chinese Medicine, Quzhou, Zhejiang, China.
Shuning DingCollege of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Jieru YuCollege of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, Zhejiang, China.
Leitao SunDepartment of Medical Oncology, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Fecal and salivary microbiota dysbiosis play a crucial role in the pathogenesis of colorectal cancer (CRC). We investigated whether the fecal and salivary microbiota were altered during colorectal tumorigenesis and evaluated their diagnostic performance. Methods: We enrolled 30 metastatic CRC patients, 30 nonmetastatic CRC patients, and 30 healthy controls between October 2023 and September 2024. Fecal and salivary samples were collected for microbial profiling via 16S rDNA sequencing and bioinformatics analysis. Results: Fecal and salivary microbiota composition differed during CRC progression, with salivary microbiota progressively enriched in the gut. In addition, fecal and salivary microbial co-occurrence networks dynamically altered during CRC progression. The natural connectivity of fecal microbial community networks exhibited decreased stability, whereas salivary microbial community networks showed increased stability as CRC progressed. Finally, specific fecal microbial amplicon sequence variants (ASVs) associated with colorectal carcinogenesis enabled precise stage-specific diagnosis of CRC, outperforming salivary ASVs classifiers. Conclusion: This study elucidates stage-specific microbial dynamics in CRC, providing novel insights into clinical diagnostic strategies.

Indexed as

16S rDNA gene sequencingcolorectal cancerfecal microbiotamicrobial co-occurrence networkssalivary microbiota

Identifiers

PMID41113652
PMCPMC12531261

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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.