Evidence map›Paper›PMID 33690612›Full record

ArticlePloS one2021

Characterization of biliary microbiota dysbiosis in extrahepatic cholangiocarcinoma.

Massa Saab, Denis Mestivier, Masoudreza Sohrabi, Christophe Rodriguez, Mahmood Reza Khonsari, Amirhossein Faraji, Iradj Sobhani

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 2 pooled it
10.2field-weighted citation impact, top 1% of its field
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

56 citing papers in PubMed, 2 syntheses or guidelines pooled it, 70 citations in OpenAlex.

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  8. Microbial dysbiosis in cholangiocarcinoma.Frontiers in microbiology · 2026
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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

7 authors at 3 institutions in 2 countries.

Massa SaabEarly Detection of Colon Cancer Using Molecular and Microbial Markers (EC2M3)-EA 7375 Team, University Paris-Est Creteil (UPEC), Créteil, France.ORCID 0000-0001-5786-2056
Denis MestivierEarly Detection of Colon Cancer Using Molecular and Microbial Markers (EC2M3)-EA 7375 Team, University Paris-Est Creteil (UPEC), Créteil, France.
Masoudreza SohrabiGastroIntestinal and Liver Diseases Research Center (GILDRC), Iran University of Medical Sciences and Firouzgar hospital (Prof. F. Zamani), Tehran, Iran.
Christophe RodriguezBioinformatic Core Facility, IMRB UMR 955 - INSERM, UPEC, Créteil Cedex, France.
Mahmood Reza KhonsariGastroIntestinal and Liver Diseases Research Center (GILDRC), Iran University of Medical Sciences and Firouzgar hospital (Prof. F. Zamani), Tehran, Iran.
Amirhossein FarajiGastroIntestinal and Liver Diseases Research Center (GILDRC), Iran University of Medical Sciences and Firouzgar hospital (Prof. F. Zamani), Tehran, Iran.
Iradj SobhaniEarly Detection of Colon Cancer Using Molecular and Microbial Markers (EC2M3)-EA 7375 Team, University Paris-Est Creteil (UPEC), Créteil, France.
Inserm · FRIran University of Medical Sciences · IRUniversité Paris-Est Créteil · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extrahepatic cholangiocarcinoma (CCA) accounts for 3% of digestive cancers. The role of biliary microbiota as an environment-related modulator has been scarcely investigated in CCA, and the putative impact of associated diseases has not been yet assessed. We characterized the biliary microbiota in CCA patients in order to identify a specific CCA-related dysbiosis. The biliary effluents were collected through an endoscopic retrograde pancreatic cholangiography (ERCP) examination involving 28 CCA and 47 patients with gallstones, herein considered as controls. The biliary effluents were submitted to bacterial DNA extraction and 16S rRNA sequencing, using Illumina technology. Overall, 32% of CCA and 22% of controls displayed another associated disease, such as diabetes, pancreatitis, inflammatory bowel disease, or primary sclerosing cholangitis. Such associated diseases were considered in the comparisons that were made. Principal coordinate analysis (PCoA) detected a significant disparity of biliary microbiota composition between CCA patients and controls without an associated disease. Amongst the most abundant phyla, Proteobacteria did not significantly differ between CCA patients and controls, whereas Firmicutes levels were lower and Bacteroidetes higher in CCAs' biliary microbiota than in the controls' microbiota. The most abundant genera were Enterococcus, Streptococcus, Bacteroides, Klebsiella, and Pyramidobacter in CCA's biliary microbiota. Additionally, levels of Bacteroides, Geobacillus, Meiothermus, and Anoxybacillus genera were significantly higher in CCA patients' biliary microbiota, without an associated disease, in comparison with controls. A specific CCA-related dysbiosis was identified as compared to controls independently from associated diseases. This suggests that a microorganism community may be involved in CCA pathogenesis.

Indexed as

MicrobiotaAdultAgedBacillotaBacteroidetesBileBile Duct NeoplasmsCholangiocarcinomaDysbiosisFemaleGallstonesHumansMaleMiddle AgedProteobacteria

Identifiers

PMID33690612
PMCPMC7943025
OpenAlexW3133955278

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.