Aphthous stomatitis - computational biology suggests external biotic stimulus and immunogenic cell death involved.


Journal

BMC oral health
ISSN: 1472-6831
Titre abrégé: BMC Oral Health
Pays: England
ID NLM: 101088684

Informations de publication

Date de publication:
29 Sep 2024
Historique:
received: 06 01 2024
accepted: 16 09 2024
medline: 30 9 2024
pubmed: 30 9 2024
entrez: 29 9 2024
Statut: epublish

Résumé

The exact cause of recurrent aphthous stomatitis is still unknown, making it a challenge to develop effective treatments. This study employs computational biology to investigate the molecular basis of recurrent aphthous stomatitis, aiming to identify the nature of the stimuli triggering these ulcers and the type of cell death involved. To understand the molecular underpinnings of recurrent aphthous stomatitis, we used the Génie tool for gene identification, targeting those associated with cell death in recurrent aphthous stomatitis. The ToppGene Suite was employed for functional enrichment analysis. We also used Reactome and InteractiVenn for protein integration and prioritization against a PANoptosis gene list, enabling the construction of a protein-protein interaction network to pinpoint key proteins in recurrent aphthous stomatitis pathogenesis. The study's computational approach identified 1,375 protein-coding genes linked to recurrent aphthous stomatitis. Critical among these were proteins responsive to bacterial stimuli, especially high mobility group protein B1 (HMGB1), toll-like receptor 2 (TLR2), and toll-like receptor 4 (TLR4). The enrichment analysis suggested an external biotic factor, likely bacterial, as a triggering agent in recurrent aphthous stomatitis. The protein interaction network highlighted the roles of tumor necrosis factor (TNF), NF-kappa-B essential modulator (IKBKG), and tumor necrosis factor receptor superfamily member 1A (TNFRSF1A), indicating an immunogenic cell death mechanism, potentially PANoptosis, in recurrent aphthous stomatitis. The findings propose that bacterial stimuli could trigger recurrent aphthous stomatitis through a PANoptosis-related cell death pathway. This new understanding of recurrent aphthous stomatitis pathogenesis underscores the significance of oral microbiota in the condition. Future experimental validation and therapeutic strategy development based on these findings are necessary.

Sections du résumé

BACKGROUND BACKGROUND
The exact cause of recurrent aphthous stomatitis is still unknown, making it a challenge to develop effective treatments. This study employs computational biology to investigate the molecular basis of recurrent aphthous stomatitis, aiming to identify the nature of the stimuli triggering these ulcers and the type of cell death involved.
METHODS METHODS
To understand the molecular underpinnings of recurrent aphthous stomatitis, we used the Génie tool for gene identification, targeting those associated with cell death in recurrent aphthous stomatitis. The ToppGene Suite was employed for functional enrichment analysis. We also used Reactome and InteractiVenn for protein integration and prioritization against a PANoptosis gene list, enabling the construction of a protein-protein interaction network to pinpoint key proteins in recurrent aphthous stomatitis pathogenesis.
RESULTS RESULTS
The study's computational approach identified 1,375 protein-coding genes linked to recurrent aphthous stomatitis. Critical among these were proteins responsive to bacterial stimuli, especially high mobility group protein B1 (HMGB1), toll-like receptor 2 (TLR2), and toll-like receptor 4 (TLR4). The enrichment analysis suggested an external biotic factor, likely bacterial, as a triggering agent in recurrent aphthous stomatitis. The protein interaction network highlighted the roles of tumor necrosis factor (TNF), NF-kappa-B essential modulator (IKBKG), and tumor necrosis factor receptor superfamily member 1A (TNFRSF1A), indicating an immunogenic cell death mechanism, potentially PANoptosis, in recurrent aphthous stomatitis.
CONCLUSION CONCLUSIONS
The findings propose that bacterial stimuli could trigger recurrent aphthous stomatitis through a PANoptosis-related cell death pathway. This new understanding of recurrent aphthous stomatitis pathogenesis underscores the significance of oral microbiota in the condition. Future experimental validation and therapeutic strategy development based on these findings are necessary.

Identifiants

pubmed: 39343890
doi: 10.1186/s12903-024-04917-z
pii: 10.1186/s12903-024-04917-z
doi:

Substances chimiques

HMGB1 Protein 0
Toll-Like Receptor 2 0
Toll-Like Receptor 4 0
TLR4 protein, human 0
TLR2 protein, human 0
HMGB1 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1154

Informations de copyright

© 2024. The Author(s).

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Auteurs

Ignacio Riveros-Gomez (I)

Laboratorio de Histopatología Oral y Maxilofacial, Unidad de Medicina Oral y Patología Oral, Departamento de Estomatología, Facultad de Odontología, Universidad de Talca, Avenida Lircay S/N, Campus Norte Universidad de Talca, Edificio de Ciencias Biomédicas, Oficina N°4, Talca, 3460000, Región del Maule, Chile.

Joaquin Vasquez-Marin (J)

Laboratorio de Histopatología Oral y Maxilofacial, Unidad de Medicina Oral y Patología Oral, Departamento de Estomatología, Facultad de Odontología, Universidad de Talca, Avenida Lircay S/N, Campus Norte Universidad de Talca, Edificio de Ciencias Biomédicas, Oficina N°4, Talca, 3460000, Región del Maule, Chile.

Elisa Ximena Huerta-Garcia (EX)

Laboratorio de Histopatología Oral y Maxilofacial, Unidad de Medicina Oral y Patología Oral, Departamento de Estomatología, Facultad de Odontología, Universidad de Talca, Avenida Lircay S/N, Campus Norte Universidad de Talca, Edificio de Ciencias Biomédicas, Oficina N°4, Talca, 3460000, Región del Maule, Chile.

Paola Andrea Camargo-Ayala (PA)

Laboratorio de Histopatología Oral y Maxilofacial, Unidad de Medicina Oral y Patología Oral, Departamento de Estomatología, Facultad de Odontología, Universidad de Talca, Avenida Lircay S/N, Campus Norte Universidad de Talca, Edificio de Ciencias Biomédicas, Oficina N°4, Talca, 3460000, Región del Maule, Chile.

Cesar Rivera (C)

Laboratorio de Histopatología Oral y Maxilofacial, Unidad de Medicina Oral y Patología Oral, Departamento de Estomatología, Facultad de Odontología, Universidad de Talca, Avenida Lircay S/N, Campus Norte Universidad de Talca, Edificio de Ciencias Biomédicas, Oficina N°4, Talca, 3460000, Región del Maule, Chile. cerivera@utalca.cl.

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