Evidence map›Paper›PMID 40113766›Full record

ArticleScientific data2025

Oral microbiome and mycobiome dynamics in cancer therapy-induced oral mucositis.

Laurentia Nodit, Joseph R Kelley, Timothy J Panella, Antje Bruckbauer, Paul G Nodit, Grace A Shope, Kellie Peyton, Dawn M Klingeman, Russell Zaretzki, Alyssa Carrell and 1 more

Abstract readDataset
In one paragraph

Article in Scientific data, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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.

Laurentia NoditUniversity of Tennessee Graduate School of Medicine Knoxville, Department of Pathology and Biorepository, Knoxville, TN, USA. lnodit@utmck.edu.
Joseph R KelleyUniversity of Tennessee Graduate School of Medicine Knoxville, Department of Radiation Oncology, Knoxville, TN, USA.
Timothy J PanellaUniversity of Tennessee Graduate School of Medicine Knoxville, University Cancer Specialists, Knoxville, TN, USA.
Antje BruckbauerUniversity of Tennessee Graduate School of Medicine Knoxville, Department of Pathology and Biorepository, Knoxville, TN, USA.
Paul G NoditUniversity of Tennessee Health Science Canter, Graduate School of Medicine, Memphis, TN, USA.
Grace A ShopeUniversity of Tennessee Graduate School of Medicine Knoxville, Department of Radiation Oncology, Knoxville, TN, USA.
Kellie PeytonOak Ridge National Laboratory, Biosciences Division, Oak Ridge, TN, USA.
Dawn M KlingemanOak Ridge National Laboratory, Biosciences Division, Oak Ridge, TN, USA.ORCID http://orcid.org/0000-0002-4307-2560
Russell ZaretzkiUniversity of Tennessee Business Analytics and Statistics, Knoxville, TN, USA.
Alyssa CarrellOak Ridge National Laboratory, Biosciences Division, Oak Ridge, TN, USA.
Mircea PodarOak Ridge National Laboratory, Biosciences Division, Oak Ridge, TN, USA. podarm@ornl.gov.ORCID http://orcid.org/0000-0003-2776-0205

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer therapy-induced oral mucositis is a frequent major oncological problem, secondary to cytotoxicity of chemo-radiation treatment. Oral mucositis commonly occurs 7-10 days after initiation of therapy; it is a dose-limiting side effect causing significant pain, eating difficulty, need for parenteral nutrition and a rise of infections. The pathobiology derives from complex interactions between the epithelial component, inflammation, and the oral microbiome. Our longitudinal study analysed the dynamics of the oral microbiome (bacteria and fungi) in nineteen patients undergoing chemo-radiation therapy for oral and oropharyngeal squamous cell carcinoma as compared to healthy volunteers. The microbiome was characterized in multiple oral sample types using rRNA and ITS sequence amplicons and followed the treatment regimens. Microbial taxonomic diversity and relative abundance may be correlated with disease state, type of treatment and responses. Identification of microbial-host interactions could lead to further therapeutic interventions of mucositis to re-establish normal flora and promote patients' health. Data presented here could enhance, complement and diversify other studies that link microbiomes to oral disease, prophylactics, treatments, and outcome.

Indexed as

MicrobiotaMouthMycobiomeStomatitisBacteriaHumansLongitudinal Studies

Identifiers

PMID40113766
PMCPMC11926371

What Socratic 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 Socratic graph.