# Human Papillomavirus: Possible Mechanisms of Damage in Sinonasal Inverted Papilloma

**Authors:** Ana Karla Guzmán-Romero, Rebeca Pérez Cabeza de Vaca, Giovani Visoso-Carvajal, Moises Lopez-Gonzalez, Carmen Selene García-Romero, Jazmín García-Machorro

PMC · DOI: 10.3390/ijms27010245 · International Journal of Molecular Sciences · 2025-12-25

## TL;DR

This paper explores how human papillomavirus might contribute to damage and recurrence in a rare nasal tumor called sinonasal inverted papilloma.

## Contribution

The study highlights new insights into HPV's role in tumor progression and recurrence through immune cell infiltration and epigenetic changes.

## Key findings

- HPV-positive cases show a higher risk of malignancy and recurrence in sinonasal inverted papilloma.
- Tumor microenvironment features include immune cell infiltration and elevated metalloproteinases like MMP-2 and MMP-9.
- Epigenetic alterations are associated with HPV infection in these tumors.

## Abstract

Sinonasal inverted papilloma (SNIP) is a benign neoplasm derived from the Schneiderian membrane and the endoderm of the ciliated respiratory epithelium of the nasal cavity and paranasal sinuses. SNIP is uncommon and typically found between the fourth and seventh decades of life, with men being more frequently affected. The medical significance of this benign neoplasm lies in its potential to cause local tissue destruction, tendency toward malignancy, and high recurrence rate. This study describes the histology of the nasosinusal mucosa and histological characteristics of SNIP, as well as its clinical manifestations and treatment. We also describe findings in the development of SNIP such as chronic inflammation and environmental factors. Additionally, we describe the association between cases positive for the human papillomavirus (HPV) and progression to malignancy and recurrence. This analysis includes the tumor microenvironment, encompassing the infiltration of immune cells such as CD4+ and CD8+ lymphocytes, macrophage polarization, and increases in certain metalloproteinases (MMP-2 and MMP-9). Finally, we address epigenetic alterations associated with HPV infection.

## Linked entities

- **Proteins:** MMP2 (matrix metallopeptidase 2), MMP9 (matrix metallopeptidase 9)

## Full-text entities

- **Genes:** CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, MMP2 (matrix metallopeptidase 2) [NCBI Gene 4313] {aka CLG4, CLG4A, MMP-2, MMP-II, MONA, TBE-1}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}
- **Diseases:** inflammation (MESH:D007249), benign neoplasm (MESH:D009369), SNIP (MESH:D018308)
- **Species:** Human papillomavirus (species) [taxon 10566], Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12786148/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12786148/full.md

## References

74 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786148/full.md

---
Source: https://tomesphere.com/paper/PMC12786148