# Dissecting the role of epigenetic regulation in oral squamous cell carcinoma microenvironment: mechanisms and therapeutics

**Authors:** Xuechao Li, Yifei Ren, Shenghua Pei, Kai Zhao, Guanyu Chen, Zhenglin He

PMC · DOI: 10.3389/fimmu.2026.1758433 · Frontiers in Immunology · 2026-01-26

## TL;DR

This paper reviews how epigenetic changes in oral cancer cells and their surrounding environment contribute to tumor growth and resistance to treatment, and explores new therapeutic approaches targeting these changes.

## Contribution

The paper provides a comprehensive review of epigenetic mechanisms in the tumor microenvironment of oral squamous cell carcinoma and their therapeutic implications.

## Key findings

- Epigenetic mechanisms like DNA methylation and non-coding RNAs drive tumor progression and therapy resistance in OSCC.
- Epigenetic drugs and engineered extracellular vesicles show therapeutic potential in targeting OSCC.
- Combining epigenetic therapies with conventional treatments may improve clinical outcomes in OSCC patients.

## Abstract

Oral squamous cell carcinoma (OSCC) is a prevalent and aggressive malignancy with a persistently high mortality rate, largely attributable to therapy resistance and tumor recurrence. This review comprehensively explores the critical interplay between epigenetic dysregulation and the tumor microenvironment (TME) in driving OSCC progression. We detail how key epigenetic mechanisms, including DNA methylation, histone modifications, and non-coding RNAs (ncRNAs), intrinsically transform cancer cells and actively orchestrate pro-tumorigenic TME. These alterations substantially contribute to resistance against conventional therapies. Furthermore, we discuss the therapeutic potential of targeting these pathways using epigenetic drugs (epi-drugs), such as DNA methyltransferase (DNMT) inhibitors and histone deacetylase (HDAC) inhibitors, as well as engineered extracellular vesicles (EVs). The primary objective of this review is to synthesize current knowledge on the epigenetic-TME axis, thereby providing a mechanistic foundation for developing novel therapeutic strategies. We emphasize that rational combinations of epigenetic-targeting agents with conventional treatments or immunotherapy hold significant promise for overcoming drug resistance and improving clinical outcomes in OSCC patients.

## Linked entities

- **Diseases:** oral squamous cell carcinoma (MONDO:0004958)

## Full-text entities

- **Genes:** DNMT1 (DNA methyltransferase 1) [NCBI Gene 1786] {aka ADCADN, AIM, CXXC9, DNMT, HSN1E, MCMT}, HDAC9 (histone deacetylase 9) [NCBI Gene 9734] {aka HD7, HD7b, HD9, HDAC, HDAC7B, HDAC9B}
- **Diseases:** OSCC (MESH:D000077195), cancer (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12883837/full.md

## References

259 references — full list in the complete paper: https://tomesphere.com/paper/PMC12883837/full.md

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Source: https://tomesphere.com/paper/PMC12883837