Evidence map›Paper›PMID 39575247›Full record

ArticleFrontiers in immunology2024

Succession of the multi-site microbiome along pancreatic ductal adenocarcinoma tumorigenesis.

Yiqing Zhu, Xiao Liang, Mengfan Zhi, Lixiang Li, Guoming Zhang, Changxu Chen, Limei Wang, Peng Wang, Ning Zhong, Qiang Feng and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Axitinib plus Avelumab in Recurrent/Metastatic Adenoid Cystic Carcinoma: Biomarker Analysis and Updated Results of the Phase II Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
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  10. Neutrophil Killing ofJournal of innate immunity · 2026
    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

11 authors.

Yiqing Zhu *Department of Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Xiao Liang *Department of Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Mengfan Zhi *Shandong Key Laboratory of Oral Tissue Regeneration, Department of Human Microbiome, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.
Lixiang LiDepartment of Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Guoming ZhangDepartment of Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Changxu ChenDepartment of Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Limei WangDepartment of Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Peng WangDepartment of Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Ning ZhongDepartment of Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China.
Qiang FengShandong Key Laboratory of Oral Tissue Regeneration, Department of Human Microbiome, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.
Zhen LiDepartment of Gastroenterology, Qilu Hospital of Shandong University, Jinan, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: To investigate microbial characteristics across multibody sites from chronic pancreatitis (CP), through pancreatic benign tumors, to pancreatic ductal adenocarcinoma (PDAC) at different stages. Methods: 16S ribosomal RNA (rRNA) amplicon sequencing was conducted on saliva, duodenal fluid, and pancreatic tissue obtained via endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) of patients with CP, pancreatic benign tumors, PDAC in stage I/II, III, and IV. The neutral community model (NCM) assessed the microbial assembly contribution and MaAslin2 identified the differential microbes. Results: From CP to stage IV PDAC patients, there was a marked surge in influence of salivary and duodenal microbiota on constitution of pancreatic microbial communities. Our observations revealed a successive alteration in microbial species across various bodily sites during PDAC tumorigenesis. Notably, Conclusions: Salivary and duodenal microorganisms were prominent factors in shaping pancreatic microbial landscape in PDAC context. Further exploration of these microbial entities is imperative to unravel their specific roles in PDAC pathogenesis, potentially yielding insights for future therapeutic strategies.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsAdultAgedBacteriaCarcinogenesisFemaleHumansMaleMicrobiotaMiddle AgedPancreatitis, ChronicRNA, Ribosomal, 16SSalivaRNA, Ribosomal, 16Sendoscopic ultrasound-guided fine needle aspirationmicrobiotapancreatic neoplasmspancreatitistime series analysis

Identifiers

PMID39575247
PMCPMC11580624

What OpenQuestion holds

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Registered trials

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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.