Evidence map›Paper›PMID 39420333›Full record

ArticleJournal of translational medicine2024

Parvimonas micra forms a distinct bacterial network with oral pathobionts in colorectal cancer patients.

Thyra Löwenmark, Linda Köhn, Therese Kellgren, William Rosenbaum, Vicky Bronnec, Anna Löfgren-Burström, Carl Zingmark, Pär Larsson, Michael Dahlberg, Bjoern O Schroeder and 4 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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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

14 authors.

Thyra LöwenmarkDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.
Linda KöhnDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.
Therese KellgrenDepartment of Mathematics and Mathematical Statistics, Umeå University, Umeå, Sweden.
William RosenbaumDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.
Vicky BronnecDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.
Anna Löfgren-BurströmDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.
Carl ZingmarkDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.
Pär LarssonDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.
Michael DahlbergDepartment of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
Bjoern O SchroederDepartment of Molecular Biology, Umeå University, Umeå, Sweden.
Sun Nyunt WaiDepartment of Molecular Biology, Umeå University, Umeå, Sweden.
Ingrid LjuslinderDepartment of Diagnostics and Intervention, Umeå University, Umeå, Sweden.
Sofia EdinDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden.
Richard PalmqvistDepartment of Medical Biosciences, Pathology, Umeå University, Umeå, Sweden. richard.palmqvist@umu.se.ORCID 0000-0002-9933-2843

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMounting evidence suggests a significant role of the gut microbiota in the development and progression of colorectal cancer (CRC). In particular, an over-representation of oral pathogens has been linked to CRC. The aim of this study was to further investigate the faecal microbial landscape of CRC patients, with a focus on the oral pathogens Parvimonas micra and Fusobacterium nucleatum.

methodsIn this study, 16S rRNA sequencing was conducted using faecal samples from CRC patients (n = 275) and controls without pathological findings (n = 95).

resultsWe discovered a significant difference in microbial composition depending on tumour location and microsatellite instability (MSI) status, with P. micra, F. nucleatum, and Peptostreptococcus stomatis found to be more abundant in patients with MSI tumours. Moreover, P. micra and F. nucleatum were associated with a cluster of CRC-related bacteria including Bacteroides fragilis as well as with other oral pathogens such as P. stomatis and various Porphyromonas species. This cluster was distinctly different in the control group, suggesting its potential linkage with CRC.

conclusionsOur results suggest a similar distribution of several CRC-associated bacteria within CRC patients, underscoring the importance of considering the concomitant presence of bacterial species in studies investigating the mechanisms of CRC development and progression.

Indexed as

Colorectal NeoplasmsAdultAgedBacillotaBacteriaCase-Control StudiesFecesFemaleFusobacterium nucleatumHumansMaleMicrosatellite InstabilityMiddle AgedMouthRNA, Ribosomal, 16SRNA, Ribosomal, 16SColorectal cancerFusobacterium nucelatumIntestinal microbiotaOral pathobiontsParvimonas micra

Identifiers

PMID39420333
PMCPMC11487773

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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.