Oral-Gut-Estrobolome Axis May Exert a Selective Impact on Oral Cancer.

estrogens human microbiota inflammation mouth neoplasms oral medicine oral pathology

Journal

Journal of dental research
ISSN: 1544-0591
Titre abrégé: J Dent Res
Pays: United States
ID NLM: 0354343

Informations de publication

Date de publication:
07 Apr 2024
Historique:
medline: 8 4 2024
pubmed: 8 4 2024
entrez: 7 4 2024
Statut: aheadofprint

Résumé

A subset of bacterial species that holds genes encoding for β-glucuronidase and β-galactosidase, enzymes involved in the metabolism of conjugated estrogens, is called the "estrobolome." There is an emerging interest embracing this concept, as it may exert a selective impact on a number of pathologies, including oral cancer. Although the estrobolome bacteria are typically part of the gut microbiota, recent experimental pieces of evidence have suggested a crosstalk among oral and gut microbiota. In fact, several oral bacterial species are well represented also in the gut microbiota, and these microbes can effectively induce the estrobolome activation. The main pathways used for activating the estrobolome are based on the induction of the expression patterns for 2 bacterial enzymes: β-glucuronidase and aromatase, both involved in the increase of estrogen released in the bloodstream and consequently in the salivary compartment. Mechanistically, high estrogen availability in saliva is responsible for an increase in oral cancer risk for different reasons: briefly, 1) estrogens directly exert biological and metabolic effects on oral mucosa cells; 2) they can modulate the pathological profile of some bacteria, somewhere associated with neoplastic processes (i.e.,

Identifiants

pubmed: 38584298
doi: 10.1177/00220345241236125
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

220345241236125

Déclaration de conflit d'intérêts

Declaration of Conflicting InterestsThe authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

M Tatullo (M)

Department of Translational Biomedicine and Neuroscience, University of Bari "Aldo Moro," Bari, Italy.
School of Dentistry, University of Dundee, Dundee, Scotland, UK.

J Nor (J)

Department of Cariology, Restorative Sciences, and Endodontics, University of Michigan School of Dentistry, Ann Arbor, MI, USA.
Department of Otolaryngology-Head & Neck Surgery, University of Michigan School of Medicine, Ann Arbor, MI, USA.
Department of Biomedical Engineering, University of Michigan College of Engineering, Ann Arbor, MI, USA.
University of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.

G Orrù (G)

Department of Surgical Sciences, Oral Biotechnology Laboratory (OBL), University of Cagliari, Cagliari, Italy.

A Piattelli (A)

School of Dentistry, Saint Camillus International University for Health Sciences, Rome, Italy.

E Cascardi (E)

Department of Precision and Regenerative Medicine and Ionian Area (DiMePRe-J), University of Bari Aldo Moro, Bari, Puglia, Italy.

G Spagnuolo (G)

Department of Neurosciences, Reproductive and Odontostomatological Sciences, University of Naples "Federico II" Naples, Italy.

Classifications MeSH