# Dysbiosis of oral and gut microbiomes characterized by elevated Lactococcus in a mouse model of oral squamous cell carcinoma

**Authors:** Euon Jung Tak, Beom-Jin Goo, Jae-Yun Lee, Jeong Eun Han, Yun-Seok Jeong, Hae-In Joe, Hojun Sung, Hyun Sik Kim, Jin-Woo Bae

PMC · DOI: 10.1038/s41522-026-00934-8 · 2026-02-13

## TL;DR

This study shows that the oral and gut microbiomes change during oral cancer development in mice, with Lactococcus bacteria increasing and possibly helping reduce inflammation.

## Contribution

The study identifies Lactococcus as a key microbial player in oral cancer progression and suggests potential protective effects.

## Key findings

- Lactococcus abundance increases in the oral microbiome during 4-NQO-induced oral cancer in mice.
- Oral administration of Lactococcus strains reduced inflammation in the mouse model.
- Lactococcus lysates showed protein-dependent cytotoxicity against oral cancer cells in vitro.

## Abstract

Oral microorganisms contribute to the progression of oral squamous cell carcinoma (OSCC), and the gut microbiome may also influence OSCC by modulating systemic immunity. This study investigated oral and gut microbial changes in a 4-nitroquinoline N-oxide (4-NQO)-induced OSCC mouse model. After 16 weeks of 4-NQO exposure, significant alterations were observed in the beta diversity of both oral and gut microbiomes. Notably, the relative abundance of Lactococcus increased, especially in oral microbiomes, from week 6 to 16, followed by a decline at week 22, suggesting a 4-NQO-induced niche favorable to its proliferation. Absolute quantification revealed a 4-NQO-induced increase in total bacterial load in the oral cavity, accompanied by elevated absolute abundance of Lactococcus. Unexpectedly, oral administration of Lactococcus strains isolated from 4-NQO-treated mice mildly alleviated inflammation. In vitro, lysates from these strains exhibited protein-dependent cytotoxicity against murine OSCC cells. These results suggest that Lactococcus strains may exert protective effects during OSCC progression.

## Linked entities

- **Chemicals:** 4-nitroquinoline N-oxide (PubChem CID 5955), 4-NQO (PubChem CID 5955)
- **Diseases:** oral squamous cell carcinoma (MONDO:0004958)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** inflammation (MESH:D007249), Dysbiosis (MESH:D064806), cytotoxicity (MESH:D064420), OSCC (MESH:D000077195)
- **Chemicals:** 4-NQO (MESH:D015112)
- **Species:** gut metagenome (species) [taxon 749906], Lactococcus (lactic streptococci, genus) [taxon 1357], Mus musculus (house mouse, species) [taxon 10090]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13013838/full.md

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Source: https://tomesphere.com/paper/PMC13013838