Evidence map›Paper›PMID 35082322›Full record

ArticleScientific reports2022

Intestinal microbiota profiles in a genetic model of colon tumorigenesis correlates with colon cancer biomarkers.

Francesco Vitali, Katia Tortora, Monica Di Paola, Gianluca Bartolucci, Marta Menicatti, Carlotta De Filippo, Giovanna Caderni

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

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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 4 institutions in 1 country.

Francesco VitaliInstitute of Agricultural Biology and Biotechnology, National Research Council (CNR), Via Moruzzi, 1, 56124, Pisa, Italy.ORCID 0000-0001-9125-4337
Katia TortoraNEUROFARBA Department, Pharmacology and Toxicology Section, University of Florence, Viale Pieraccini 6, 50139, Florence, Italy.ORCID 0000-0002-0932-9983
Monica Di PaolaGastroenterology and Nutrition Unit, Meyer Children's Hospital, Florence, Italy.ORCID 0000-0002-2324-2649
Gianluca BartolucciNEUROFARBA Department, Pharmacology and Toxicology Section, University of Florence, Viale Pieraccini 6, 50139, Florence, Italy.ORCID 0000-0002-5631-8769
Marta MenicattiNEUROFARBA Department, Pharmacology and Toxicology Section, University of Florence, Viale Pieraccini 6, 50139, Florence, Italy.ORCID 0000-0001-8302-7644
Carlotta De FilippoInstitute of Agricultural Biology and Biotechnology, National Research Council (CNR), Via Moruzzi, 1, 56124, Pisa, Italy. carlotta.defilippo@ibba.cnr.it.ORCID 0000-0002-2222-6524
Giovanna CaderniNEUROFARBA Department, Pharmacology and Toxicology Section, University of Florence, Viale Pieraccini 6, 50139, Florence, Italy.ORCID 0000-0002-0039-4738
University of Florence · ITInstitute of Agricultural Biology and Biotechnology · ITMeyer Children's Hospital · ITNational Research Council · IT

Funding

Joint Programming Initiative A healthy diet for a healthy life Interrelation of the Intestinal Microbiome, Diet and Health (meaTic)
6 · The paper itself

Abstract

Faecal (FM) and colon mucosal associated microbiota (MAM) were studied in a model of colorectal cancer (CRC), the Apc-mutated Pirc rats, and in age-paired wt F344 rats. Principal Coordinates Analysis indicated that samples' distribution was driven by age, with samples of young rats (1 month old; without tumours) separated from older ones (11-month-old; bearing tumours). Diversity analysis showed significant differences between FM and MAM in older Pirc rats, and between MAM of both Pirc and wt rats and the tumour microbiota, enriched in Enterococcus, Escherichia/Shigella, Proteus and Bifidobacteriaceae. In young animals, Pirc FM was enriched in the genus Delftia, while wt FM was enriched in Lactobacillus and Streptococcus. Some CRC biomarkers and faecal short chain fatty acids (SCFAs) were also measured. Colon proliferation and DClK1 expression, a pro-survival mucosal marker, were higher in Pirc than in wt rats, while the mucin MUC2, was lower in Pirc rats. Branched SCFAs were higher in Pirc than in wt animals. By Spearman analysis CRC biomarkers correlated with FM (in both young and old rats) and with MAM (in young rats), suggesting a specific relationship between the gut microbiota profile and these functional mucosal parameters deserving further investigation.

Indexed as

Age FactorsAnimalsBifidobacteriumBiomarkers, TumorCarcinogenesisColonColonic NeoplasmsDisease Models, AnimalDoublecortin-Like KinasesEnterococcusEscherichiaFatty Acids, VolatileFecesGene Expression RegulationLactobacillusMaleBiomarkers, TumorDclk1 protein, ratDoublecortin-Like KinasesFatty Acids, VolatileMuc2 protein, ratMucin-2

Identifiers

PMID35082322
PMCPMC8792020
OpenAlexW4210768786

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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.