Evidence map›Paper›PMID 37627304›Full record

ArticleBiomolecules2023

Assessment of Oxidative Stress-Induced Oral Epithelial Toxicity.

Ali I Mohammed, Simran Sangha, Huynh Nguyen, Dong Ha Shin, Michelle Pan, Hayoung Park, Michael J McCullough, Antonio Celentano, Nicola Cirillo

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  8. Review
  9. Article
  10. Article
  11. Nanotherapies Based on ROS Regulation in Oral Diseases.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  12. Unraveling the complexity of radiotherapy- and chemotherapy-induced oral mucositis: insights into pathogenesis and intervention strategies.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
    Review
  13. Article
  14. 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

9 authors at 2 institutions in 3 countries.

Ali I MohammedMelbourne Dental School, The University of Melbourne, Carlton, VIC 3053, Australia.ORCID 0000-0003-0017-5233
Simran SanghaMelbourne Dental School, The University of Melbourne, Carlton, VIC 3053, Australia.
Huynh NguyenMelbourne Dental School, The University of Melbourne, Carlton, VIC 3053, Australia.ORCID 0000-0002-4033-7519
Dong Ha ShinMelbourne Dental School, The University of Melbourne, Carlton, VIC 3053, Australia.
Michelle PanMelbourne Dental School, The University of Melbourne, Carlton, VIC 3053, Australia.
Hayoung ParkMelbourne Dental School, The University of Melbourne, Carlton, VIC 3053, Australia.
Michael J McCulloughMelbourne Dental School, The University of Melbourne, Carlton, VIC 3053, Australia.ORCID 0000-0001-7829-4684
Antonio CelentanoMelbourne Dental School, The University of Melbourne, Carlton, VIC 3053, Australia.ORCID 0000-0003-4293-2511
Nicola CirilloMelbourne Dental School, The University of Melbourne, Carlton, VIC 3053, Australia.ORCID 0000-0003-1429-1323
The University of Melbourne · AUUniversity of Jordan · JO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reactive oxygen species (ROS) are highly reactive molecules generated in living organisms and an excessive production of ROS culminates in oxidative stress and cellular damage. Notably, oxidative stress plays a critical role in the pathogenesis of a number of oral mucosal diseases, including oral mucositis, which remains one of cancer treatments' most common side effects. We have shown previously that oral keratinocytes are remarkably sensitive to oxidative stress, and this may hinder the development and reproducibility of epithelial cell-based models of oral disease. Here, we examined the oxidative stress signatures that parallel oral toxicity by reproducing the initial events taking place during cancer treatment-induced oral mucositis. We used three oral epithelial cell lines (an immortalized normal human oral keratinocyte cell line, OKF6, and malignant oral keratinocytes, H357 and H400), as well as a mouse model of mucositis. The cells were subjected to increasing oxidative stress by incubation with hydrogen peroxide (H

Indexed as

Drug-Related Side Effects and Adverse ReactionsMucositisStomatitisAnimalsDisease Models, AnimalFluorescent DyesHumansHydrogen PeroxideMiceOxidative StressReactive Oxygen SpeciesReproducibility of ResultsFluorescent DyesHydrogen PeroxideReactive Oxygen Speciesepithelial injuryoral keratinocytesoxidative stressreactive oxygen species

Identifiers

PMID37627304
PMCPMC10452318
OpenAlexW4385758476

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.