Evidence map›Paper›PMID 35188867›Full record

ArticleGut microbes

Pro-mutagenic effects of the gut microbiota in a Lynch syndrome mouse model.

Wietske Pieters, Floor Hugenholtz, Kevin Kos, Maxime Cammeraat, Teddy C Moliej, Daphne Kaldenbach, Sjoerd Klarenbeek, Mark Davids, Lisa Drost, Charlotte de Konink and 3 more

Open access · goldAbstract read
In one paragraph

Article in Gut microbes. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Observational
  6. iScience · 2024
    Article
  7. Article
  8. Review
  9. Genetic heterogeneity of colorectal cancer and the microbiome.World journal of gastrointestinal oncology · 2023
    Review
  10. Article
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

13 authors at 1 institution in 1 country.

Wietske PietersDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0002-0375-5789
Floor HugenholtzMicrobiota Center Amsterdam, Amsterdam, The Netherlands.
Kevin KosDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0002-2407-4413
Maxime CammeraatDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Teddy C MoliejDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Daphne KaldenbachDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Sjoerd KlarenbeekExperimental Animal Pathology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0002-1891-1940
Mark DavidsMicrobiota Center Amsterdam, Amsterdam, The Netherlands.
Lisa DrostDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Charlotte de KoninkDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Elly Delzenne-GoetteDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Karin E de VisserDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0002-0293-868X
Hein Te RieleDivision of Tumor Biology and Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0003-0255-4042
The Netherlands Cancer Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gut microbiota strongly impacts the development of sporadic colorectal cancer (CRC), but it is largely unknown how the microbiota affects the pathogenesis of mismatch-repair-deficient CRC in the context of Lynch syndrome. In a mouse model for Lynch syndrome, we found a nearly complete loss of intestinal tumor development when animals were transferred from a conventional "open" animal facility to specific-pathogen-free (SPF) conditions. Using 16S sequencing we detected large changes in microbiota composition between the two facilities. Transcriptomic analyses of tumor-free intestinal tissues showed signs of strong intestinal inflammation in conventional mice. Whole exome sequencing of tumors developing in

Indexed as

Colorectal Neoplasms, Hereditary NonpolyposisGastrointestinal MicrobiomeAnimalsDisease Models, AnimalMiceMutagenesisMutagensMutS Homolog 2 ProteinMutagensMutS Homolog 2 Proteincolorectal cancerLynch syndromemicrobiotamismatch repairmutagenesis

Identifiers

PMID35188867
PMCPMC8865281
OpenAlexW4212938529

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.